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	<updated>2026-04-18T06:08:38Z</updated>
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	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=%E6%B3%AE%E6%89%98%E6%8B%89%E5%94%91&amp;diff=5090</id>
		<title>泮托拉唑</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=%E6%B3%AE%E6%89%98%E6%8B%89%E5%94%91&amp;diff=5090"/>
		<updated>2025-01-12T05:37:25Z</updated>

		<summary type="html">&lt;p&gt;Annayung: /* 用藥注意事項 */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]][[Category: 質子泵抑制劑 (PPI)]][[:Category: 胃腸藥 | &#039;&#039;&#039;胃腸藥&#039;&#039;&#039;]] &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Drug class: [[:Category: 質子泵抑制劑 (PPI) | 質子泵抑制劑 (PPI)]]&#039;&#039;&#039; &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;泮托拉唑&#039;&#039;&#039; (English: [[Pantoprazole (PANTOLOC)]]) &lt;br /&gt;
&lt;br /&gt;
==藥物類別== &lt;br /&gt;
&lt;br /&gt;
質子泵抑制劑 (PPI) &lt;br /&gt;
&lt;br /&gt;
==常見劑量== &lt;br /&gt;
&lt;br /&gt;
*20 毫克延遲釋放口服片 &lt;br /&gt;
&lt;br /&gt;
*40 毫克延遲釋放口服片 &lt;br /&gt;
&lt;br /&gt;
*靜脈注射 (IV) 配方 &lt;br /&gt;
&lt;br /&gt;
==藥物商品名稱== &lt;br /&gt;
&lt;br /&gt;
PANTOLOC &lt;br /&gt;
&lt;br /&gt;
==藥物用途== &lt;br /&gt;
&lt;br /&gt;
治療胃潰瘍、十二指腸潰瘍&lt;br /&gt;
&lt;br /&gt;
治療胃食道逆流症（GERD）&lt;br /&gt;
&lt;br /&gt;
預防因使用非類固醇抗炎藥 (NSAIDs) 而導致的胃損傷 &lt;br /&gt;
&lt;br /&gt;
佐林格-埃利森症候群（及其他分泌過多的病症）&lt;br /&gt;
&lt;br /&gt;
根除幽門螺旋桿菌&lt;br /&gt;
&lt;br /&gt;
==作用機制== &lt;br /&gt;
&lt;br /&gt;
通過不可逆地結合到胃壁細胞中的 H+/K+ ATPase 酶，從而有效抑制胃酸生成的最終步驟，導致胃內酸分泌減少。 &lt;br /&gt;
&lt;br /&gt;
==給藥途徑== &lt;br /&gt;
&lt;br /&gt;
口服 &lt;br /&gt;
&lt;br /&gt;
靜脈注射（注射） &lt;br /&gt;
&lt;br /&gt;
==劑量== &lt;br /&gt;
&lt;br /&gt;
胃潰瘍、十二指腸潰瘍：靜脈注射 40 毫克，直至恢復口服為止&lt;br /&gt;
&lt;br /&gt;
胃潰瘍、十二指腸潰瘍：口服，每日 40 毫克；如有必要，每日增加至 80 毫克&lt;br /&gt;
&lt;br /&gt;
胃食道逆流症：每天20至80毫克，持續4週，如果未完全癒合，則繼續持續4週，早上服用；維持劑量每天 20 毫克，如症狀恢復時，可增加至每天 40 毫克&lt;br /&gt;
&lt;br /&gt;
預防 NSAID 相關潰瘍：每天 20 毫克&lt;br /&gt;
&lt;br /&gt;
佐林格-埃利森症候群（和其他分泌過多的病症）：最初每天 80 毫克，根據反應調整&lt;br /&gt;
&lt;br /&gt;
根除幽門螺旋桿菌：40 毫克，每日兩次&lt;br /&gt;
&lt;br /&gt;
對於腎功能受損的患者，根據 eGFR 通常不需要特定劑量調整，但建議謹慎使用。 &lt;br /&gt;
&lt;br /&gt;
==副作用== &lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot; &lt;br /&gt;
 !style=&amp;quot;text-align: left&amp;quot;| 頻率 &lt;br /&gt;
 !不良反應 &lt;br /&gt;
|- &lt;br /&gt;
| rowspan=6 | &#039;&#039;&#039;常見副作用包括： &lt;br /&gt;
|- &lt;br /&gt;
| 腹瀉 &lt;br /&gt;
|- &lt;br /&gt;
| 腹痛 &lt;br /&gt;
|- &lt;br /&gt;
| 噁心 &lt;br /&gt;
|- &lt;br /&gt;
| 嘔吐 &lt;br /&gt;
|- &lt;br /&gt;
| 腹脹 &lt;br /&gt;
|- &lt;br /&gt;
| rowspan=6 | &#039;&#039;&#039;長期使用的嚴重副包括： &lt;br /&gt;
|- &lt;br /&gt;
| 骨質疏鬆症相關的骨折 &lt;br /&gt;
|- &lt;br /&gt;
| 低血鎂水平（低鎂血症） &lt;br /&gt;
|- &lt;br /&gt;
| 急性間質性腎炎 &lt;br /&gt;
|- &lt;br /&gt;
| 艱難梭菌感染 &lt;br /&gt;
|- &lt;br /&gt;
| 維生素B12缺乏症 &lt;br /&gt;
|} &lt;br /&gt;
==藥物動力學== &lt;br /&gt;
&lt;br /&gt;
起效時間：口服後約 2 至 3 小時可觀察到效果。 &lt;br /&gt;
&lt;br /&gt;
作用持續時間：胃酸抑制效果持續約 24 小時。 &lt;br /&gt;
&lt;br /&gt;
==用藥注意事項== &lt;br /&gt;
&lt;br /&gt;
懷孕：除非潛在益處大於風險，否則避免服用&lt;br /&gt;
&lt;br /&gt;
哺乳：除非潛在益處大於風險，否則避免服用&lt;br /&gt;
&lt;br /&gt;
兒童和老年人：5歲以上兒童使用一般是安全的；老年患者可能需要監測，因為骨折、腎臟問題和艱難梭菌感染等副作用的風險可能增加。&lt;br /&gt;
&lt;br /&gt;
監測項目：定期監測鎂和維生素 B12 水平 &lt;br /&gt;
&lt;br /&gt;
藥物相互作用：主要透過兩種機制與其他藥物交互作用：&lt;br /&gt;
*改變胃部 pH 值：泮托拉唑會增加胃部 pH 值，從而影響需要酸性環境吸收的藥物的溶解度和吸收。例如，酮康唑和阿扎那韋等藥物與 PPI 一起服用時，由於 pH 值的改變，生物利用度顯著降低。&lt;br /&gt;
*細胞色素 P450 酶的抑制：這可能導致通過這些途徑代謝的藥物血漿濃度增加。這對於華法林、氯吡格雷和某些抗癲癇藥物（如苯妥英）等藥物尤其重要。&lt;br /&gt;
*甲胺蝶呤：泮托拉唑會影響甲胺蝶呤的藥物動力學，可能導致毒性增加。&lt;br /&gt;
&lt;br /&gt;
主要藥物交互作用總結：&lt;br /&gt;
*氯吡格雷：有效性降低；導致心血管風險增加&lt;br /&gt;
*華法林：增強抗凝血作用；監測INR&lt;br /&gt;
*甲胺蝶呤：增加毒性風險；監測腎功能&lt;br /&gt;
*苯妥英：改變新陳代謝；監測藥物水平&lt;br /&gt;
*阿扎那韋：生物利用度降低；考慮替代方案&lt;br /&gt;
&lt;br /&gt;
==常見問題== &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;我應該如何服用這種藥片？ &lt;br /&gt;
&lt;br /&gt;
在餐前服用 Pantoprazole，整片吞下，不要壓碎或咀嚼。 &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;服用時應避免什麼？ &lt;br /&gt;
&lt;br /&gt;
限製或避免高酸性食物和咖啡、蘇打水等飲料 &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;如果我錯過一劑怎麼辦？ &lt;br /&gt;
&lt;br /&gt;
請儘快服用。如果距離下一劑時間已近，則跳過錯過的劑量，請勿重複服用。&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=%E6%B3%AE%E6%89%98%E6%8B%89%E5%94%91&amp;diff=5089</id>
		<title>泮托拉唑</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=%E6%B3%AE%E6%89%98%E6%8B%89%E5%94%91&amp;diff=5089"/>
		<updated>2025-01-12T05:36:24Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]][[Category: 質子泵抑制劑 (PPI)]][[:Category: 胃腸藥 | &#039;&#039;&#039;胃腸藥&#039;&#039;&#039;]] &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Drug class: [[:Category: 質子泵抑制劑 (PPI) | 質子泵抑制劑 (PPI)]]&#039;&#039;&#039; &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;泮托拉唑&#039;&#039;&#039; (English: [[Pantoprazole (PANTOLOC)]]) &lt;br /&gt;
&lt;br /&gt;
==藥物類別== &lt;br /&gt;
&lt;br /&gt;
質子泵抑制劑 (PPI) &lt;br /&gt;
&lt;br /&gt;
==常見劑量== &lt;br /&gt;
&lt;br /&gt;
*20 毫克延遲釋放口服片 &lt;br /&gt;
&lt;br /&gt;
*40 毫克延遲釋放口服片 &lt;br /&gt;
&lt;br /&gt;
*靜脈注射 (IV) 配方 &lt;br /&gt;
&lt;br /&gt;
==藥物商品名稱== &lt;br /&gt;
&lt;br /&gt;
PANTOLOC &lt;br /&gt;
&lt;br /&gt;
==藥物用途== &lt;br /&gt;
&lt;br /&gt;
治療胃潰瘍、十二指腸潰瘍&lt;br /&gt;
&lt;br /&gt;
治療胃食道逆流症（GERD）&lt;br /&gt;
&lt;br /&gt;
預防因使用非類固醇抗炎藥 (NSAIDs) 而導致的胃損傷 &lt;br /&gt;
&lt;br /&gt;
佐林格-埃利森症候群（及其他分泌過多的病症）&lt;br /&gt;
&lt;br /&gt;
根除幽門螺旋桿菌&lt;br /&gt;
&lt;br /&gt;
==作用機制== &lt;br /&gt;
&lt;br /&gt;
通過不可逆地結合到胃壁細胞中的 H+/K+ ATPase 酶，從而有效抑制胃酸生成的最終步驟，導致胃內酸分泌減少。 &lt;br /&gt;
&lt;br /&gt;
==給藥途徑== &lt;br /&gt;
&lt;br /&gt;
口服 &lt;br /&gt;
&lt;br /&gt;
靜脈注射（注射） &lt;br /&gt;
&lt;br /&gt;
==劑量== &lt;br /&gt;
&lt;br /&gt;
胃潰瘍、十二指腸潰瘍：靜脈注射 40 毫克，直至恢復口服為止&lt;br /&gt;
&lt;br /&gt;
胃潰瘍、十二指腸潰瘍：口服，每日 40 毫克；如有必要，每日增加至 80 毫克&lt;br /&gt;
&lt;br /&gt;
胃食道逆流症：每天20至80毫克，持續4週，如果未完全癒合，則繼續持續4週，早上服用；維持劑量每天 20 毫克，如症狀恢復時，可增加至每天 40 毫克&lt;br /&gt;
&lt;br /&gt;
預防 NSAID 相關潰瘍：每天 20 毫克&lt;br /&gt;
&lt;br /&gt;
佐林格-埃利森症候群（和其他分泌過多的病症）：最初每天 80 毫克，根據反應調整&lt;br /&gt;
&lt;br /&gt;
根除幽門螺旋桿菌：40 毫克，每日兩次&lt;br /&gt;
&lt;br /&gt;
對於腎功能受損的患者，根據 eGFR 通常不需要特定劑量調整，但建議謹慎使用。 &lt;br /&gt;
&lt;br /&gt;
==副作用== &lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot; &lt;br /&gt;
 !style=&amp;quot;text-align: left&amp;quot;| 頻率 &lt;br /&gt;
 !不良反應 &lt;br /&gt;
|- &lt;br /&gt;
| rowspan=6 | &#039;&#039;&#039;常見副作用包括： &lt;br /&gt;
|- &lt;br /&gt;
| 腹瀉 &lt;br /&gt;
|- &lt;br /&gt;
| 腹痛 &lt;br /&gt;
|- &lt;br /&gt;
| 噁心 &lt;br /&gt;
|- &lt;br /&gt;
| 嘔吐 &lt;br /&gt;
|- &lt;br /&gt;
| 腹脹 &lt;br /&gt;
|- &lt;br /&gt;
| rowspan=6 | &#039;&#039;&#039;長期使用的嚴重副包括： &lt;br /&gt;
|- &lt;br /&gt;
| 骨質疏鬆症相關的骨折 &lt;br /&gt;
|- &lt;br /&gt;
| 低血鎂水平（低鎂血症） &lt;br /&gt;
|- &lt;br /&gt;
| 急性間質性腎炎 &lt;br /&gt;
|- &lt;br /&gt;
| 艱難梭菌感染 &lt;br /&gt;
|- &lt;br /&gt;
| 維生素B12缺乏症 &lt;br /&gt;
|} &lt;br /&gt;
==藥物動力學== &lt;br /&gt;
&lt;br /&gt;
起效時間：口服後約 2 至 3 小時可觀察到效果。 &lt;br /&gt;
&lt;br /&gt;
作用持續時間：胃酸抑制效果持續約 24 小時。 &lt;br /&gt;
&lt;br /&gt;
==用藥注意事項== &lt;br /&gt;
&lt;br /&gt;
懷孕：除非潛在益處大於風險，否則避免服用&lt;br /&gt;
&lt;br /&gt;
哺乳：除非潛在益處大於風險，否則避免服用。 &lt;br /&gt;
&lt;br /&gt;
兒童和老年人：5歲以上兒童使用一般是安全的；老年患者可能需要監測，因為骨折、腎臟問題和艱難梭菌感染等副作用的風險可能增加。&lt;br /&gt;
&lt;br /&gt;
監測項目：定期監測鎂和維生素 B12 水平 &lt;br /&gt;
&lt;br /&gt;
藥物相互作用：主要透過兩種機制與其他藥物交互作用：&lt;br /&gt;
*改變胃部 pH 值：泮托拉唑會增加胃部 pH 值，從而影響需要酸性環境吸收的藥物的溶解度和吸收。例如，酮康唑和阿扎那韋等藥物與 PPI 一起服用時，由於 pH 值的改變，生物利用度顯著降低。&lt;br /&gt;
*細胞色素 P450 酶的抑制：這可能導致通過這些途徑代謝的藥物血漿濃度增加。這對於華法林、氯吡格雷和某些抗癲癇藥物（如苯妥英）等藥物尤其重要。&lt;br /&gt;
*甲胺蝶呤：泮托拉唑會影響甲胺蝶呤的藥物動力學，可能導致毒性增加。&lt;br /&gt;
&lt;br /&gt;
主要藥物交互作用總結：&lt;br /&gt;
*氯吡格雷：有效性降低；導致心血管風險增加&lt;br /&gt;
*華法林：增強抗凝血作用；監測INR&lt;br /&gt;
*甲胺蝶呤：增加毒性風險；監測腎功能&lt;br /&gt;
*苯妥英：改變新陳代謝；監測藥物水平&lt;br /&gt;
*阿扎那韋：生物利用度降低；考慮替代方案&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==常見問題== &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;我應該如何服用這種藥片？ &lt;br /&gt;
&lt;br /&gt;
在餐前服用 Pantoprazole，整片吞下，不要壓碎或咀嚼。 &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;服用時應避免什麼？ &lt;br /&gt;
&lt;br /&gt;
限製或避免高酸性食物和咖啡、蘇打水等飲料 &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;如果我錯過一劑怎麼辦？ &lt;br /&gt;
&lt;br /&gt;
請儘快服用。如果距離下一劑時間已近，則跳過錯過的劑量，請勿重複服用。&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Pantoprazole_(PANTOLOC)&amp;diff=5088</id>
		<title>Pantoprazole (PANTOLOC)</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Pantoprazole_(PANTOLOC)&amp;diff=5088"/>
		<updated>2025-01-12T04:47:20Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]][[Category: Proton Pump Inhibitors (PPI)]][[:Category: Gastrointestinal Drug | &#039;&#039;&#039;Gastrointestinal Drug&#039;&#039;&#039;]] &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Drug class: [[:Category: Proton Pump Inhibitors (PPI) | Proton Pump Inhibitors (PPI)]]&#039;&#039;&#039; &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Pantoprazole&#039;&#039;&#039; (中文: [[泮托拉唑]]) &lt;br /&gt;
&lt;br /&gt;
==Drug Class== &lt;br /&gt;
&lt;br /&gt;
Proton Pump Inhibitor (PPI) &lt;br /&gt;
&lt;br /&gt;
==Common Strengths of Pantoprazole tablet== &lt;br /&gt;
&lt;br /&gt;
Pantoprazole tablets are available in the following strengths: &lt;br /&gt;
&lt;br /&gt;
*20 mg delayed-release oral tablets &lt;br /&gt;
&lt;br /&gt;
*40 mg delayed-release oral tablets &lt;br /&gt;
&lt;br /&gt;
*Intravenous (IV) formulation for injection &lt;br /&gt;
&lt;br /&gt;
==Drug Trade Name of Pantoprazole tablet== &lt;br /&gt;
&lt;br /&gt;
PANTOLOC &lt;br /&gt;
&lt;br /&gt;
==Drug Usage== &lt;br /&gt;
&lt;br /&gt;
Pantoprazole is used for: &lt;br /&gt;
&lt;br /&gt;
Gastric ulcer, duodenal ulcer &lt;br /&gt;
&lt;br /&gt;
Treatment of gastroesophageal reflux disease (GERD) &lt;br /&gt;
&lt;br /&gt;
Prevention of gastric damage in patients taking NSAIDs&lt;br /&gt;
&lt;br /&gt;
Zollinger-Ellison syndrome (and other hypersecretory conditions)&lt;br /&gt;
&lt;br /&gt;
Eradication of Helicobacter pylori  &lt;br /&gt;
&lt;br /&gt;
==Mechanism of Action== &lt;br /&gt;
&lt;br /&gt;
Inhibits (H+/K+ )-ATPase enzyme in the gastric parietal cells, blocking the final step of gastric acid production in the stomach, significantly reducing gastric acidity for up to 24 hours or more. &lt;br /&gt;
&lt;br /&gt;
==Route of Administration== &lt;br /&gt;
&lt;br /&gt;
Oral and intravenously (injection) &lt;br /&gt;
&lt;br /&gt;
==Dosages == &lt;br /&gt;
&lt;br /&gt;
Gastric ulcer, duodenal ulcer: By intravenous injection, or by intravenous infusion 40mg daily until oral administration can be resumed&lt;br /&gt;
&lt;br /&gt;
Gastric ulcer, duodenal ulcer: By mouth, 40 mg daily; increased if necessary up to 80mg daily&lt;br /&gt;
&lt;br /&gt;
GERD: 20-80 mg daily for 4 weeks, continue for further 4 weeks if not fully healed, dose to be taken in the morning; maintenance 20 mg daily and increased to 40 mg daily, increased only if symptoms return&lt;br /&gt;
&lt;br /&gt;
Propylaxis of NSAID-associated ulcer: 20 mg daily&lt;br /&gt;
&lt;br /&gt;
Zollinger-Ellison syndrome (and other hypersecretory conditions): intially 80 mg daily, adjusted according to response&lt;br /&gt;
&lt;br /&gt;
Helicobacter pylori eradication: 40 mg twice daily&lt;br /&gt;
&lt;br /&gt;
==Renal Dose Adjustments== &lt;br /&gt;
&lt;br /&gt;
There are no specific renal dose adjustments recommended based on the estimated glomerular filtration rate (eGFR) for pantoprazole; however, caution should be exercised in severe renal impairment. &lt;br /&gt;
&lt;br /&gt;
==Side Effects== &lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot; &lt;br /&gt;
 !style=&amp;quot;text-align: left&amp;quot;| Frequency &lt;br /&gt;
 !Adverse reactions &lt;br /&gt;
|- &lt;br /&gt;
| rowspan=6 | &#039;&#039;&#039;Common Side Effects &lt;br /&gt;
|- &lt;br /&gt;
| Diarrhea &lt;br /&gt;
|- &lt;br /&gt;
| Abdominal pain &lt;br /&gt;
|- &lt;br /&gt;
| Nausea &lt;br /&gt;
|- &lt;br /&gt;
| Vomiting &lt;br /&gt;
|- &lt;br /&gt;
| Flatulence &lt;br /&gt;
|- &lt;br /&gt;
| rowspan=5 | &#039;&#039;&#039;Serious Side Effects of long-term use&lt;br /&gt;
|- &lt;br /&gt;
| Osteoporosis-related fractures &lt;br /&gt;
|- &lt;br /&gt;
| Clostridium difficile infection &lt;br /&gt;
|- &lt;br /&gt;
| Low blood magnesium and Vit B12&lt;br /&gt;
|- &lt;br /&gt;
| Acute Interstitial Nephritis&lt;br /&gt;
|} &lt;br /&gt;
==Pharmacokinetics== &lt;br /&gt;
&lt;br /&gt;
Onset Time: Effects can be observed within 2 to 3 hours after oral administration. &lt;br /&gt;
&lt;br /&gt;
Duration of Action: The acid-suppressive effect lasts approximately 24 hours. &lt;br /&gt;
&lt;br /&gt;
==Drug Precautions== &lt;br /&gt;
&lt;br /&gt;
Pregnancy: avoid unless the potential benefit outweighs risk&lt;br /&gt;
&lt;br /&gt;
Breastfeeding: void unless the potential benefit outweighs risk &lt;br /&gt;
&lt;br /&gt;
Children and Elderly: Use in children over 5 years is generally safe; elderly patients may require monitoring due to the potential increased risk of side effects such as bone fractures, kidney problems, and Clostridium difficile infection.&lt;br /&gt;
&lt;br /&gt;
==Monitoring Items== &lt;br /&gt;
&lt;br /&gt;
Regular monitoring of magnesium and vitamin B12 levels &lt;br /&gt;
&lt;br /&gt;
==Drug Interactions== &lt;br /&gt;
&lt;br /&gt;
Drug Interactions: can interact with other medications primarily through two mechanisms:&lt;br /&gt;
*Alteration of Gastric pH: Pantoprazole increases gastric pH, which can affect the solubility and absorption of drugs that require an acidic environment for optimal absorption. For example, drugs like ketoconazole and atazanavir have significantly reduced bioavailability when taken with PPIs due to this pH alteration.&lt;br /&gt;
*Inhibition of Cytochrome P450 Enzymes: which can lead to increased plasma concentrations of drugs metabolized by these pathways. This is particularly relevant for medications such as warfarin, clopidogrel, and certain antiepileptics like phenytoin.&lt;br /&gt;
*Methotrexate: Pantoprazole can affect the pharmacokinetics of methotrexate, potentially leading to increased toxicity.&lt;br /&gt;
Summary of Key Drug Interactions:&lt;br /&gt;
*Clopidogrel: Reduced effectiveness; increased cardiovascular risk&lt;br /&gt;
*Warfarin: Increased anticoagulation effect; monitor INR&lt;br /&gt;
*Methotrexate: Increased toxicity risk; monitor renal function&lt;br /&gt;
*Phenytoin: Altered metabolism; monitor drug levels.&lt;br /&gt;
*Atazanavir: Reduced bioavailability; consider alternatives&lt;br /&gt;
&lt;br /&gt;
==FAQ== &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;How should I take the tablet? &lt;br /&gt;
&lt;br /&gt;
Take pantoprazole on an empty stomach, ideally 30 minutes before meals, swallowing the tablet whole without crushing or chewing. Consuming them with food may reduce their effectiveness.&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;What should I avoid while taking? &lt;br /&gt;
&lt;br /&gt;
Limit or avoid highly acidic foods and drinks like coffee and soda &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;What happens if I miss a dose? &lt;br /&gt;
&lt;br /&gt;
Take as soon as remembered unless close to next dose; do not double up on doses&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5033</id>
		<title>Rabeprazole</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5033"/>
		<updated>2025-01-05T14:44:22Z</updated>

		<summary type="html">&lt;p&gt;Annayung: /* Dosages for Normal People */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
= Rabeprazole =&lt;br /&gt;
==Pronunciation==&lt;br /&gt;
===Rabeprazole 20mg===&lt;br /&gt;
[[File:Rabeprazole 20mg.mp3]]&lt;br /&gt;
&lt;br /&gt;
== Drug Class ==&lt;br /&gt;
Rabeprazole belongs to the class of medications known as &#039;&#039;&#039;proton pump inhibitors (PPIs)&#039;&#039;&#039;. These drugs work by inhibiting gastric acid secretion.&lt;br /&gt;
&lt;br /&gt;
== Common Strengths ==&lt;br /&gt;
Rabeprazole is available in the following strengths:&lt;br /&gt;
* 10 mg delayed-release tablets&lt;br /&gt;
* 20 mg delayed-release tablets&lt;br /&gt;
&lt;br /&gt;
== Drug Trade Name ==&lt;br /&gt;
Rabeprazole is marketed under the trade name &#039;&#039;&#039;PARIET&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Drug Usage ==&lt;br /&gt;
Rabeprazole is primarily used for:&lt;br /&gt;
* Healing of erosive or ulcerative gastroesophageal reflux disease (GERD)&lt;br /&gt;
* Maintenance of healing of erosive or ulcerative GERD&lt;br /&gt;
* Treatment of symptomatic GERD&lt;br /&gt;
* Healing of duodenal ulcers&lt;br /&gt;
* Eradication of &#039;&#039;Helicobacter pylori&#039;&#039; to reduce the risk of duodenal ulcer recurrence&lt;br /&gt;
* Treatment of pathological hypersecretory conditions, including Zollinger-Ellison syndrome&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Rabeprazole works by selectively and irreversibly inhibiting the H^+, K^+-ATPase enzyme system (the proton pump) at the secretory surface of gastric parietal cells. This inhibition reduces gastric acid secretion, thereby alleviating symptoms associated with excess stomach acid.&lt;br /&gt;
&lt;br /&gt;
== Route of Administration ==&lt;br /&gt;
Rabeprazole is administered orally, available as delayed-release tablets.&lt;br /&gt;
&lt;br /&gt;
== Dosages ==&lt;br /&gt;
The typical dosage for adults is:&lt;br /&gt;
* &#039;&#039;&#039;GERD treatment:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks; maintenance 10-20 mg daily.&lt;br /&gt;
* &#039;&#039;&#039;Benign gastric ulcer:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks, dose to be taken in the morning.&lt;br /&gt;
* &#039;&#039;&#039;Duodenal ulcer:&#039;&#039;&#039; 20 mg once daily for 4 weeks, dose to be taken in the morning.&lt;br /&gt;
* &#039;&#039;&#039;Zollinger-Ellison syndrome:&#039;&#039;&#039; Initially 60 mg once daily, adjusted according to response, doses above 100 mg daily given in 2 divided doses; maximum 120 mg per day.&lt;br /&gt;
* &#039;&#039;&#039;H. pylori eradication:&#039;&#039;&#039; 20 mg twice daily.&lt;br /&gt;
&lt;br /&gt;
For renal dosing based on eGFR:&lt;br /&gt;
* No specific renal dose adjustment is typically required, but caution is advised in patients with severe renal impairment.&lt;br /&gt;
&lt;br /&gt;
== Side-Effects: Common and Serious Side Effects ==&lt;br /&gt;
Common side-effects may include:&lt;br /&gt;
* Constipation&lt;br /&gt;
* Cough&lt;br /&gt;
* Influenza like syndrome&lt;br /&gt;
&lt;br /&gt;
Serious side-effects may include:&lt;br /&gt;
* Increased Osteoporosis-related fractures, particularly in older adults&lt;br /&gt;
* Low blood magnesium levels&lt;br /&gt;
* &#039;&#039;Clostridium difficile&#039;&#039; infection in the colon&lt;br /&gt;
* Acute Tubulointerstitial Nephritis can manifest as decreased urine output or blood in the urine&lt;br /&gt;
* Vitamin B12 Deficiency: Symptoms include fatigue, sore tongue, and neurological issues&lt;br /&gt;
&lt;br /&gt;
==Pharmacokinetics==&lt;br /&gt;
It undergoes hepatic metabolism and has a half-life of about 1 to 2 hours. The onset of action occurs within 1 hour, with a duration of action lasting up to 24 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Precautions ==&lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
The safety of rabeprazole during pregnancy is unclear; it should only be used if clearly needed.&lt;br /&gt;
&lt;br /&gt;
=== Breastfeeding ===&lt;br /&gt;
It is unknown whether rabeprazole passes into breast milk; caution is advised.&lt;br /&gt;
&lt;br /&gt;
=== Children and Elderly ===&lt;br /&gt;
Rabeprazole can be used in children aged 12 years and older for GERD treatment. Use in elderly patients may require careful monitoring due to potential increased sensitivity to side effects.&lt;br /&gt;
&lt;br /&gt;
=== Monitoring Items ===&lt;br /&gt;
Patients on rabeprazole should be monitored for:&lt;br /&gt;
* Signs of gastrointestinal bleeding&lt;br /&gt;
* Electrolyte levels, particularly magnesium&lt;br /&gt;
&lt;br /&gt;
=== Drug Interactions ===&lt;br /&gt;
Rabeprazole may interact with other medications, including:&lt;br /&gt;
* HIV Medications: Atazanavir, nelfinavir, and rilpivirine by reducing the absorption and effectiveness of these antiretroviral drugs, which may lead to treatment failure and resistance development.&lt;br /&gt;
* Clopidogrel: Rabeprazole may reduce the effectiveness of clopidogrel, a blood thinner, potentially increasing the risk of cardiovascular events.&lt;br /&gt;
* Itraconazole and ketoconazole: The absorption of these antifungal agents may be decreased when taken with rabeprazole due to altered gastric pH.&lt;br /&gt;
* Methotrexate: Concurrent use can lead to increased levels of methotrexate in the body, raising the risk of serious side effects such as kidney damage and anemia.&lt;br /&gt;
* Digoxin: Rabeprazole can increase the serum levels of digoxin, which is used to treat heart conditions, necessitating careful monitoring.&lt;br /&gt;
* St. John&#039;s Wort: This herbal supplement can reduce the effectiveness of rabeprazole by inducing hepatic enzymes that metabolize the drug.&lt;br /&gt;
&lt;br /&gt;
== FAQ ==&lt;br /&gt;
&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
Take rabeprazole orally, usually once daily before a meal. Swallow the tablet whole without crushing or chewing.&lt;br /&gt;
&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid concomitant use with certain medications like iron supplements and St. John&#039;s wort.&lt;br /&gt;
&lt;br /&gt;
=== What happens if I miss a dose? ===&lt;br /&gt;
If you miss a dose, take it as soon as you remember. If it&#039;s almost time for your next dose, skip the missed dose and resume your regular schedule. Do not double the dose.&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5032</id>
		<title>Rabeprazole</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5032"/>
		<updated>2025-01-05T14:43:25Z</updated>

		<summary type="html">&lt;p&gt;Annayung: /* Pharmacokinetics */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
= Rabeprazole =&lt;br /&gt;
==Pronunciation==&lt;br /&gt;
===Rabeprazole 20mg===&lt;br /&gt;
[[File:Rabeprazole 20mg.mp3]]&lt;br /&gt;
&lt;br /&gt;
== Drug Class ==&lt;br /&gt;
Rabeprazole belongs to the class of medications known as &#039;&#039;&#039;proton pump inhibitors (PPIs)&#039;&#039;&#039;. These drugs work by inhibiting gastric acid secretion.&lt;br /&gt;
&lt;br /&gt;
== Common Strengths ==&lt;br /&gt;
Rabeprazole is available in the following strengths:&lt;br /&gt;
* 10 mg delayed-release tablets&lt;br /&gt;
* 20 mg delayed-release tablets&lt;br /&gt;
&lt;br /&gt;
== Drug Trade Name ==&lt;br /&gt;
Rabeprazole is marketed under the trade name &#039;&#039;&#039;PARIET&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Drug Usage ==&lt;br /&gt;
Rabeprazole is primarily used for:&lt;br /&gt;
* Healing of erosive or ulcerative gastroesophageal reflux disease (GERD)&lt;br /&gt;
* Maintenance of healing of erosive or ulcerative GERD&lt;br /&gt;
* Treatment of symptomatic GERD&lt;br /&gt;
* Healing of duodenal ulcers&lt;br /&gt;
* Eradication of &#039;&#039;Helicobacter pylori&#039;&#039; to reduce the risk of duodenal ulcer recurrence&lt;br /&gt;
* Treatment of pathological hypersecretory conditions, including Zollinger-Ellison syndrome&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Rabeprazole works by selectively and irreversibly inhibiting the H^+, K^+-ATPase enzyme system (the proton pump) at the secretory surface of gastric parietal cells. This inhibition reduces gastric acid secretion, thereby alleviating symptoms associated with excess stomach acid.&lt;br /&gt;
&lt;br /&gt;
== Route of Administration ==&lt;br /&gt;
Rabeprazole is administered orally, available as delayed-release tablets.&lt;br /&gt;
&lt;br /&gt;
== Dosages for Normal People ==&lt;br /&gt;
The typical dosage for adults is:&lt;br /&gt;
* &#039;&#039;&#039;GERD treatment:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks; maintenance 10-20 mg daily.&lt;br /&gt;
* &#039;&#039;&#039;Benign gastric ulcer:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks, dose to be taken in the morning.&lt;br /&gt;
* &#039;&#039;&#039;Duodenal ulcer:&#039;&#039;&#039; 20 mg once daily for 4 weeks, dose to be taken in the morning.&lt;br /&gt;
* &#039;&#039;&#039;Zollinger-Ellison syndrome:&#039;&#039;&#039; Initially 60 mg once daily, adjusted according to response, doses above 100 mg daily given in 2 divided doses; maximum 120 mg per day.&lt;br /&gt;
* &#039;&#039;&#039;H. pylori eradication:&#039;&#039;&#039; 20 mg twice daily.&lt;br /&gt;
&lt;br /&gt;
For renal dosing based on eGFR:&lt;br /&gt;
* No specific renal dose adjustment is typically required, but caution is advised in patients with severe renal impairment.&lt;br /&gt;
&lt;br /&gt;
== Side-Effects: Common and Serious Side Effects ==&lt;br /&gt;
Common side-effects may include:&lt;br /&gt;
* Constipation&lt;br /&gt;
* Cough&lt;br /&gt;
* Influenza like syndrome&lt;br /&gt;
&lt;br /&gt;
Serious side-effects may include:&lt;br /&gt;
* Increased Osteoporosis-related fractures, particularly in older adults&lt;br /&gt;
* Low blood magnesium levels&lt;br /&gt;
* &#039;&#039;Clostridium difficile&#039;&#039; infection in the colon&lt;br /&gt;
* Acute Tubulointerstitial Nephritis can manifest as decreased urine output or blood in the urine&lt;br /&gt;
* Vitamin B12 Deficiency: Symptoms include fatigue, sore tongue, and neurological issues&lt;br /&gt;
&lt;br /&gt;
==Pharmacokinetics==&lt;br /&gt;
It undergoes hepatic metabolism and has a half-life of about 1 to 2 hours. The onset of action occurs within 1 hour, with a duration of action lasting up to 24 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Precautions ==&lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
The safety of rabeprazole during pregnancy is unclear; it should only be used if clearly needed.&lt;br /&gt;
&lt;br /&gt;
=== Breastfeeding ===&lt;br /&gt;
It is unknown whether rabeprazole passes into breast milk; caution is advised.&lt;br /&gt;
&lt;br /&gt;
=== Children and Elderly ===&lt;br /&gt;
Rabeprazole can be used in children aged 12 years and older for GERD treatment. Use in elderly patients may require careful monitoring due to potential increased sensitivity to side effects.&lt;br /&gt;
&lt;br /&gt;
=== Monitoring Items ===&lt;br /&gt;
Patients on rabeprazole should be monitored for:&lt;br /&gt;
* Signs of gastrointestinal bleeding&lt;br /&gt;
* Electrolyte levels, particularly magnesium&lt;br /&gt;
&lt;br /&gt;
=== Drug Interactions ===&lt;br /&gt;
Rabeprazole may interact with other medications, including:&lt;br /&gt;
* HIV Medications: Atazanavir, nelfinavir, and rilpivirine by reducing the absorption and effectiveness of these antiretroviral drugs, which may lead to treatment failure and resistance development.&lt;br /&gt;
* Clopidogrel: Rabeprazole may reduce the effectiveness of clopidogrel, a blood thinner, potentially increasing the risk of cardiovascular events.&lt;br /&gt;
* Itraconazole and ketoconazole: The absorption of these antifungal agents may be decreased when taken with rabeprazole due to altered gastric pH.&lt;br /&gt;
* Methotrexate: Concurrent use can lead to increased levels of methotrexate in the body, raising the risk of serious side effects such as kidney damage and anemia.&lt;br /&gt;
* Digoxin: Rabeprazole can increase the serum levels of digoxin, which is used to treat heart conditions, necessitating careful monitoring.&lt;br /&gt;
* St. John&#039;s Wort: This herbal supplement can reduce the effectiveness of rabeprazole by inducing hepatic enzymes that metabolize the drug.&lt;br /&gt;
&lt;br /&gt;
== FAQ ==&lt;br /&gt;
&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
Take rabeprazole orally, usually once daily before a meal. Swallow the tablet whole without crushing or chewing.&lt;br /&gt;
&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid concomitant use with certain medications like iron supplements and St. John&#039;s wort.&lt;br /&gt;
&lt;br /&gt;
=== What happens if I miss a dose? ===&lt;br /&gt;
If you miss a dose, take it as soon as you remember. If it&#039;s almost time for your next dose, skip the missed dose and resume your regular schedule. Do not double the dose.&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5031</id>
		<title>Rabeprazole</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5031"/>
		<updated>2025-01-05T14:42:59Z</updated>

		<summary type="html">&lt;p&gt;Annayung: /* Pharmacokinetics */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
= Rabeprazole =&lt;br /&gt;
==Pronunciation==&lt;br /&gt;
===Rabeprazole 20mg===&lt;br /&gt;
[[File:Rabeprazole 20mg.mp3]]&lt;br /&gt;
&lt;br /&gt;
== Drug Class ==&lt;br /&gt;
Rabeprazole belongs to the class of medications known as &#039;&#039;&#039;proton pump inhibitors (PPIs)&#039;&#039;&#039;. These drugs work by inhibiting gastric acid secretion.&lt;br /&gt;
&lt;br /&gt;
== Common Strengths ==&lt;br /&gt;
Rabeprazole is available in the following strengths:&lt;br /&gt;
* 10 mg delayed-release tablets&lt;br /&gt;
* 20 mg delayed-release tablets&lt;br /&gt;
&lt;br /&gt;
== Drug Trade Name ==&lt;br /&gt;
Rabeprazole is marketed under the trade name &#039;&#039;&#039;PARIET&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Drug Usage ==&lt;br /&gt;
Rabeprazole is primarily used for:&lt;br /&gt;
* Healing of erosive or ulcerative gastroesophageal reflux disease (GERD)&lt;br /&gt;
* Maintenance of healing of erosive or ulcerative GERD&lt;br /&gt;
* Treatment of symptomatic GERD&lt;br /&gt;
* Healing of duodenal ulcers&lt;br /&gt;
* Eradication of &#039;&#039;Helicobacter pylori&#039;&#039; to reduce the risk of duodenal ulcer recurrence&lt;br /&gt;
* Treatment of pathological hypersecretory conditions, including Zollinger-Ellison syndrome&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Rabeprazole works by selectively and irreversibly inhibiting the H^+, K^+-ATPase enzyme system (the proton pump) at the secretory surface of gastric parietal cells. This inhibition reduces gastric acid secretion, thereby alleviating symptoms associated with excess stomach acid.&lt;br /&gt;
&lt;br /&gt;
== Route of Administration ==&lt;br /&gt;
Rabeprazole is administered orally, available as delayed-release tablets.&lt;br /&gt;
&lt;br /&gt;
== Dosages for Normal People ==&lt;br /&gt;
The typical dosage for adults is:&lt;br /&gt;
* &#039;&#039;&#039;GERD treatment:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks; maintenance 10-20 mg daily.&lt;br /&gt;
* &#039;&#039;&#039;Benign gastric ulcer:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks, dose to be taken in the morning.&lt;br /&gt;
* &#039;&#039;&#039;Duodenal ulcer:&#039;&#039;&#039; 20 mg once daily for 4 weeks, dose to be taken in the morning.&lt;br /&gt;
* &#039;&#039;&#039;Zollinger-Ellison syndrome:&#039;&#039;&#039; Initially 60 mg once daily, adjusted according to response, doses above 100 mg daily given in 2 divided doses; maximum 120 mg per day.&lt;br /&gt;
* &#039;&#039;&#039;H. pylori eradication:&#039;&#039;&#039; 20 mg twice daily.&lt;br /&gt;
&lt;br /&gt;
For renal dosing based on eGFR:&lt;br /&gt;
* No specific renal dose adjustment is typically required, but caution is advised in patients with severe renal impairment.&lt;br /&gt;
&lt;br /&gt;
== Side-Effects: Common and Serious Side Effects ==&lt;br /&gt;
Common side-effects may include:&lt;br /&gt;
* Constipation&lt;br /&gt;
* Cough&lt;br /&gt;
* Influenza like syndrome&lt;br /&gt;
&lt;br /&gt;
Serious side-effects may include:&lt;br /&gt;
* Increased Osteoporosis-related fractures, particularly in older adults&lt;br /&gt;
* Low blood magnesium levels&lt;br /&gt;
* &#039;&#039;Clostridium difficile&#039;&#039; infection in the colon&lt;br /&gt;
* Acute Tubulointerstitial Nephritis can manifest as decreased urine output or blood in the urine&lt;br /&gt;
* Vitamin B12 Deficiency: Symptoms include fatigue, sore tongue, and neurological issues&lt;br /&gt;
&lt;br /&gt;
==Pharmacokinetics==&lt;br /&gt;
 It undergoes hepatic metabolism and has a half-life of about 1 to 2 hours. The onset of action occurs within 1 hour, with a duration of action lasting up to 24 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Precautions ==&lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
The safety of rabeprazole during pregnancy is unclear; it should only be used if clearly needed.&lt;br /&gt;
&lt;br /&gt;
=== Breastfeeding ===&lt;br /&gt;
It is unknown whether rabeprazole passes into breast milk; caution is advised.&lt;br /&gt;
&lt;br /&gt;
=== Children and Elderly ===&lt;br /&gt;
Rabeprazole can be used in children aged 12 years and older for GERD treatment. Use in elderly patients may require careful monitoring due to potential increased sensitivity to side effects.&lt;br /&gt;
&lt;br /&gt;
=== Monitoring Items ===&lt;br /&gt;
Patients on rabeprazole should be monitored for:&lt;br /&gt;
* Signs of gastrointestinal bleeding&lt;br /&gt;
* Electrolyte levels, particularly magnesium&lt;br /&gt;
&lt;br /&gt;
=== Drug Interactions ===&lt;br /&gt;
Rabeprazole may interact with other medications, including:&lt;br /&gt;
* HIV Medications: Atazanavir, nelfinavir, and rilpivirine by reducing the absorption and effectiveness of these antiretroviral drugs, which may lead to treatment failure and resistance development.&lt;br /&gt;
* Clopidogrel: Rabeprazole may reduce the effectiveness of clopidogrel, a blood thinner, potentially increasing the risk of cardiovascular events.&lt;br /&gt;
* Itraconazole and ketoconazole: The absorption of these antifungal agents may be decreased when taken with rabeprazole due to altered gastric pH.&lt;br /&gt;
* Methotrexate: Concurrent use can lead to increased levels of methotrexate in the body, raising the risk of serious side effects such as kidney damage and anemia.&lt;br /&gt;
* Digoxin: Rabeprazole can increase the serum levels of digoxin, which is used to treat heart conditions, necessitating careful monitoring.&lt;br /&gt;
* St. John&#039;s Wort: This herbal supplement can reduce the effectiveness of rabeprazole by inducing hepatic enzymes that metabolize the drug.&lt;br /&gt;
&lt;br /&gt;
== FAQ ==&lt;br /&gt;
&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
Take rabeprazole orally, usually once daily before a meal. Swallow the tablet whole without crushing or chewing.&lt;br /&gt;
&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid concomitant use with certain medications like iron supplements and St. John&#039;s wort.&lt;br /&gt;
&lt;br /&gt;
=== What happens if I miss a dose? ===&lt;br /&gt;
If you miss a dose, take it as soon as you remember. If it&#039;s almost time for your next dose, skip the missed dose and resume your regular schedule. Do not double the dose.&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5030</id>
		<title>Rabeprazole</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5030"/>
		<updated>2025-01-05T14:42:45Z</updated>

		<summary type="html">&lt;p&gt;Annayung: /* Pharmacokinetics */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
= Rabeprazole =&lt;br /&gt;
==Pronunciation==&lt;br /&gt;
===Rabeprazole 20mg===&lt;br /&gt;
[[File:Rabeprazole 20mg.mp3]]&lt;br /&gt;
&lt;br /&gt;
== Drug Class ==&lt;br /&gt;
Rabeprazole belongs to the class of medications known as &#039;&#039;&#039;proton pump inhibitors (PPIs)&#039;&#039;&#039;. These drugs work by inhibiting gastric acid secretion.&lt;br /&gt;
&lt;br /&gt;
== Common Strengths ==&lt;br /&gt;
Rabeprazole is available in the following strengths:&lt;br /&gt;
* 10 mg delayed-release tablets&lt;br /&gt;
* 20 mg delayed-release tablets&lt;br /&gt;
&lt;br /&gt;
== Drug Trade Name ==&lt;br /&gt;
Rabeprazole is marketed under the trade name &#039;&#039;&#039;PARIET&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Drug Usage ==&lt;br /&gt;
Rabeprazole is primarily used for:&lt;br /&gt;
* Healing of erosive or ulcerative gastroesophageal reflux disease (GERD)&lt;br /&gt;
* Maintenance of healing of erosive or ulcerative GERD&lt;br /&gt;
* Treatment of symptomatic GERD&lt;br /&gt;
* Healing of duodenal ulcers&lt;br /&gt;
* Eradication of &#039;&#039;Helicobacter pylori&#039;&#039; to reduce the risk of duodenal ulcer recurrence&lt;br /&gt;
* Treatment of pathological hypersecretory conditions, including Zollinger-Ellison syndrome&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Rabeprazole works by selectively and irreversibly inhibiting the H^+, K^+-ATPase enzyme system (the proton pump) at the secretory surface of gastric parietal cells. This inhibition reduces gastric acid secretion, thereby alleviating symptoms associated with excess stomach acid.&lt;br /&gt;
&lt;br /&gt;
== Route of Administration ==&lt;br /&gt;
Rabeprazole is administered orally, available as delayed-release tablets.&lt;br /&gt;
&lt;br /&gt;
== Dosages for Normal People ==&lt;br /&gt;
The typical dosage for adults is:&lt;br /&gt;
* &#039;&#039;&#039;GERD treatment:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks; maintenance 10-20 mg daily.&lt;br /&gt;
* &#039;&#039;&#039;Benign gastric ulcer:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks, dose to be taken in the morning.&lt;br /&gt;
* &#039;&#039;&#039;Duodenal ulcer:&#039;&#039;&#039; 20 mg once daily for 4 weeks, dose to be taken in the morning.&lt;br /&gt;
* &#039;&#039;&#039;Zollinger-Ellison syndrome:&#039;&#039;&#039; Initially 60 mg once daily, adjusted according to response, doses above 100 mg daily given in 2 divided doses; maximum 120 mg per day.&lt;br /&gt;
* &#039;&#039;&#039;H. pylori eradication:&#039;&#039;&#039; 20 mg twice daily.&lt;br /&gt;
&lt;br /&gt;
For renal dosing based on eGFR:&lt;br /&gt;
* No specific renal dose adjustment is typically required, but caution is advised in patients with severe renal impairment.&lt;br /&gt;
&lt;br /&gt;
== Side-Effects: Common and Serious Side Effects ==&lt;br /&gt;
Common side-effects may include:&lt;br /&gt;
* Constipation&lt;br /&gt;
* Cough&lt;br /&gt;
* Influenza like syndrome&lt;br /&gt;
&lt;br /&gt;
Serious side-effects may include:&lt;br /&gt;
* Increased Osteoporosis-related fractures, particularly in older adults&lt;br /&gt;
* Low blood magnesium levels&lt;br /&gt;
* &#039;&#039;Clostridium difficile&#039;&#039; infection in the colon&lt;br /&gt;
* Acute Tubulointerstitial Nephritis can manifest as decreased urine output or blood in the urine&lt;br /&gt;
* Vitamin B12 Deficiency: Symptoms include fatigue, sore tongue, and neurological issues&lt;br /&gt;
&lt;br /&gt;
==Pharmacokinetics==&lt;br /&gt;
It undergoes hepatic metabolism and has a half-life of about 1 to 2 hours. The onset of action occurs within 1 hour, with a duration of action lasting up to 24 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Precautions ==&lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
The safety of rabeprazole during pregnancy is unclear; it should only be used if clearly needed.&lt;br /&gt;
&lt;br /&gt;
=== Breastfeeding ===&lt;br /&gt;
It is unknown whether rabeprazole passes into breast milk; caution is advised.&lt;br /&gt;
&lt;br /&gt;
=== Children and Elderly ===&lt;br /&gt;
Rabeprazole can be used in children aged 12 years and older for GERD treatment. Use in elderly patients may require careful monitoring due to potential increased sensitivity to side effects.&lt;br /&gt;
&lt;br /&gt;
=== Monitoring Items ===&lt;br /&gt;
Patients on rabeprazole should be monitored for:&lt;br /&gt;
* Signs of gastrointestinal bleeding&lt;br /&gt;
* Electrolyte levels, particularly magnesium&lt;br /&gt;
&lt;br /&gt;
=== Drug Interactions ===&lt;br /&gt;
Rabeprazole may interact with other medications, including:&lt;br /&gt;
* HIV Medications: Atazanavir, nelfinavir, and rilpivirine by reducing the absorption and effectiveness of these antiretroviral drugs, which may lead to treatment failure and resistance development.&lt;br /&gt;
* Clopidogrel: Rabeprazole may reduce the effectiveness of clopidogrel, a blood thinner, potentially increasing the risk of cardiovascular events.&lt;br /&gt;
* Itraconazole and ketoconazole: The absorption of these antifungal agents may be decreased when taken with rabeprazole due to altered gastric pH.&lt;br /&gt;
* Methotrexate: Concurrent use can lead to increased levels of methotrexate in the body, raising the risk of serious side effects such as kidney damage and anemia.&lt;br /&gt;
* Digoxin: Rabeprazole can increase the serum levels of digoxin, which is used to treat heart conditions, necessitating careful monitoring.&lt;br /&gt;
* St. John&#039;s Wort: This herbal supplement can reduce the effectiveness of rabeprazole by inducing hepatic enzymes that metabolize the drug.&lt;br /&gt;
&lt;br /&gt;
== FAQ ==&lt;br /&gt;
&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
Take rabeprazole orally, usually once daily before a meal. Swallow the tablet whole without crushing or chewing.&lt;br /&gt;
&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid concomitant use with certain medications like iron supplements and St. John&#039;s wort.&lt;br /&gt;
&lt;br /&gt;
=== What happens if I miss a dose? ===&lt;br /&gt;
If you miss a dose, take it as soon as you remember. If it&#039;s almost time for your next dose, skip the missed dose and resume your regular schedule. Do not double the dose.&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5029</id>
		<title>Rabeprazole</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5029"/>
		<updated>2025-01-05T14:41:54Z</updated>

		<summary type="html">&lt;p&gt;Annayung: /* Pharmacokinetics */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
= Rabeprazole =&lt;br /&gt;
==Pronunciation==&lt;br /&gt;
===Rabeprazole 20mg===&lt;br /&gt;
[[File:Rabeprazole 20mg.mp3]]&lt;br /&gt;
&lt;br /&gt;
== Drug Class ==&lt;br /&gt;
Rabeprazole belongs to the class of medications known as &#039;&#039;&#039;proton pump inhibitors (PPIs)&#039;&#039;&#039;. These drugs work by inhibiting gastric acid secretion.&lt;br /&gt;
&lt;br /&gt;
== Common Strengths ==&lt;br /&gt;
Rabeprazole is available in the following strengths:&lt;br /&gt;
* 10 mg delayed-release tablets&lt;br /&gt;
* 20 mg delayed-release tablets&lt;br /&gt;
&lt;br /&gt;
== Drug Trade Name ==&lt;br /&gt;
Rabeprazole is marketed under the trade name &#039;&#039;&#039;PARIET&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Drug Usage ==&lt;br /&gt;
Rabeprazole is primarily used for:&lt;br /&gt;
* Healing of erosive or ulcerative gastroesophageal reflux disease (GERD)&lt;br /&gt;
* Maintenance of healing of erosive or ulcerative GERD&lt;br /&gt;
* Treatment of symptomatic GERD&lt;br /&gt;
* Healing of duodenal ulcers&lt;br /&gt;
* Eradication of &#039;&#039;Helicobacter pylori&#039;&#039; to reduce the risk of duodenal ulcer recurrence&lt;br /&gt;
* Treatment of pathological hypersecretory conditions, including Zollinger-Ellison syndrome&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Rabeprazole works by selectively and irreversibly inhibiting the H^+, K^+-ATPase enzyme system (the proton pump) at the secretory surface of gastric parietal cells. This inhibition reduces gastric acid secretion, thereby alleviating symptoms associated with excess stomach acid.&lt;br /&gt;
&lt;br /&gt;
== Route of Administration ==&lt;br /&gt;
Rabeprazole is administered orally, available as delayed-release tablets.&lt;br /&gt;
&lt;br /&gt;
== Dosages for Normal People ==&lt;br /&gt;
The typical dosage for adults is:&lt;br /&gt;
* &#039;&#039;&#039;GERD treatment:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks; maintenance 10-20 mg daily.&lt;br /&gt;
* &#039;&#039;&#039;Benign gastric ulcer:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks, dose to be taken in the morning.&lt;br /&gt;
* &#039;&#039;&#039;Duodenal ulcer:&#039;&#039;&#039; 20 mg once daily for 4 weeks, dose to be taken in the morning.&lt;br /&gt;
* &#039;&#039;&#039;Zollinger-Ellison syndrome:&#039;&#039;&#039; Initially 60 mg once daily, adjusted according to response, doses above 100 mg daily given in 2 divided doses; maximum 120 mg per day.&lt;br /&gt;
* &#039;&#039;&#039;H. pylori eradication:&#039;&#039;&#039; 20 mg twice daily.&lt;br /&gt;
&lt;br /&gt;
For renal dosing based on eGFR:&lt;br /&gt;
* No specific renal dose adjustment is typically required, but caution is advised in patients with severe renal impairment.&lt;br /&gt;
&lt;br /&gt;
== Side-Effects: Common and Serious Side Effects ==&lt;br /&gt;
Common side-effects may include:&lt;br /&gt;
* Constipation&lt;br /&gt;
* Cough&lt;br /&gt;
* Influenza like syndrome&lt;br /&gt;
&lt;br /&gt;
Serious side-effects may include:&lt;br /&gt;
* Increased Osteoporosis-related fractures, particularly in older adults&lt;br /&gt;
* Low blood magnesium levels&lt;br /&gt;
* &#039;&#039;Clostridium difficile&#039;&#039; infection in the colon&lt;br /&gt;
* Acute Tubulointerstitial Nephritis can manifest as decreased urine output or blood in the urine&lt;br /&gt;
* Vitamin B12 Deficiency: Symptoms include fatigue, sore tongue, and neurological issues&lt;br /&gt;
&lt;br /&gt;
==Pharmacokinetics==&lt;br /&gt;
 It undergoes hepatic metabolism and has a half-life of about 1 to 2 hours. The onset of action occurs within 1 hour, with a duration of action lasting up to 24 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Precautions ==&lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
The safety of rabeprazole during pregnancy is unclear; it should only be used if clearly needed.&lt;br /&gt;
&lt;br /&gt;
=== Breastfeeding ===&lt;br /&gt;
It is unknown whether rabeprazole passes into breast milk; caution is advised.&lt;br /&gt;
&lt;br /&gt;
=== Children and Elderly ===&lt;br /&gt;
Rabeprazole can be used in children aged 12 years and older for GERD treatment. Use in elderly patients may require careful monitoring due to potential increased sensitivity to side effects.&lt;br /&gt;
&lt;br /&gt;
=== Monitoring Items ===&lt;br /&gt;
Patients on rabeprazole should be monitored for:&lt;br /&gt;
* Signs of gastrointestinal bleeding&lt;br /&gt;
* Electrolyte levels, particularly magnesium&lt;br /&gt;
&lt;br /&gt;
=== Drug Interactions ===&lt;br /&gt;
Rabeprazole may interact with other medications, including:&lt;br /&gt;
* HIV Medications: Atazanavir, nelfinavir, and rilpivirine by reducing the absorption and effectiveness of these antiretroviral drugs, which may lead to treatment failure and resistance development.&lt;br /&gt;
* Clopidogrel: Rabeprazole may reduce the effectiveness of clopidogrel, a blood thinner, potentially increasing the risk of cardiovascular events.&lt;br /&gt;
* Itraconazole and ketoconazole: The absorption of these antifungal agents may be decreased when taken with rabeprazole due to altered gastric pH.&lt;br /&gt;
* Methotrexate: Concurrent use can lead to increased levels of methotrexate in the body, raising the risk of serious side effects such as kidney damage and anemia.&lt;br /&gt;
* Digoxin: Rabeprazole can increase the serum levels of digoxin, which is used to treat heart conditions, necessitating careful monitoring.&lt;br /&gt;
* St. John&#039;s Wort: This herbal supplement can reduce the effectiveness of rabeprazole by inducing hepatic enzymes that metabolize the drug.&lt;br /&gt;
&lt;br /&gt;
== FAQ ==&lt;br /&gt;
&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
Take rabeprazole orally, usually once daily before a meal. Swallow the tablet whole without crushing or chewing.&lt;br /&gt;
&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid concomitant use with certain medications like iron supplements and St. John&#039;s wort.&lt;br /&gt;
&lt;br /&gt;
=== What happens if I miss a dose? ===&lt;br /&gt;
If you miss a dose, take it as soon as you remember. If it&#039;s almost time for your next dose, skip the missed dose and resume your regular schedule. Do not double the dose.&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5028</id>
		<title>Rabeprazole</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5028"/>
		<updated>2025-01-05T14:39:28Z</updated>

		<summary type="html">&lt;p&gt;Annayung: /* Pharmacokinetics */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
= Rabeprazole =&lt;br /&gt;
==Pronunciation==&lt;br /&gt;
===Rabeprazole 20mg===&lt;br /&gt;
[[File:Rabeprazole 20mg.mp3]]&lt;br /&gt;
&lt;br /&gt;
== Drug Class ==&lt;br /&gt;
Rabeprazole belongs to the class of medications known as &#039;&#039;&#039;proton pump inhibitors (PPIs)&#039;&#039;&#039;. These drugs work by inhibiting gastric acid secretion.&lt;br /&gt;
&lt;br /&gt;
== Common Strengths ==&lt;br /&gt;
Rabeprazole is available in the following strengths:&lt;br /&gt;
* 10 mg delayed-release tablets&lt;br /&gt;
* 20 mg delayed-release tablets&lt;br /&gt;
&lt;br /&gt;
== Drug Trade Name ==&lt;br /&gt;
Rabeprazole is marketed under the trade name &#039;&#039;&#039;PARIET&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Drug Usage ==&lt;br /&gt;
Rabeprazole is primarily used for:&lt;br /&gt;
* Healing of erosive or ulcerative gastroesophageal reflux disease (GERD)&lt;br /&gt;
* Maintenance of healing of erosive or ulcerative GERD&lt;br /&gt;
* Treatment of symptomatic GERD&lt;br /&gt;
* Healing of duodenal ulcers&lt;br /&gt;
* Eradication of &#039;&#039;Helicobacter pylori&#039;&#039; to reduce the risk of duodenal ulcer recurrence&lt;br /&gt;
* Treatment of pathological hypersecretory conditions, including Zollinger-Ellison syndrome&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Rabeprazole works by selectively and irreversibly inhibiting the H^+, K^+-ATPase enzyme system (the proton pump) at the secretory surface of gastric parietal cells. This inhibition reduces gastric acid secretion, thereby alleviating symptoms associated with excess stomach acid.&lt;br /&gt;
&lt;br /&gt;
== Route of Administration ==&lt;br /&gt;
Rabeprazole is administered orally, available as delayed-release tablets.&lt;br /&gt;
&lt;br /&gt;
== Dosages for Normal People ==&lt;br /&gt;
The typical dosage for adults is:&lt;br /&gt;
* &#039;&#039;&#039;GERD treatment:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks; maintenance 10-20 mg daily.&lt;br /&gt;
* &#039;&#039;&#039;Benign gastric ulcer:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks, dose to be taken in the morning.&lt;br /&gt;
* &#039;&#039;&#039;Duodenal ulcer:&#039;&#039;&#039; 20 mg once daily for 4 weeks, dose to be taken in the morning.&lt;br /&gt;
* &#039;&#039;&#039;Zollinger-Ellison syndrome:&#039;&#039;&#039; Initially 60 mg once daily, adjusted according to response, doses above 100 mg daily given in 2 divided doses; maximum 120 mg per day.&lt;br /&gt;
* &#039;&#039;&#039;H. pylori eradication:&#039;&#039;&#039; 20 mg twice daily.&lt;br /&gt;
&lt;br /&gt;
For renal dosing based on eGFR:&lt;br /&gt;
* No specific renal dose adjustment is typically required, but caution is advised in patients with severe renal impairment.&lt;br /&gt;
&lt;br /&gt;
== Side-Effects: Common and Serious Side Effects ==&lt;br /&gt;
Common side-effects may include:&lt;br /&gt;
* Constipation&lt;br /&gt;
* Cough&lt;br /&gt;
* Influenza like syndrome&lt;br /&gt;
&lt;br /&gt;
Serious side-effects may include:&lt;br /&gt;
* Increased Osteoporosis-related fractures, particularly in older adults&lt;br /&gt;
* Low blood magnesium levels&lt;br /&gt;
* &#039;&#039;Clostridium difficile&#039;&#039; infection in the colon&lt;br /&gt;
* Acute Tubulointerstitial Nephritis can manifest as decreased urine output or blood in the urine&lt;br /&gt;
* Vitamin B12 Deficiency: Symptoms include fatigue, sore tongue, and neurological issues&lt;br /&gt;
&lt;br /&gt;
=== Pharmacokinetics ===&lt;br /&gt;
 It undergoes hepatic metabolism and has a half-life of about 1 to 2 hours. The onset of action occurs within 1 hour, with a duration of action lasting up to 24 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Precautions ==&lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
The safety of rabeprazole during pregnancy is unclear; it should only be used if clearly needed.&lt;br /&gt;
&lt;br /&gt;
=== Breastfeeding ===&lt;br /&gt;
It is unknown whether rabeprazole passes into breast milk; caution is advised.&lt;br /&gt;
&lt;br /&gt;
=== Children and Elderly ===&lt;br /&gt;
Rabeprazole can be used in children aged 12 years and older for GERD treatment. Use in elderly patients may require careful monitoring due to potential increased sensitivity to side effects.&lt;br /&gt;
&lt;br /&gt;
=== Monitoring Items ===&lt;br /&gt;
Patients on rabeprazole should be monitored for:&lt;br /&gt;
* Signs of gastrointestinal bleeding&lt;br /&gt;
* Electrolyte levels, particularly magnesium&lt;br /&gt;
&lt;br /&gt;
=== Drug Interactions ===&lt;br /&gt;
Rabeprazole may interact with other medications, including:&lt;br /&gt;
* HIV Medications: Atazanavir, nelfinavir, and rilpivirine by reducing the absorption and effectiveness of these antiretroviral drugs, which may lead to treatment failure and resistance development.&lt;br /&gt;
* Clopidogrel: Rabeprazole may reduce the effectiveness of clopidogrel, a blood thinner, potentially increasing the risk of cardiovascular events.&lt;br /&gt;
* Itraconazole and ketoconazole: The absorption of these antifungal agents may be decreased when taken with rabeprazole due to altered gastric pH.&lt;br /&gt;
* Methotrexate: Concurrent use can lead to increased levels of methotrexate in the body, raising the risk of serious side effects such as kidney damage and anemia.&lt;br /&gt;
* Digoxin: Rabeprazole can increase the serum levels of digoxin, which is used to treat heart conditions, necessitating careful monitoring.&lt;br /&gt;
* St. John&#039;s Wort: This herbal supplement can reduce the effectiveness of rabeprazole by inducing hepatic enzymes that metabolize the drug.&lt;br /&gt;
&lt;br /&gt;
== FAQ ==&lt;br /&gt;
&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
Take rabeprazole orally, usually once daily before a meal. Swallow the tablet whole without crushing or chewing.&lt;br /&gt;
&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid concomitant use with certain medications like iron supplements and St. John&#039;s wort.&lt;br /&gt;
&lt;br /&gt;
=== What happens if I miss a dose? ===&lt;br /&gt;
If you miss a dose, take it as soon as you remember. If it&#039;s almost time for your next dose, skip the missed dose and resume your regular schedule. Do not double the dose.&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5027</id>
		<title>Rabeprazole</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5027"/>
		<updated>2025-01-05T14:38:54Z</updated>

		<summary type="html">&lt;p&gt;Annayung: /* What should I avoid while taking? */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
= Rabeprazole =&lt;br /&gt;
==Pronunciation==&lt;br /&gt;
===Rabeprazole 20mg===&lt;br /&gt;
[[File:Rabeprazole 20mg.mp3]]&lt;br /&gt;
&lt;br /&gt;
== Drug Class ==&lt;br /&gt;
Rabeprazole belongs to the class of medications known as &#039;&#039;&#039;proton pump inhibitors (PPIs)&#039;&#039;&#039;. These drugs work by inhibiting gastric acid secretion.&lt;br /&gt;
&lt;br /&gt;
== Common Strengths ==&lt;br /&gt;
Rabeprazole is available in the following strengths:&lt;br /&gt;
* 10 mg delayed-release tablets&lt;br /&gt;
* 20 mg delayed-release tablets&lt;br /&gt;
&lt;br /&gt;
== Drug Trade Name ==&lt;br /&gt;
Rabeprazole is marketed under the trade name &#039;&#039;&#039;PARIET&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Drug Usage ==&lt;br /&gt;
Rabeprazole is primarily used for:&lt;br /&gt;
* Healing of erosive or ulcerative gastroesophageal reflux disease (GERD)&lt;br /&gt;
* Maintenance of healing of erosive or ulcerative GERD&lt;br /&gt;
* Treatment of symptomatic GERD&lt;br /&gt;
* Healing of duodenal ulcers&lt;br /&gt;
* Eradication of &#039;&#039;Helicobacter pylori&#039;&#039; to reduce the risk of duodenal ulcer recurrence&lt;br /&gt;
* Treatment of pathological hypersecretory conditions, including Zollinger-Ellison syndrome&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Rabeprazole works by selectively and irreversibly inhibiting the H^+, K^+-ATPase enzyme system (the proton pump) at the secretory surface of gastric parietal cells. This inhibition reduces gastric acid secretion, thereby alleviating symptoms associated with excess stomach acid.&lt;br /&gt;
&lt;br /&gt;
== Route of Administration ==&lt;br /&gt;
Rabeprazole is administered orally, available as delayed-release tablets.&lt;br /&gt;
&lt;br /&gt;
== Dosages for Normal People ==&lt;br /&gt;
The typical dosage for adults is:&lt;br /&gt;
* &#039;&#039;&#039;GERD treatment:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks; maintenance 10-20 mg daily.&lt;br /&gt;
* &#039;&#039;&#039;Benign gastric ulcer:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks, dose to be taken in the morning.&lt;br /&gt;
* &#039;&#039;&#039;Duodenal ulcer:&#039;&#039;&#039; 20 mg once daily for 4 weeks, dose to be taken in the morning.&lt;br /&gt;
* &#039;&#039;&#039;Zollinger-Ellison syndrome:&#039;&#039;&#039; Initially 60 mg once daily, adjusted according to response, doses above 100 mg daily given in 2 divided doses; maximum 120 mg per day.&lt;br /&gt;
* &#039;&#039;&#039;H. pylori eradication:&#039;&#039;&#039; 20 mg twice daily.&lt;br /&gt;
&lt;br /&gt;
For renal dosing based on eGFR:&lt;br /&gt;
* No specific renal dose adjustment is typically required, but caution is advised in patients with severe renal impairment.&lt;br /&gt;
&lt;br /&gt;
== Side-Effects: Common and Serious Side Effects ==&lt;br /&gt;
Common side-effects may include:&lt;br /&gt;
* Constipation&lt;br /&gt;
* Cough&lt;br /&gt;
* Influenza like syndrome&lt;br /&gt;
&lt;br /&gt;
Serious side-effects may include:&lt;br /&gt;
* Increased Osteoporosis-related fractures, particularly in older adults&lt;br /&gt;
* Low blood magnesium levels&lt;br /&gt;
* &#039;&#039;Clostridium difficile&#039;&#039; infection in the colon&lt;br /&gt;
* Acute Tubulointerstitial Nephritis can manifest as decreased urine output or blood in the urine&lt;br /&gt;
* Vitamin B12 Deficiency: Symptoms include fatigue, sore tongue, and neurological issues&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
 It undergoes hepatic metabolism and has a half-life of about 1 to 2 hours. The onset of action occurs within 1 hour, with a duration of action lasting up to 24 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Precautions ==&lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
The safety of rabeprazole during pregnancy is unclear; it should only be used if clearly needed.&lt;br /&gt;
&lt;br /&gt;
=== Breastfeeding ===&lt;br /&gt;
It is unknown whether rabeprazole passes into breast milk; caution is advised.&lt;br /&gt;
&lt;br /&gt;
=== Children and Elderly ===&lt;br /&gt;
Rabeprazole can be used in children aged 12 years and older for GERD treatment. Use in elderly patients may require careful monitoring due to potential increased sensitivity to side effects.&lt;br /&gt;
&lt;br /&gt;
=== Monitoring Items ===&lt;br /&gt;
Patients on rabeprazole should be monitored for:&lt;br /&gt;
* Signs of gastrointestinal bleeding&lt;br /&gt;
* Electrolyte levels, particularly magnesium&lt;br /&gt;
&lt;br /&gt;
=== Drug Interactions ===&lt;br /&gt;
Rabeprazole may interact with other medications, including:&lt;br /&gt;
* HIV Medications: Atazanavir, nelfinavir, and rilpivirine by reducing the absorption and effectiveness of these antiretroviral drugs, which may lead to treatment failure and resistance development.&lt;br /&gt;
* Clopidogrel: Rabeprazole may reduce the effectiveness of clopidogrel, a blood thinner, potentially increasing the risk of cardiovascular events.&lt;br /&gt;
* Itraconazole and ketoconazole: The absorption of these antifungal agents may be decreased when taken with rabeprazole due to altered gastric pH.&lt;br /&gt;
* Methotrexate: Concurrent use can lead to increased levels of methotrexate in the body, raising the risk of serious side effects such as kidney damage and anemia.&lt;br /&gt;
* Digoxin: Rabeprazole can increase the serum levels of digoxin, which is used to treat heart conditions, necessitating careful monitoring.&lt;br /&gt;
* St. John&#039;s Wort: This herbal supplement can reduce the effectiveness of rabeprazole by inducing hepatic enzymes that metabolize the drug.&lt;br /&gt;
&lt;br /&gt;
== FAQ ==&lt;br /&gt;
&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
Take rabeprazole orally, usually once daily before a meal. Swallow the tablet whole without crushing or chewing.&lt;br /&gt;
&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid concomitant use with certain medications like iron supplements and St. John&#039;s wort.&lt;br /&gt;
&lt;br /&gt;
=== What happens if I miss a dose? ===&lt;br /&gt;
If you miss a dose, take it as soon as you remember. If it&#039;s almost time for your next dose, skip the missed dose and resume your regular schedule. Do not double the dose.&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5026</id>
		<title>Rabeprazole</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5026"/>
		<updated>2025-01-05T14:37:00Z</updated>

		<summary type="html">&lt;p&gt;Annayung: /* Drug Interactions */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
= Rabeprazole =&lt;br /&gt;
==Pronunciation==&lt;br /&gt;
===Rabeprazole 20mg===&lt;br /&gt;
[[File:Rabeprazole 20mg.mp3]]&lt;br /&gt;
&lt;br /&gt;
== Drug Class ==&lt;br /&gt;
Rabeprazole belongs to the class of medications known as &#039;&#039;&#039;proton pump inhibitors (PPIs)&#039;&#039;&#039;. These drugs work by inhibiting gastric acid secretion.&lt;br /&gt;
&lt;br /&gt;
== Common Strengths ==&lt;br /&gt;
Rabeprazole is available in the following strengths:&lt;br /&gt;
* 10 mg delayed-release tablets&lt;br /&gt;
* 20 mg delayed-release tablets&lt;br /&gt;
&lt;br /&gt;
== Drug Trade Name ==&lt;br /&gt;
Rabeprazole is marketed under the trade name &#039;&#039;&#039;PARIET&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Drug Usage ==&lt;br /&gt;
Rabeprazole is primarily used for:&lt;br /&gt;
* Healing of erosive or ulcerative gastroesophageal reflux disease (GERD)&lt;br /&gt;
* Maintenance of healing of erosive or ulcerative GERD&lt;br /&gt;
* Treatment of symptomatic GERD&lt;br /&gt;
* Healing of duodenal ulcers&lt;br /&gt;
* Eradication of &#039;&#039;Helicobacter pylori&#039;&#039; to reduce the risk of duodenal ulcer recurrence&lt;br /&gt;
* Treatment of pathological hypersecretory conditions, including Zollinger-Ellison syndrome&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Rabeprazole works by selectively and irreversibly inhibiting the H^+, K^+-ATPase enzyme system (the proton pump) at the secretory surface of gastric parietal cells. This inhibition reduces gastric acid secretion, thereby alleviating symptoms associated with excess stomach acid.&lt;br /&gt;
&lt;br /&gt;
== Route of Administration ==&lt;br /&gt;
Rabeprazole is administered orally, available as delayed-release tablets.&lt;br /&gt;
&lt;br /&gt;
== Dosages for Normal People ==&lt;br /&gt;
The typical dosage for adults is:&lt;br /&gt;
* &#039;&#039;&#039;GERD treatment:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks; maintenance 10-20 mg daily.&lt;br /&gt;
* &#039;&#039;&#039;Benign gastric ulcer:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks, dose to be taken in the morning.&lt;br /&gt;
* &#039;&#039;&#039;Duodenal ulcer:&#039;&#039;&#039; 20 mg once daily for 4 weeks, dose to be taken in the morning.&lt;br /&gt;
* &#039;&#039;&#039;Zollinger-Ellison syndrome:&#039;&#039;&#039; Initially 60 mg once daily, adjusted according to response, doses above 100 mg daily given in 2 divided doses; maximum 120 mg per day.&lt;br /&gt;
* &#039;&#039;&#039;H. pylori eradication:&#039;&#039;&#039; 20 mg twice daily.&lt;br /&gt;
&lt;br /&gt;
For renal dosing based on eGFR:&lt;br /&gt;
* No specific renal dose adjustment is typically required, but caution is advised in patients with severe renal impairment.&lt;br /&gt;
&lt;br /&gt;
== Side-Effects: Common and Serious Side Effects ==&lt;br /&gt;
Common side-effects may include:&lt;br /&gt;
* Constipation&lt;br /&gt;
* Cough&lt;br /&gt;
* Influenza like syndrome&lt;br /&gt;
&lt;br /&gt;
Serious side-effects may include:&lt;br /&gt;
* Increased Osteoporosis-related fractures, particularly in older adults&lt;br /&gt;
* Low blood magnesium levels&lt;br /&gt;
* &#039;&#039;Clostridium difficile&#039;&#039; infection in the colon&lt;br /&gt;
* Acute Tubulointerstitial Nephritis can manifest as decreased urine output or blood in the urine&lt;br /&gt;
* Vitamin B12 Deficiency: Symptoms include fatigue, sore tongue, and neurological issues&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
 It undergoes hepatic metabolism and has a half-life of about 1 to 2 hours. The onset of action occurs within 1 hour, with a duration of action lasting up to 24 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Precautions ==&lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
The safety of rabeprazole during pregnancy is unclear; it should only be used if clearly needed.&lt;br /&gt;
&lt;br /&gt;
=== Breastfeeding ===&lt;br /&gt;
It is unknown whether rabeprazole passes into breast milk; caution is advised.&lt;br /&gt;
&lt;br /&gt;
=== Children and Elderly ===&lt;br /&gt;
Rabeprazole can be used in children aged 12 years and older for GERD treatment. Use in elderly patients may require careful monitoring due to potential increased sensitivity to side effects.&lt;br /&gt;
&lt;br /&gt;
=== Monitoring Items ===&lt;br /&gt;
Patients on rabeprazole should be monitored for:&lt;br /&gt;
* Signs of gastrointestinal bleeding&lt;br /&gt;
* Electrolyte levels, particularly magnesium&lt;br /&gt;
&lt;br /&gt;
=== Drug Interactions ===&lt;br /&gt;
Rabeprazole may interact with other medications, including:&lt;br /&gt;
* HIV Medications: Atazanavir, nelfinavir, and rilpivirine by reducing the absorption and effectiveness of these antiretroviral drugs, which may lead to treatment failure and resistance development.&lt;br /&gt;
* Clopidogrel: Rabeprazole may reduce the effectiveness of clopidogrel, a blood thinner, potentially increasing the risk of cardiovascular events.&lt;br /&gt;
* Itraconazole and ketoconazole: The absorption of these antifungal agents may be decreased when taken with rabeprazole due to altered gastric pH.&lt;br /&gt;
* Methotrexate: Concurrent use can lead to increased levels of methotrexate in the body, raising the risk of serious side effects such as kidney damage and anemia.&lt;br /&gt;
* Digoxin: Rabeprazole can increase the serum levels of digoxin, which is used to treat heart conditions, necessitating careful monitoring.&lt;br /&gt;
* St. John&#039;s Wort: This herbal supplement can reduce the effectiveness of rabeprazole by inducing hepatic enzymes that metabolize the drug.&lt;br /&gt;
&lt;br /&gt;
== FAQ ==&lt;br /&gt;
&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
Take rabeprazole orally, usually once daily before a meal. Swallow the tablet whole without crushing or chewing.&lt;br /&gt;
&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid alcohol and NSAIDs unless directed by a healthcare provider, as they may increase the risk of gastrointestinal side effects.&lt;br /&gt;
&lt;br /&gt;
=== What happens if I miss a dose? ===&lt;br /&gt;
If you miss a dose, take it as soon as you remember. If it&#039;s almost time for your next dose, skip the missed dose and resume your regular schedule. Do not double the dose.&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5025</id>
		<title>Rabeprazole</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5025"/>
		<updated>2025-01-05T14:28:22Z</updated>

		<summary type="html">&lt;p&gt;Annayung: /* Pharmacokinetics */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
= Rabeprazole =&lt;br /&gt;
==Pronunciation==&lt;br /&gt;
===Rabeprazole 20mg===&lt;br /&gt;
[[File:Rabeprazole 20mg.mp3]]&lt;br /&gt;
&lt;br /&gt;
== Drug Class ==&lt;br /&gt;
Rabeprazole belongs to the class of medications known as &#039;&#039;&#039;proton pump inhibitors (PPIs)&#039;&#039;&#039;. These drugs work by inhibiting gastric acid secretion.&lt;br /&gt;
&lt;br /&gt;
== Common Strengths ==&lt;br /&gt;
Rabeprazole is available in the following strengths:&lt;br /&gt;
* 10 mg delayed-release tablets&lt;br /&gt;
* 20 mg delayed-release tablets&lt;br /&gt;
&lt;br /&gt;
== Drug Trade Name ==&lt;br /&gt;
Rabeprazole is marketed under the trade name &#039;&#039;&#039;PARIET&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Drug Usage ==&lt;br /&gt;
Rabeprazole is primarily used for:&lt;br /&gt;
* Healing of erosive or ulcerative gastroesophageal reflux disease (GERD)&lt;br /&gt;
* Maintenance of healing of erosive or ulcerative GERD&lt;br /&gt;
* Treatment of symptomatic GERD&lt;br /&gt;
* Healing of duodenal ulcers&lt;br /&gt;
* Eradication of &#039;&#039;Helicobacter pylori&#039;&#039; to reduce the risk of duodenal ulcer recurrence&lt;br /&gt;
* Treatment of pathological hypersecretory conditions, including Zollinger-Ellison syndrome&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Rabeprazole works by selectively and irreversibly inhibiting the H^+, K^+-ATPase enzyme system (the proton pump) at the secretory surface of gastric parietal cells. This inhibition reduces gastric acid secretion, thereby alleviating symptoms associated with excess stomach acid.&lt;br /&gt;
&lt;br /&gt;
== Route of Administration ==&lt;br /&gt;
Rabeprazole is administered orally, available as delayed-release tablets.&lt;br /&gt;
&lt;br /&gt;
== Dosages for Normal People ==&lt;br /&gt;
The typical dosage for adults is:&lt;br /&gt;
* &#039;&#039;&#039;GERD treatment:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks; maintenance 10-20 mg daily.&lt;br /&gt;
* &#039;&#039;&#039;Benign gastric ulcer:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks, dose to be taken in the morning.&lt;br /&gt;
* &#039;&#039;&#039;Duodenal ulcer:&#039;&#039;&#039; 20 mg once daily for 4 weeks, dose to be taken in the morning.&lt;br /&gt;
* &#039;&#039;&#039;Zollinger-Ellison syndrome:&#039;&#039;&#039; Initially 60 mg once daily, adjusted according to response, doses above 100 mg daily given in 2 divided doses; maximum 120 mg per day.&lt;br /&gt;
* &#039;&#039;&#039;H. pylori eradication:&#039;&#039;&#039; 20 mg twice daily.&lt;br /&gt;
&lt;br /&gt;
For renal dosing based on eGFR:&lt;br /&gt;
* No specific renal dose adjustment is typically required, but caution is advised in patients with severe renal impairment.&lt;br /&gt;
&lt;br /&gt;
== Side-Effects: Common and Serious Side Effects ==&lt;br /&gt;
Common side-effects may include:&lt;br /&gt;
* Constipation&lt;br /&gt;
* Cough&lt;br /&gt;
* Influenza like syndrome&lt;br /&gt;
&lt;br /&gt;
Serious side-effects may include:&lt;br /&gt;
* Increased Osteoporosis-related fractures, particularly in older adults&lt;br /&gt;
* Low blood magnesium levels&lt;br /&gt;
* &#039;&#039;Clostridium difficile&#039;&#039; infection in the colon&lt;br /&gt;
* Acute Tubulointerstitial Nephritis can manifest as decreased urine output or blood in the urine&lt;br /&gt;
* Vitamin B12 Deficiency: Symptoms include fatigue, sore tongue, and neurological issues&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
 It undergoes hepatic metabolism and has a half-life of about 1 to 2 hours. The onset of action occurs within 1 hour, with a duration of action lasting up to 24 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Precautions ==&lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
The safety of rabeprazole during pregnancy is unclear; it should only be used if clearly needed.&lt;br /&gt;
&lt;br /&gt;
=== Breastfeeding ===&lt;br /&gt;
It is unknown whether rabeprazole passes into breast milk; caution is advised.&lt;br /&gt;
&lt;br /&gt;
=== Children and Elderly ===&lt;br /&gt;
Rabeprazole can be used in children aged 12 years and older for GERD treatment. Use in elderly patients may require careful monitoring due to potential increased sensitivity to side effects.&lt;br /&gt;
&lt;br /&gt;
=== Monitoring Items ===&lt;br /&gt;
Patients on rabeprazole should be monitored for:&lt;br /&gt;
* Signs of gastrointestinal bleeding&lt;br /&gt;
* Electrolyte levels, particularly magnesium&lt;br /&gt;
&lt;br /&gt;
=== Drug Interactions ===&lt;br /&gt;
Rabeprazole may interact with other medications, including certain anticoagulants, antifungals, and antiretrovirals. It is important to inform healthcare providers about all medications being taken.&lt;br /&gt;
&lt;br /&gt;
== FAQ ==&lt;br /&gt;
&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
Take rabeprazole orally, usually once daily before a meal. Swallow the tablet whole without crushing or chewing.&lt;br /&gt;
&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid alcohol and NSAIDs unless directed by a healthcare provider, as they may increase the risk of gastrointestinal side effects.&lt;br /&gt;
&lt;br /&gt;
=== What happens if I miss a dose? ===&lt;br /&gt;
If you miss a dose, take it as soon as you remember. If it&#039;s almost time for your next dose, skip the missed dose and resume your regular schedule. Do not double the dose.&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5024</id>
		<title>Rabeprazole</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5024"/>
		<updated>2025-01-05T14:27:33Z</updated>

		<summary type="html">&lt;p&gt;Annayung: /* Side Effects: Common and Serious Side Effects */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
= Rabeprazole =&lt;br /&gt;
==Pronunciation==&lt;br /&gt;
===Rabeprazole 20mg===&lt;br /&gt;
[[File:Rabeprazole 20mg.mp3]]&lt;br /&gt;
&lt;br /&gt;
== Drug Class ==&lt;br /&gt;
Rabeprazole belongs to the class of medications known as &#039;&#039;&#039;proton pump inhibitors (PPIs)&#039;&#039;&#039;. These drugs work by inhibiting gastric acid secretion.&lt;br /&gt;
&lt;br /&gt;
== Common Strengths ==&lt;br /&gt;
Rabeprazole is available in the following strengths:&lt;br /&gt;
* 10 mg delayed-release tablets&lt;br /&gt;
* 20 mg delayed-release tablets&lt;br /&gt;
&lt;br /&gt;
== Drug Trade Name ==&lt;br /&gt;
Rabeprazole is marketed under the trade name &#039;&#039;&#039;PARIET&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Drug Usage ==&lt;br /&gt;
Rabeprazole is primarily used for:&lt;br /&gt;
* Healing of erosive or ulcerative gastroesophageal reflux disease (GERD)&lt;br /&gt;
* Maintenance of healing of erosive or ulcerative GERD&lt;br /&gt;
* Treatment of symptomatic GERD&lt;br /&gt;
* Healing of duodenal ulcers&lt;br /&gt;
* Eradication of &#039;&#039;Helicobacter pylori&#039;&#039; to reduce the risk of duodenal ulcer recurrence&lt;br /&gt;
* Treatment of pathological hypersecretory conditions, including Zollinger-Ellison syndrome&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Rabeprazole works by selectively and irreversibly inhibiting the H^+, K^+-ATPase enzyme system (the proton pump) at the secretory surface of gastric parietal cells. This inhibition reduces gastric acid secretion, thereby alleviating symptoms associated with excess stomach acid.&lt;br /&gt;
&lt;br /&gt;
== Route of Administration ==&lt;br /&gt;
Rabeprazole is administered orally, available as delayed-release tablets.&lt;br /&gt;
&lt;br /&gt;
== Dosages for Normal People ==&lt;br /&gt;
The typical dosage for adults is:&lt;br /&gt;
* &#039;&#039;&#039;GERD treatment:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks; maintenance 10-20 mg daily.&lt;br /&gt;
* &#039;&#039;&#039;Benign gastric ulcer:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks, dose to be taken in the morning.&lt;br /&gt;
* &#039;&#039;&#039;Duodenal ulcer:&#039;&#039;&#039; 20 mg once daily for 4 weeks, dose to be taken in the morning.&lt;br /&gt;
* &#039;&#039;&#039;Zollinger-Ellison syndrome:&#039;&#039;&#039; Initially 60 mg once daily, adjusted according to response, doses above 100 mg daily given in 2 divided doses; maximum 120 mg per day.&lt;br /&gt;
* &#039;&#039;&#039;H. pylori eradication:&#039;&#039;&#039; 20 mg twice daily.&lt;br /&gt;
&lt;br /&gt;
For renal dosing based on eGFR:&lt;br /&gt;
* No specific renal dose adjustment is typically required, but caution is advised in patients with severe renal impairment.&lt;br /&gt;
&lt;br /&gt;
== Side-Effects: Common and Serious Side Effects ==&lt;br /&gt;
Common side-effects may include:&lt;br /&gt;
* Constipation&lt;br /&gt;
* Cough&lt;br /&gt;
* Influenza like syndrome&lt;br /&gt;
&lt;br /&gt;
Serious side-effects may include:&lt;br /&gt;
* Increased Osteoporosis-related fractures, particularly in older adults&lt;br /&gt;
* Low blood magnesium levels&lt;br /&gt;
* &#039;&#039;Clostridium difficile&#039;&#039; infection in the colon&lt;br /&gt;
* Acute Tubulointerstitial Nephritis can manifest as decreased urine output or blood in the urine&lt;br /&gt;
* Vitamin B12 Deficiency: Symptoms include fatigue, sore tongue, and neurological issues&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
Rabeprazole has an absolute bioavailability of approximately 52%. It undergoes hepatic metabolism and has a half-life of about 1 to 2 hours. The onset of action occurs within 1 hour, with a duration of action lasting up to 24 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Precautions ==&lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
The safety of rabeprazole during pregnancy is unclear; it should only be used if clearly needed.&lt;br /&gt;
&lt;br /&gt;
=== Breastfeeding ===&lt;br /&gt;
It is unknown whether rabeprazole passes into breast milk; caution is advised.&lt;br /&gt;
&lt;br /&gt;
=== Children and Elderly ===&lt;br /&gt;
Rabeprazole can be used in children aged 12 years and older for GERD treatment. Use in elderly patients may require careful monitoring due to potential increased sensitivity to side effects.&lt;br /&gt;
&lt;br /&gt;
=== Monitoring Items ===&lt;br /&gt;
Patients on rabeprazole should be monitored for:&lt;br /&gt;
* Signs of gastrointestinal bleeding&lt;br /&gt;
* Electrolyte levels, particularly magnesium&lt;br /&gt;
&lt;br /&gt;
=== Drug Interactions ===&lt;br /&gt;
Rabeprazole may interact with other medications, including certain anticoagulants, antifungals, and antiretrovirals. It is important to inform healthcare providers about all medications being taken.&lt;br /&gt;
&lt;br /&gt;
== FAQ ==&lt;br /&gt;
&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
Take rabeprazole orally, usually once daily before a meal. Swallow the tablet whole without crushing or chewing.&lt;br /&gt;
&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid alcohol and NSAIDs unless directed by a healthcare provider, as they may increase the risk of gastrointestinal side effects.&lt;br /&gt;
&lt;br /&gt;
=== What happens if I miss a dose? ===&lt;br /&gt;
If you miss a dose, take it as soon as you remember. If it&#039;s almost time for your next dose, skip the missed dose and resume your regular schedule. Do not double the dose.&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5023</id>
		<title>Rabeprazole</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5023"/>
		<updated>2025-01-05T14:12:49Z</updated>

		<summary type="html">&lt;p&gt;Annayung: /* Dosages for Normal People */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
= Rabeprazole =&lt;br /&gt;
==Pronunciation==&lt;br /&gt;
===Rabeprazole 20mg===&lt;br /&gt;
[[File:Rabeprazole 20mg.mp3]]&lt;br /&gt;
&lt;br /&gt;
== Drug Class ==&lt;br /&gt;
Rabeprazole belongs to the class of medications known as &#039;&#039;&#039;proton pump inhibitors (PPIs)&#039;&#039;&#039;. These drugs work by inhibiting gastric acid secretion.&lt;br /&gt;
&lt;br /&gt;
== Common Strengths ==&lt;br /&gt;
Rabeprazole is available in the following strengths:&lt;br /&gt;
* 10 mg delayed-release tablets&lt;br /&gt;
* 20 mg delayed-release tablets&lt;br /&gt;
&lt;br /&gt;
== Drug Trade Name ==&lt;br /&gt;
Rabeprazole is marketed under the trade name &#039;&#039;&#039;PARIET&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Drug Usage ==&lt;br /&gt;
Rabeprazole is primarily used for:&lt;br /&gt;
* Healing of erosive or ulcerative gastroesophageal reflux disease (GERD)&lt;br /&gt;
* Maintenance of healing of erosive or ulcerative GERD&lt;br /&gt;
* Treatment of symptomatic GERD&lt;br /&gt;
* Healing of duodenal ulcers&lt;br /&gt;
* Eradication of &#039;&#039;Helicobacter pylori&#039;&#039; to reduce the risk of duodenal ulcer recurrence&lt;br /&gt;
* Treatment of pathological hypersecretory conditions, including Zollinger-Ellison syndrome&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Rabeprazole works by selectively and irreversibly inhibiting the H^+, K^+-ATPase enzyme system (the proton pump) at the secretory surface of gastric parietal cells. This inhibition reduces gastric acid secretion, thereby alleviating symptoms associated with excess stomach acid.&lt;br /&gt;
&lt;br /&gt;
== Route of Administration ==&lt;br /&gt;
Rabeprazole is administered orally, available as delayed-release tablets.&lt;br /&gt;
&lt;br /&gt;
== Dosages for Normal People ==&lt;br /&gt;
The typical dosage for adults is:&lt;br /&gt;
* &#039;&#039;&#039;GERD treatment:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks; maintenance 10-20 mg daily.&lt;br /&gt;
* &#039;&#039;&#039;Benign gastric ulcer:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks, dose to be taken in the morning.&lt;br /&gt;
* &#039;&#039;&#039;Duodenal ulcer:&#039;&#039;&#039; 20 mg once daily for 4 weeks, dose to be taken in the morning.&lt;br /&gt;
* &#039;&#039;&#039;Zollinger-Ellison syndrome:&#039;&#039;&#039; Initially 60 mg once daily, adjusted according to response, doses above 100 mg daily given in 2 divided doses; maximum 120 mg per day.&lt;br /&gt;
* &#039;&#039;&#039;H. pylori eradication:&#039;&#039;&#039; 20 mg twice daily.&lt;br /&gt;
&lt;br /&gt;
For renal dosing based on eGFR:&lt;br /&gt;
* No specific renal dose adjustment is typically required, but caution is advised in patients with severe renal impairment.&lt;br /&gt;
&lt;br /&gt;
== Side Effects: Common and Serious Side Effects ==&lt;br /&gt;
Common side effects include:&lt;br /&gt;
* Constipation&lt;br /&gt;
* Weakness&lt;br /&gt;
* Throat inflammation&lt;br /&gt;
&lt;br /&gt;
Serious side effects may include:&lt;br /&gt;
* Osteoporosis-related fractures&lt;br /&gt;
* Low blood magnesium levels&lt;br /&gt;
* &#039;&#039;Clostridioides difficile&#039;&#039; infection in the colon&lt;br /&gt;
* Pneumonia&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
Rabeprazole has an absolute bioavailability of approximately 52%. It undergoes hepatic metabolism and has a half-life of about 1 to 2 hours. The onset of action occurs within 1 hour, with a duration of action lasting up to 24 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Precautions ==&lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
The safety of rabeprazole during pregnancy is unclear; it should only be used if clearly needed.&lt;br /&gt;
&lt;br /&gt;
=== Breastfeeding ===&lt;br /&gt;
It is unknown whether rabeprazole passes into breast milk; caution is advised.&lt;br /&gt;
&lt;br /&gt;
=== Children and Elderly ===&lt;br /&gt;
Rabeprazole can be used in children aged 12 years and older for GERD treatment. Use in elderly patients may require careful monitoring due to potential increased sensitivity to side effects.&lt;br /&gt;
&lt;br /&gt;
=== Monitoring Items ===&lt;br /&gt;
Patients on rabeprazole should be monitored for:&lt;br /&gt;
* Signs of gastrointestinal bleeding&lt;br /&gt;
* Electrolyte levels, particularly magnesium&lt;br /&gt;
&lt;br /&gt;
=== Drug Interactions ===&lt;br /&gt;
Rabeprazole may interact with other medications, including certain anticoagulants, antifungals, and antiretrovirals. It is important to inform healthcare providers about all medications being taken.&lt;br /&gt;
&lt;br /&gt;
== FAQ ==&lt;br /&gt;
&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
Take rabeprazole orally, usually once daily before a meal. Swallow the tablet whole without crushing or chewing.&lt;br /&gt;
&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid alcohol and NSAIDs unless directed by a healthcare provider, as they may increase the risk of gastrointestinal side effects.&lt;br /&gt;
&lt;br /&gt;
=== What happens if I miss a dose? ===&lt;br /&gt;
If you miss a dose, take it as soon as you remember. If it&#039;s almost time for your next dose, skip the missed dose and resume your regular schedule. Do not double the dose.&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5022</id>
		<title>Rabeprazole</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5022"/>
		<updated>2025-01-05T14:06:14Z</updated>

		<summary type="html">&lt;p&gt;Annayung: /* Route of Administration */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
= Rabeprazole =&lt;br /&gt;
==Pronunciation==&lt;br /&gt;
===Rabeprazole 20mg===&lt;br /&gt;
[[File:Rabeprazole 20mg.mp3]]&lt;br /&gt;
&lt;br /&gt;
== Drug Class ==&lt;br /&gt;
Rabeprazole belongs to the class of medications known as &#039;&#039;&#039;proton pump inhibitors (PPIs)&#039;&#039;&#039;. These drugs work by inhibiting gastric acid secretion.&lt;br /&gt;
&lt;br /&gt;
== Common Strengths ==&lt;br /&gt;
Rabeprazole is available in the following strengths:&lt;br /&gt;
* 10 mg delayed-release tablets&lt;br /&gt;
* 20 mg delayed-release tablets&lt;br /&gt;
&lt;br /&gt;
== Drug Trade Name ==&lt;br /&gt;
Rabeprazole is marketed under the trade name &#039;&#039;&#039;PARIET&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Drug Usage ==&lt;br /&gt;
Rabeprazole is primarily used for:&lt;br /&gt;
* Healing of erosive or ulcerative gastroesophageal reflux disease (GERD)&lt;br /&gt;
* Maintenance of healing of erosive or ulcerative GERD&lt;br /&gt;
* Treatment of symptomatic GERD&lt;br /&gt;
* Healing of duodenal ulcers&lt;br /&gt;
* Eradication of &#039;&#039;Helicobacter pylori&#039;&#039; to reduce the risk of duodenal ulcer recurrence&lt;br /&gt;
* Treatment of pathological hypersecretory conditions, including Zollinger-Ellison syndrome&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Rabeprazole works by selectively and irreversibly inhibiting the H^+, K^+-ATPase enzyme system (the proton pump) at the secretory surface of gastric parietal cells. This inhibition reduces gastric acid secretion, thereby alleviating symptoms associated with excess stomach acid.&lt;br /&gt;
&lt;br /&gt;
== Route of Administration ==&lt;br /&gt;
Rabeprazole is administered orally, available as delayed-release tablets.&lt;br /&gt;
&lt;br /&gt;
== Dosages for Normal People ==&lt;br /&gt;
The typical dosage for adults is:&lt;br /&gt;
* &#039;&#039;&#039;GERD treatment:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks.&lt;br /&gt;
&lt;br /&gt;
For renal dosing based on eGFR:&lt;br /&gt;
* No specific renal dose adjustment is typically required, but caution is advised in patients with severe renal impairment.&lt;br /&gt;
&lt;br /&gt;
== Side Effects: Common and Serious Side Effects ==&lt;br /&gt;
Common side effects include:&lt;br /&gt;
* Constipation&lt;br /&gt;
* Weakness&lt;br /&gt;
* Throat inflammation&lt;br /&gt;
&lt;br /&gt;
Serious side effects may include:&lt;br /&gt;
* Osteoporosis-related fractures&lt;br /&gt;
* Low blood magnesium levels&lt;br /&gt;
* &#039;&#039;Clostridioides difficile&#039;&#039; infection in the colon&lt;br /&gt;
* Pneumonia&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
Rabeprazole has an absolute bioavailability of approximately 52%. It undergoes hepatic metabolism and has a half-life of about 1 to 2 hours. The onset of action occurs within 1 hour, with a duration of action lasting up to 24 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Precautions ==&lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
The safety of rabeprazole during pregnancy is unclear; it should only be used if clearly needed.&lt;br /&gt;
&lt;br /&gt;
=== Breastfeeding ===&lt;br /&gt;
It is unknown whether rabeprazole passes into breast milk; caution is advised.&lt;br /&gt;
&lt;br /&gt;
=== Children and Elderly ===&lt;br /&gt;
Rabeprazole can be used in children aged 12 years and older for GERD treatment. Use in elderly patients may require careful monitoring due to potential increased sensitivity to side effects.&lt;br /&gt;
&lt;br /&gt;
=== Monitoring Items ===&lt;br /&gt;
Patients on rabeprazole should be monitored for:&lt;br /&gt;
* Signs of gastrointestinal bleeding&lt;br /&gt;
* Electrolyte levels, particularly magnesium&lt;br /&gt;
&lt;br /&gt;
=== Drug Interactions ===&lt;br /&gt;
Rabeprazole may interact with other medications, including certain anticoagulants, antifungals, and antiretrovirals. It is important to inform healthcare providers about all medications being taken.&lt;br /&gt;
&lt;br /&gt;
== FAQ ==&lt;br /&gt;
&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
Take rabeprazole orally, usually once daily before a meal. Swallow the tablet whole without crushing or chewing.&lt;br /&gt;
&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid alcohol and NSAIDs unless directed by a healthcare provider, as they may increase the risk of gastrointestinal side effects.&lt;br /&gt;
&lt;br /&gt;
=== What happens if I miss a dose? ===&lt;br /&gt;
If you miss a dose, take it as soon as you remember. If it&#039;s almost time for your next dose, skip the missed dose and resume your regular schedule. Do not double the dose.&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5021</id>
		<title>Rabeprazole</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5021"/>
		<updated>2025-01-05T14:05:29Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
= Rabeprazole =&lt;br /&gt;
==Pronunciation==&lt;br /&gt;
===Rabeprazole 20mg===&lt;br /&gt;
[[File:Rabeprazole 20mg.mp3]]&lt;br /&gt;
&lt;br /&gt;
== Drug Class ==&lt;br /&gt;
Rabeprazole belongs to the class of medications known as &#039;&#039;&#039;proton pump inhibitors (PPIs)&#039;&#039;&#039;. These drugs work by inhibiting gastric acid secretion.&lt;br /&gt;
&lt;br /&gt;
== Common Strengths ==&lt;br /&gt;
Rabeprazole is available in the following strengths:&lt;br /&gt;
* 10 mg delayed-release tablets&lt;br /&gt;
* 20 mg delayed-release tablets&lt;br /&gt;
&lt;br /&gt;
== Drug Trade Name ==&lt;br /&gt;
Rabeprazole is marketed under the trade name &#039;&#039;&#039;PARIET&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Drug Usage ==&lt;br /&gt;
Rabeprazole is primarily used for:&lt;br /&gt;
* Healing of erosive or ulcerative gastroesophageal reflux disease (GERD)&lt;br /&gt;
* Maintenance of healing of erosive or ulcerative GERD&lt;br /&gt;
* Treatment of symptomatic GERD&lt;br /&gt;
* Healing of duodenal ulcers&lt;br /&gt;
* Eradication of &#039;&#039;Helicobacter pylori&#039;&#039; to reduce the risk of duodenal ulcer recurrence&lt;br /&gt;
* Treatment of pathological hypersecretory conditions, including Zollinger-Ellison syndrome&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Rabeprazole works by selectively and irreversibly inhibiting the H^+, K^+-ATPase enzyme system (the proton pump) at the secretory surface of gastric parietal cells. This inhibition reduces gastric acid secretion, thereby alleviating symptoms associated with excess stomach acid.&lt;br /&gt;
&lt;br /&gt;
== Route of Administration ==&lt;br /&gt;
Rabeprazole is administered orally, available as delayed-release tablets and capsules.&lt;br /&gt;
&lt;br /&gt;
== Dosages for Normal People ==&lt;br /&gt;
The typical dosage for adults is:&lt;br /&gt;
* &#039;&#039;&#039;GERD treatment:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks.&lt;br /&gt;
&lt;br /&gt;
For renal dosing based on eGFR:&lt;br /&gt;
* No specific renal dose adjustment is typically required, but caution is advised in patients with severe renal impairment.&lt;br /&gt;
&lt;br /&gt;
== Side Effects: Common and Serious Side Effects ==&lt;br /&gt;
Common side effects include:&lt;br /&gt;
* Constipation&lt;br /&gt;
* Weakness&lt;br /&gt;
* Throat inflammation&lt;br /&gt;
&lt;br /&gt;
Serious side effects may include:&lt;br /&gt;
* Osteoporosis-related fractures&lt;br /&gt;
* Low blood magnesium levels&lt;br /&gt;
* &#039;&#039;Clostridioides difficile&#039;&#039; infection in the colon&lt;br /&gt;
* Pneumonia&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
Rabeprazole has an absolute bioavailability of approximately 52%. It undergoes hepatic metabolism and has a half-life of about 1 to 2 hours. The onset of action occurs within 1 hour, with a duration of action lasting up to 24 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Precautions ==&lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
The safety of rabeprazole during pregnancy is unclear; it should only be used if clearly needed.&lt;br /&gt;
&lt;br /&gt;
=== Breastfeeding ===&lt;br /&gt;
It is unknown whether rabeprazole passes into breast milk; caution is advised.&lt;br /&gt;
&lt;br /&gt;
=== Children and Elderly ===&lt;br /&gt;
Rabeprazole can be used in children aged 12 years and older for GERD treatment. Use in elderly patients may require careful monitoring due to potential increased sensitivity to side effects.&lt;br /&gt;
&lt;br /&gt;
=== Monitoring Items ===&lt;br /&gt;
Patients on rabeprazole should be monitored for:&lt;br /&gt;
* Signs of gastrointestinal bleeding&lt;br /&gt;
* Electrolyte levels, particularly magnesium&lt;br /&gt;
&lt;br /&gt;
=== Drug Interactions ===&lt;br /&gt;
Rabeprazole may interact with other medications, including certain anticoagulants, antifungals, and antiretrovirals. It is important to inform healthcare providers about all medications being taken.&lt;br /&gt;
&lt;br /&gt;
== FAQ ==&lt;br /&gt;
&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
Take rabeprazole orally, usually once daily before a meal. Swallow the tablet whole without crushing or chewing.&lt;br /&gt;
&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid alcohol and NSAIDs unless directed by a healthcare provider, as they may increase the risk of gastrointestinal side effects.&lt;br /&gt;
&lt;br /&gt;
=== What happens if I miss a dose? ===&lt;br /&gt;
If you miss a dose, take it as soon as you remember. If it&#039;s almost time for your next dose, skip the missed dose and resume your regular schedule. Do not double the dose.&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5018</id>
		<title>Rabeprazole</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5018"/>
		<updated>2025-01-05T12:49:59Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
= Rabeprazole =&lt;br /&gt;
==Pronunciation==&lt;br /&gt;
===Rabeprazole 20mg===&lt;br /&gt;
[[File:Rabeprazole 20mg.mp3]]&lt;br /&gt;
&lt;br /&gt;
== Drug Class ==&lt;br /&gt;
Rabeprazole belongs to the class of medications known as &#039;&#039;&#039;proton pump inhibitors (PPIs)&#039;&#039;&#039;. These drugs work by inhibiting gastric acid secretion.&lt;br /&gt;
&lt;br /&gt;
== Common Strengths ==&lt;br /&gt;
Rabeprazole is available in the following strengths:&lt;br /&gt;
* 10 mg delayed-release tablets&lt;br /&gt;
* 20 mg delayed-release tablets&lt;br /&gt;
&lt;br /&gt;
== Drug Trade Name ==&lt;br /&gt;
Rabeprazole is marketed under the trade name &#039;&#039;&#039;Aciphex&#039;&#039;&#039;, among others.&lt;br /&gt;
&lt;br /&gt;
== Drug Usage ==&lt;br /&gt;
Rabeprazole is primarily used for:&lt;br /&gt;
* Healing of erosive or ulcerative gastroesophageal reflux disease (GERD)&lt;br /&gt;
* Maintenance of healing of erosive or ulcerative GERD&lt;br /&gt;
* Treatment of symptomatic GERD&lt;br /&gt;
* Healing of duodenal ulcers&lt;br /&gt;
* Eradication of &#039;&#039;Helicobacter pylori&#039;&#039; to reduce the risk of duodenal ulcer recurrence&lt;br /&gt;
* Treatment of pathological hypersecretory conditions, including Zollinger-Ellison syndrome&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Rabeprazole works by selectively and irreversibly inhibiting the H^+, K^+-ATPase enzyme system (the proton pump) at the secretory surface of gastric parietal cells. This inhibition reduces gastric acid secretion, thereby alleviating symptoms associated with excess stomach acid.&lt;br /&gt;
&lt;br /&gt;
== Route of Administration ==&lt;br /&gt;
Rabeprazole is administered orally, available as delayed-release tablets and capsules.&lt;br /&gt;
&lt;br /&gt;
== Dosages for Normal People ==&lt;br /&gt;
The typical dosage for adults is:&lt;br /&gt;
* &#039;&#039;&#039;GERD treatment:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks.&lt;br /&gt;
&lt;br /&gt;
For renal dosing based on eGFR:&lt;br /&gt;
* No specific renal dose adjustment is typically required, but caution is advised in patients with severe renal impairment.&lt;br /&gt;
&lt;br /&gt;
== Side Effects: Common and Serious Side Effects ==&lt;br /&gt;
Common side effects include:&lt;br /&gt;
* Constipation&lt;br /&gt;
* Weakness&lt;br /&gt;
* Throat inflammation&lt;br /&gt;
&lt;br /&gt;
Serious side effects may include:&lt;br /&gt;
* Osteoporosis-related fractures&lt;br /&gt;
* Low blood magnesium levels&lt;br /&gt;
* &#039;&#039;Clostridioides difficile&#039;&#039; infection in the colon&lt;br /&gt;
* Pneumonia&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
Rabeprazole has an absolute bioavailability of approximately 52%. It undergoes hepatic metabolism and has a half-life of about 1 to 2 hours. The onset of action occurs within 1 hour, with a duration of action lasting up to 24 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Precautions ==&lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
The safety of rabeprazole during pregnancy is unclear; it should only be used if clearly needed.&lt;br /&gt;
&lt;br /&gt;
=== Breastfeeding ===&lt;br /&gt;
It is unknown whether rabeprazole passes into breast milk; caution is advised.&lt;br /&gt;
&lt;br /&gt;
=== Children and Elderly ===&lt;br /&gt;
Rabeprazole can be used in children aged 12 years and older for GERD treatment. Use in elderly patients may require careful monitoring due to potential increased sensitivity to side effects.&lt;br /&gt;
&lt;br /&gt;
=== Monitoring Items ===&lt;br /&gt;
Patients on rabeprazole should be monitored for:&lt;br /&gt;
* Signs of gastrointestinal bleeding&lt;br /&gt;
* Electrolyte levels, particularly magnesium&lt;br /&gt;
&lt;br /&gt;
=== Drug Interactions ===&lt;br /&gt;
Rabeprazole may interact with other medications, including certain anticoagulants, antifungals, and antiretrovirals. It is important to inform healthcare providers about all medications being taken.&lt;br /&gt;
&lt;br /&gt;
== FAQ ==&lt;br /&gt;
&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
Take rabeprazole orally, usually once daily before a meal. Swallow the tablet whole without crushing or chewing.&lt;br /&gt;
&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid alcohol and NSAIDs unless directed by a healthcare provider, as they may increase the risk of gastrointestinal side effects.&lt;br /&gt;
&lt;br /&gt;
=== What happens if I miss a dose? ===&lt;br /&gt;
If you miss a dose, take it as soon as you remember. If it&#039;s almost time for your next dose, skip the missed dose and resume your regular schedule. Do not double the dose.&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5017</id>
		<title>Rabeprazole</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5017"/>
		<updated>2025-01-05T12:49:38Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]][[Category: GI]]&lt;br /&gt;
= Rabeprazole =&lt;br /&gt;
==Pronunciation==&lt;br /&gt;
===Rabeprazole 20mg===&lt;br /&gt;
[[File:Rabeprazole 20mg.mp3]]&lt;br /&gt;
&lt;br /&gt;
== Drug Class ==&lt;br /&gt;
Rabeprazole belongs to the class of medications known as &#039;&#039;&#039;proton pump inhibitors (PPIs)&#039;&#039;&#039;. These drugs work by inhibiting gastric acid secretion.&lt;br /&gt;
&lt;br /&gt;
== Common Strengths ==&lt;br /&gt;
Rabeprazole is available in the following strengths:&lt;br /&gt;
* 10 mg delayed-release tablets&lt;br /&gt;
* 20 mg delayed-release tablets&lt;br /&gt;
&lt;br /&gt;
== Drug Trade Name ==&lt;br /&gt;
Rabeprazole is marketed under the trade name &#039;&#039;&#039;Aciphex&#039;&#039;&#039;, among others.&lt;br /&gt;
&lt;br /&gt;
== Drug Usage ==&lt;br /&gt;
Rabeprazole is primarily used for:&lt;br /&gt;
* Healing of erosive or ulcerative gastroesophageal reflux disease (GERD)&lt;br /&gt;
* Maintenance of healing of erosive or ulcerative GERD&lt;br /&gt;
* Treatment of symptomatic GERD&lt;br /&gt;
* Healing of duodenal ulcers&lt;br /&gt;
* Eradication of &#039;&#039;Helicobacter pylori&#039;&#039; to reduce the risk of duodenal ulcer recurrence&lt;br /&gt;
* Treatment of pathological hypersecretory conditions, including Zollinger-Ellison syndrome&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Rabeprazole works by selectively and irreversibly inhibiting the H^+, K^+-ATPase enzyme system (the proton pump) at the secretory surface of gastric parietal cells. This inhibition reduces gastric acid secretion, thereby alleviating symptoms associated with excess stomach acid.&lt;br /&gt;
&lt;br /&gt;
== Route of Administration ==&lt;br /&gt;
Rabeprazole is administered orally, available as delayed-release tablets and capsules.&lt;br /&gt;
&lt;br /&gt;
== Dosages for Normal People ==&lt;br /&gt;
The typical dosage for adults is:&lt;br /&gt;
* &#039;&#039;&#039;GERD treatment:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks.&lt;br /&gt;
&lt;br /&gt;
For renal dosing based on eGFR:&lt;br /&gt;
* No specific renal dose adjustment is typically required, but caution is advised in patients with severe renal impairment.&lt;br /&gt;
&lt;br /&gt;
== Side Effects: Common and Serious Side Effects ==&lt;br /&gt;
Common side effects include:&lt;br /&gt;
* Constipation&lt;br /&gt;
* Weakness&lt;br /&gt;
* Throat inflammation&lt;br /&gt;
&lt;br /&gt;
Serious side effects may include:&lt;br /&gt;
* Osteoporosis-related fractures&lt;br /&gt;
* Low blood magnesium levels&lt;br /&gt;
* &#039;&#039;Clostridioides difficile&#039;&#039; infection in the colon&lt;br /&gt;
* Pneumonia&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
Rabeprazole has an absolute bioavailability of approximately 52%. It undergoes hepatic metabolism and has a half-life of about 1 to 2 hours. The onset of action occurs within 1 hour, with a duration of action lasting up to 24 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Precautions ==&lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
The safety of rabeprazole during pregnancy is unclear; it should only be used if clearly needed.&lt;br /&gt;
&lt;br /&gt;
=== Breastfeeding ===&lt;br /&gt;
It is unknown whether rabeprazole passes into breast milk; caution is advised.&lt;br /&gt;
&lt;br /&gt;
=== Children and Elderly ===&lt;br /&gt;
Rabeprazole can be used in children aged 12 years and older for GERD treatment. Use in elderly patients may require careful monitoring due to potential increased sensitivity to side effects.&lt;br /&gt;
&lt;br /&gt;
=== Monitoring Items ===&lt;br /&gt;
Patients on rabeprazole should be monitored for:&lt;br /&gt;
* Signs of gastrointestinal bleeding&lt;br /&gt;
* Electrolyte levels, particularly magnesium&lt;br /&gt;
&lt;br /&gt;
=== Drug Interactions ===&lt;br /&gt;
Rabeprazole may interact with other medications, including certain anticoagulants, antifungals, and antiretrovirals. It is important to inform healthcare providers about all medications being taken.&lt;br /&gt;
&lt;br /&gt;
== FAQ ==&lt;br /&gt;
&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
Take rabeprazole orally, usually once daily before a meal. Swallow the tablet whole without crushing or chewing.&lt;br /&gt;
&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid alcohol and NSAIDs unless directed by a healthcare provider, as they may increase the risk of gastrointestinal side effects.&lt;br /&gt;
&lt;br /&gt;
=== What happens if I miss a dose? ===&lt;br /&gt;
If you miss a dose, take it as soon as you remember. If it&#039;s almost time for your next dose, skip the missed dose and resume your regular schedule. Do not double the dose.&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5016</id>
		<title>Rabeprazole</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5016"/>
		<updated>2025-01-05T12:47:03Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
= Rabeprazole =&lt;br /&gt;
==Pronunciation==&lt;br /&gt;
===Rabeprazole 20mg===&lt;br /&gt;
[[File:Rabeprazole 20mg.mp3]]&lt;br /&gt;
&lt;br /&gt;
== Drug Class ==&lt;br /&gt;
Rabeprazole belongs to the class of medications known as &#039;&#039;&#039;proton pump inhibitors (PPIs)&#039;&#039;&#039;. These drugs work by inhibiting gastric acid secretion.&lt;br /&gt;
&lt;br /&gt;
== Common Strengths ==&lt;br /&gt;
Rabeprazole is available in the following strengths:&lt;br /&gt;
* 10 mg delayed-release tablets&lt;br /&gt;
* 20 mg delayed-release tablets&lt;br /&gt;
&lt;br /&gt;
== Drug Trade Name ==&lt;br /&gt;
Rabeprazole is marketed under the trade name &#039;&#039;&#039;Aciphex&#039;&#039;&#039;, among others.&lt;br /&gt;
&lt;br /&gt;
== Drug Usage ==&lt;br /&gt;
Rabeprazole is primarily used for:&lt;br /&gt;
* Healing of erosive or ulcerative gastroesophageal reflux disease (GERD)&lt;br /&gt;
* Maintenance of healing of erosive or ulcerative GERD&lt;br /&gt;
* Treatment of symptomatic GERD&lt;br /&gt;
* Healing of duodenal ulcers&lt;br /&gt;
* Eradication of &#039;&#039;Helicobacter pylori&#039;&#039; to reduce the risk of duodenal ulcer recurrence&lt;br /&gt;
* Treatment of pathological hypersecretory conditions, including Zollinger-Ellison syndrome&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Rabeprazole works by selectively and irreversibly inhibiting the H^+, K^+-ATPase enzyme system (the proton pump) at the secretory surface of gastric parietal cells. This inhibition reduces gastric acid secretion, thereby alleviating symptoms associated with excess stomach acid.&lt;br /&gt;
&lt;br /&gt;
== Route of Administration ==&lt;br /&gt;
Rabeprazole is administered orally, available as delayed-release tablets and capsules.&lt;br /&gt;
&lt;br /&gt;
== Dosages for Normal People ==&lt;br /&gt;
The typical dosage for adults is:&lt;br /&gt;
* &#039;&#039;&#039;GERD treatment:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks.&lt;br /&gt;
&lt;br /&gt;
For renal dosing based on eGFR:&lt;br /&gt;
* No specific renal dose adjustment is typically required, but caution is advised in patients with severe renal impairment.&lt;br /&gt;
&lt;br /&gt;
== Side Effects: Common and Serious Side Effects ==&lt;br /&gt;
Common side effects include:&lt;br /&gt;
* Constipation&lt;br /&gt;
* Weakness&lt;br /&gt;
* Throat inflammation&lt;br /&gt;
&lt;br /&gt;
Serious side effects may include:&lt;br /&gt;
* Osteoporosis-related fractures&lt;br /&gt;
* Low blood magnesium levels&lt;br /&gt;
* &#039;&#039;Clostridioides difficile&#039;&#039; infection in the colon&lt;br /&gt;
* Pneumonia&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
Rabeprazole has an absolute bioavailability of approximately 52%. It undergoes hepatic metabolism and has a half-life of about 1 to 2 hours. The onset of action occurs within 1 hour, with a duration of action lasting up to 24 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Precautions ==&lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
The safety of rabeprazole during pregnancy is unclear; it should only be used if clearly needed.&lt;br /&gt;
&lt;br /&gt;
=== Breastfeeding ===&lt;br /&gt;
It is unknown whether rabeprazole passes into breast milk; caution is advised.&lt;br /&gt;
&lt;br /&gt;
=== Children and Elderly ===&lt;br /&gt;
Rabeprazole can be used in children aged 12 years and older for GERD treatment. Use in elderly patients may require careful monitoring due to potential increased sensitivity to side effects.&lt;br /&gt;
&lt;br /&gt;
=== Monitoring Items ===&lt;br /&gt;
Patients on rabeprazole should be monitored for:&lt;br /&gt;
* Signs of gastrointestinal bleeding&lt;br /&gt;
* Electrolyte levels, particularly magnesium&lt;br /&gt;
&lt;br /&gt;
=== Drug Interactions ===&lt;br /&gt;
Rabeprazole may interact with other medications, including certain anticoagulants, antifungals, and antiretrovirals. It is important to inform healthcare providers about all medications being taken.&lt;br /&gt;
&lt;br /&gt;
== FAQ ==&lt;br /&gt;
&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
Take rabeprazole orally, usually once daily before a meal. Swallow the tablet whole without crushing or chewing.&lt;br /&gt;
&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid alcohol and NSAIDs unless directed by a healthcare provider, as they may increase the risk of gastrointestinal side effects.&lt;br /&gt;
&lt;br /&gt;
=== What happens if I miss a dose? ===&lt;br /&gt;
If you miss a dose, take it as soon as you remember. If it&#039;s almost time for your next dose, skip the missed dose and resume your regular schedule. Do not double the dose.&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5015</id>
		<title>Rabeprazole</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Rabeprazole&amp;diff=5015"/>
		<updated>2025-01-05T12:45:47Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
= Rabeprazole =&lt;br /&gt;
&lt;br /&gt;
== Drug Class ==&lt;br /&gt;
Rabeprazole belongs to the class of medications known as &#039;&#039;&#039;proton pump inhibitors (PPIs)&#039;&#039;&#039;. These drugs work by inhibiting gastric acid secretion.&lt;br /&gt;
&lt;br /&gt;
== Common Strengths ==&lt;br /&gt;
Rabeprazole is available in the following strengths:&lt;br /&gt;
* 10 mg delayed-release tablets&lt;br /&gt;
* 20 mg delayed-release tablets&lt;br /&gt;
&lt;br /&gt;
== Drug Trade Name ==&lt;br /&gt;
Rabeprazole is marketed under the trade name &#039;&#039;&#039;Aciphex&#039;&#039;&#039;, among others.&lt;br /&gt;
&lt;br /&gt;
== Drug Usage ==&lt;br /&gt;
Rabeprazole is primarily used for:&lt;br /&gt;
* Healing of erosive or ulcerative gastroesophageal reflux disease (GERD)&lt;br /&gt;
* Maintenance of healing of erosive or ulcerative GERD&lt;br /&gt;
* Treatment of symptomatic GERD&lt;br /&gt;
* Healing of duodenal ulcers&lt;br /&gt;
* Eradication of &#039;&#039;Helicobacter pylori&#039;&#039; to reduce the risk of duodenal ulcer recurrence&lt;br /&gt;
* Treatment of pathological hypersecretory conditions, including Zollinger-Ellison syndrome&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Rabeprazole works by selectively and irreversibly inhibiting the H^+, K^+-ATPase enzyme system (the proton pump) at the secretory surface of gastric parietal cells. This inhibition reduces gastric acid secretion, thereby alleviating symptoms associated with excess stomach acid.&lt;br /&gt;
&lt;br /&gt;
== Route of Administration ==&lt;br /&gt;
Rabeprazole is administered orally, available as delayed-release tablets and capsules.&lt;br /&gt;
&lt;br /&gt;
== Dosages for Normal People ==&lt;br /&gt;
The typical dosage for adults is:&lt;br /&gt;
* &#039;&#039;&#039;GERD treatment:&#039;&#039;&#039; 20 mg once daily for up to 8 weeks.&lt;br /&gt;
&lt;br /&gt;
For renal dosing based on eGFR:&lt;br /&gt;
* No specific renal dose adjustment is typically required, but caution is advised in patients with severe renal impairment.&lt;br /&gt;
&lt;br /&gt;
== Side Effects: Common and Serious Side Effects ==&lt;br /&gt;
Common side effects include:&lt;br /&gt;
* Constipation&lt;br /&gt;
* Weakness&lt;br /&gt;
* Throat inflammation&lt;br /&gt;
&lt;br /&gt;
Serious side effects may include:&lt;br /&gt;
* Osteoporosis-related fractures&lt;br /&gt;
* Low blood magnesium levels&lt;br /&gt;
* &#039;&#039;Clostridioides difficile&#039;&#039; infection in the colon&lt;br /&gt;
* Pneumonia&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
Rabeprazole has an absolute bioavailability of approximately 52%. It undergoes hepatic metabolism and has a half-life of about 1 to 2 hours. The onset of action occurs within 1 hour, with a duration of action lasting up to 24 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Precautions ==&lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
The safety of rabeprazole during pregnancy is unclear; it should only be used if clearly needed.&lt;br /&gt;
&lt;br /&gt;
=== Breastfeeding ===&lt;br /&gt;
It is unknown whether rabeprazole passes into breast milk; caution is advised.&lt;br /&gt;
&lt;br /&gt;
=== Children and Elderly ===&lt;br /&gt;
Rabeprazole can be used in children aged 12 years and older for GERD treatment. Use in elderly patients may require careful monitoring due to potential increased sensitivity to side effects.&lt;br /&gt;
&lt;br /&gt;
=== Monitoring Items ===&lt;br /&gt;
Patients on rabeprazole should be monitored for:&lt;br /&gt;
* Signs of gastrointestinal bleeding&lt;br /&gt;
* Electrolyte levels, particularly magnesium&lt;br /&gt;
&lt;br /&gt;
=== Drug Interactions ===&lt;br /&gt;
Rabeprazole may interact with other medications, including certain anticoagulants, antifungals, and antiretrovirals. It is important to inform healthcare providers about all medications being taken.&lt;br /&gt;
&lt;br /&gt;
== FAQ ==&lt;br /&gt;
&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
Take rabeprazole orally, usually once daily before a meal. Swallow the tablet whole without crushing or chewing.&lt;br /&gt;
&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid alcohol and NSAIDs unless directed by a healthcare provider, as they may increase the risk of gastrointestinal side effects.&lt;br /&gt;
&lt;br /&gt;
=== What happens if I miss a dose? ===&lt;br /&gt;
If you miss a dose, take it as soon as you remember. If it&#039;s almost time for your next dose, skip the missed dose and resume your regular schedule. Do not double the dose.&lt;br /&gt;
&lt;br /&gt;
==Pronunciation==&lt;br /&gt;
===Rabeprazole 20mg===&lt;br /&gt;
[[File:Rabeprazole 20mg.mp3]]&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Dexlansoprazole_(DEXILANT)&amp;diff=5014</id>
		<title>Dexlansoprazole (DEXILANT)</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Dexlansoprazole_(DEXILANT)&amp;diff=5014"/>
		<updated>2025-01-05T12:42:02Z</updated>

		<summary type="html">&lt;p&gt;Annayung: /* Drug Class */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]][[Category: Proton Pump Inhibitors (PPI)]][[:Category: Gastrointestinal Drug | &#039;&#039;&#039;Gastrointestinal Drug&#039;&#039;&#039;]] &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Drug class: [[:Category: Proton Pump Inhibitors (PPI) | Proton Pump Inhibitors (PPI)]]&#039;&#039;&#039; &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Dexlansoprazole&#039;&#039;&#039; (中文: [[右蘭索拉唑]]) &lt;br /&gt;
&lt;br /&gt;
==Drug Class== &lt;br /&gt;
&lt;br /&gt;
Proton Pump Inhibitor (PPI)&lt;br /&gt;
&lt;br /&gt;
==Common Strengths== &lt;br /&gt;
&lt;br /&gt;
*30 mg delayed-release capsules &lt;br /&gt;
&lt;br /&gt;
*60mg delayed-release capsules &lt;br /&gt;
&lt;br /&gt;
==Drug Trade Name== &lt;br /&gt;
&lt;br /&gt;
Dexilant &lt;br /&gt;
&lt;br /&gt;
==Drug Usage== &lt;br /&gt;
&lt;br /&gt;
*Healing of erosive esophagitis (EE) &lt;br /&gt;
&lt;br /&gt;
*Maintenance of healed erosive esophagitis (EE) &lt;br /&gt;
&lt;br /&gt;
*Treatment of gastroesophageal reflux disease (GERD)&lt;br /&gt;
&lt;br /&gt;
==Mechanism of Action== &lt;br /&gt;
&lt;br /&gt;
Inhibits (H+/K+ )-ATPase enzyme in the gastric parietal cells, blocking gastric acid production in the stomach &lt;br /&gt;
&lt;br /&gt;
==Route of Administration== &lt;br /&gt;
&lt;br /&gt;
Oral  &lt;br /&gt;
&lt;br /&gt;
==Dosages == &lt;br /&gt;
&lt;br /&gt;
For adults and children aged 12 years and older, the typical dosage is: &lt;br /&gt;
&lt;br /&gt;
Healing: 60 mg once daily for up to 8 weeks &lt;br /&gt;
&lt;br /&gt;
Maintenance: 30 mg once daily for up to 6 months &lt;br /&gt;
&lt;br /&gt;
GERD: 30 mg once daily for up to 4 weeks &lt;br /&gt;
&lt;br /&gt;
==Renal Dose Adjustments== &lt;br /&gt;
&lt;br /&gt;
No renal dose adjustment recommended &lt;br /&gt;
&lt;br /&gt;
==Common Side Effects== &lt;br /&gt;
&lt;br /&gt;
Diarrhea &lt;br /&gt;
&lt;br /&gt;
Abdominal pain &lt;br /&gt;
&lt;br /&gt;
Nausea &lt;br /&gt;
&lt;br /&gt;
Vomiting &lt;br /&gt;
&lt;br /&gt;
Flatulence &lt;br /&gt;
&lt;br /&gt;
==Serious Side Effects== &lt;br /&gt;
&lt;br /&gt;
Bone fractures &lt;br /&gt;
&lt;br /&gt;
Low blood magnesium levels &lt;br /&gt;
&lt;br /&gt;
Clostridium difficile infection &lt;br /&gt;
&lt;br /&gt;
Anaphylaxis &lt;br /&gt;
&lt;br /&gt;
Vitamin B12 deficiency &lt;br /&gt;
&lt;br /&gt;
==Pharmacokinetics== &lt;br /&gt;
&lt;br /&gt;
Dual-release mechanism &lt;br /&gt;
&lt;br /&gt;
Onset of action: 1-2 hours (first peak), 4-5 hours (second peak);  &lt;br /&gt;
&lt;br /&gt;
Duration of action: Up to 24 hours, longer than other PPIs &lt;br /&gt;
&lt;br /&gt;
==Drug Precautions== &lt;br /&gt;
&lt;br /&gt;
Pregnancy: Caution advised; Children: Safety not established; Elderly: Monitoring recommended &lt;br /&gt;
&lt;br /&gt;
Breastfeeding: safety during breastfeeding is unclear &lt;br /&gt;
&lt;br /&gt;
Children and Elderly: Approved for use in children aged 12 years and older; elderly patients may require monitoring due to potential increased sensitivity. &lt;br /&gt;
&lt;br /&gt;
==Monitoring Items== &lt;br /&gt;
&lt;br /&gt;
Regular monitoring of magnesium and vitamin B12 levels &lt;br /&gt;
&lt;br /&gt;
==Drug Interactions== &lt;br /&gt;
&lt;br /&gt;
Dexlansoprazole can interact with drugs metabolized by CYP2C19 and CYP3A4 enzymes &lt;br /&gt;
&lt;br /&gt;
Interacts with methotrexate, digoxin, warfarin, certain antiretrovirals &lt;br /&gt;
&lt;br /&gt;
==FAQ== &lt;br /&gt;
&lt;br /&gt;
==How should I take the tablet?== &lt;br /&gt;
&lt;br /&gt;
Take with or without food; swallow whole or sprinkle on apple sauce/water &lt;br /&gt;
&lt;br /&gt;
==What should I avoid while taking?== &lt;br /&gt;
&lt;br /&gt;
Avoid highly acidic foods and grapefruit &lt;br /&gt;
&lt;br /&gt;
==What happens if I miss a dose?== &lt;br /&gt;
&lt;br /&gt;
Take as soon as remembered unless close to next dose; do not double up on doses&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Dexlansoprazole_(DEXILANT)&amp;diff=5013</id>
		<title>Dexlansoprazole (DEXILANT)</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Dexlansoprazole_(DEXILANT)&amp;diff=5013"/>
		<updated>2025-01-05T12:41:47Z</updated>

		<summary type="html">&lt;p&gt;Annayung: /* Drug Class */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]][[Category: Proton Pump Inhibitors (PPI)]][[:Category: Gastrointestinal Drug | &#039;&#039;&#039;Gastrointestinal Drug&#039;&#039;&#039;]] &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Drug class: [[:Category: Proton Pump Inhibitors (PPI) | Proton Pump Inhibitors (PPI)]]&#039;&#039;&#039; &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Dexlansoprazole&#039;&#039;&#039; (中文: [[右蘭索拉唑]]) &lt;br /&gt;
&lt;br /&gt;
==Drug Class== &lt;br /&gt;
&lt;br /&gt;
Proton Pump Inhibitor (PPI) some text&lt;br /&gt;
&lt;br /&gt;
==Common Strengths== &lt;br /&gt;
&lt;br /&gt;
*30 mg delayed-release capsules &lt;br /&gt;
&lt;br /&gt;
*60mg delayed-release capsules &lt;br /&gt;
&lt;br /&gt;
==Drug Trade Name== &lt;br /&gt;
&lt;br /&gt;
Dexilant &lt;br /&gt;
&lt;br /&gt;
==Drug Usage== &lt;br /&gt;
&lt;br /&gt;
*Healing of erosive esophagitis (EE) &lt;br /&gt;
&lt;br /&gt;
*Maintenance of healed erosive esophagitis (EE) &lt;br /&gt;
&lt;br /&gt;
*Treatment of gastroesophageal reflux disease (GERD)&lt;br /&gt;
&lt;br /&gt;
==Mechanism of Action== &lt;br /&gt;
&lt;br /&gt;
Inhibits (H+/K+ )-ATPase enzyme in the gastric parietal cells, blocking gastric acid production in the stomach &lt;br /&gt;
&lt;br /&gt;
==Route of Administration== &lt;br /&gt;
&lt;br /&gt;
Oral  &lt;br /&gt;
&lt;br /&gt;
==Dosages == &lt;br /&gt;
&lt;br /&gt;
For adults and children aged 12 years and older, the typical dosage is: &lt;br /&gt;
&lt;br /&gt;
Healing: 60 mg once daily for up to 8 weeks &lt;br /&gt;
&lt;br /&gt;
Maintenance: 30 mg once daily for up to 6 months &lt;br /&gt;
&lt;br /&gt;
GERD: 30 mg once daily for up to 4 weeks &lt;br /&gt;
&lt;br /&gt;
==Renal Dose Adjustments== &lt;br /&gt;
&lt;br /&gt;
No renal dose adjustment recommended &lt;br /&gt;
&lt;br /&gt;
==Common Side Effects== &lt;br /&gt;
&lt;br /&gt;
Diarrhea &lt;br /&gt;
&lt;br /&gt;
Abdominal pain &lt;br /&gt;
&lt;br /&gt;
Nausea &lt;br /&gt;
&lt;br /&gt;
Vomiting &lt;br /&gt;
&lt;br /&gt;
Flatulence &lt;br /&gt;
&lt;br /&gt;
==Serious Side Effects== &lt;br /&gt;
&lt;br /&gt;
Bone fractures &lt;br /&gt;
&lt;br /&gt;
Low blood magnesium levels &lt;br /&gt;
&lt;br /&gt;
Clostridium difficile infection &lt;br /&gt;
&lt;br /&gt;
Anaphylaxis &lt;br /&gt;
&lt;br /&gt;
Vitamin B12 deficiency &lt;br /&gt;
&lt;br /&gt;
==Pharmacokinetics== &lt;br /&gt;
&lt;br /&gt;
Dual-release mechanism &lt;br /&gt;
&lt;br /&gt;
Onset of action: 1-2 hours (first peak), 4-5 hours (second peak);  &lt;br /&gt;
&lt;br /&gt;
Duration of action: Up to 24 hours, longer than other PPIs &lt;br /&gt;
&lt;br /&gt;
==Drug Precautions== &lt;br /&gt;
&lt;br /&gt;
Pregnancy: Caution advised; Children: Safety not established; Elderly: Monitoring recommended &lt;br /&gt;
&lt;br /&gt;
Breastfeeding: safety during breastfeeding is unclear &lt;br /&gt;
&lt;br /&gt;
Children and Elderly: Approved for use in children aged 12 years and older; elderly patients may require monitoring due to potential increased sensitivity. &lt;br /&gt;
&lt;br /&gt;
==Monitoring Items== &lt;br /&gt;
&lt;br /&gt;
Regular monitoring of magnesium and vitamin B12 levels &lt;br /&gt;
&lt;br /&gt;
==Drug Interactions== &lt;br /&gt;
&lt;br /&gt;
Dexlansoprazole can interact with drugs metabolized by CYP2C19 and CYP3A4 enzymes &lt;br /&gt;
&lt;br /&gt;
Interacts with methotrexate, digoxin, warfarin, certain antiretrovirals &lt;br /&gt;
&lt;br /&gt;
==FAQ== &lt;br /&gt;
&lt;br /&gt;
==How should I take the tablet?== &lt;br /&gt;
&lt;br /&gt;
Take with or without food; swallow whole or sprinkle on apple sauce/water &lt;br /&gt;
&lt;br /&gt;
==What should I avoid while taking?== &lt;br /&gt;
&lt;br /&gt;
Avoid highly acidic foods and grapefruit &lt;br /&gt;
&lt;br /&gt;
==What happens if I miss a dose?== &lt;br /&gt;
&lt;br /&gt;
Take as soon as remembered unless close to next dose; do not double up on doses&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Dexlansoprazole_(DEXILANT)&amp;diff=5012</id>
		<title>Dexlansoprazole (DEXILANT)</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Dexlansoprazole_(DEXILANT)&amp;diff=5012"/>
		<updated>2025-01-05T12:41:24Z</updated>

		<summary type="html">&lt;p&gt;Annayung: /* Drug Usage */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]][[Category: Proton Pump Inhibitors (PPI)]][[:Category: Gastrointestinal Drug | &#039;&#039;&#039;Gastrointestinal Drug&#039;&#039;&#039;]] &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Drug class: [[:Category: Proton Pump Inhibitors (PPI) | Proton Pump Inhibitors (PPI)]]&#039;&#039;&#039; &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Dexlansoprazole&#039;&#039;&#039; (中文: [[右蘭索拉唑]]) &lt;br /&gt;
&lt;br /&gt;
==Drug Class== &lt;br /&gt;
&lt;br /&gt;
Proton Pump Inhibitor (PPI) &lt;br /&gt;
&lt;br /&gt;
==Common Strengths== &lt;br /&gt;
&lt;br /&gt;
*30 mg delayed-release capsules &lt;br /&gt;
&lt;br /&gt;
*60mg delayed-release capsules &lt;br /&gt;
&lt;br /&gt;
==Drug Trade Name== &lt;br /&gt;
&lt;br /&gt;
Dexilant &lt;br /&gt;
&lt;br /&gt;
==Drug Usage== &lt;br /&gt;
&lt;br /&gt;
*Healing of erosive esophagitis (EE) &lt;br /&gt;
&lt;br /&gt;
*Maintenance of healed erosive esophagitis (EE) &lt;br /&gt;
&lt;br /&gt;
*Treatment of gastroesophageal reflux disease (GERD)&lt;br /&gt;
&lt;br /&gt;
==Mechanism of Action== &lt;br /&gt;
&lt;br /&gt;
Inhibits (H+/K+ )-ATPase enzyme in the gastric parietal cells, blocking gastric acid production in the stomach &lt;br /&gt;
&lt;br /&gt;
==Route of Administration== &lt;br /&gt;
&lt;br /&gt;
Oral  &lt;br /&gt;
&lt;br /&gt;
==Dosages == &lt;br /&gt;
&lt;br /&gt;
For adults and children aged 12 years and older, the typical dosage is: &lt;br /&gt;
&lt;br /&gt;
Healing: 60 mg once daily for up to 8 weeks &lt;br /&gt;
&lt;br /&gt;
Maintenance: 30 mg once daily for up to 6 months &lt;br /&gt;
&lt;br /&gt;
GERD: 30 mg once daily for up to 4 weeks &lt;br /&gt;
&lt;br /&gt;
==Renal Dose Adjustments== &lt;br /&gt;
&lt;br /&gt;
No renal dose adjustment recommended &lt;br /&gt;
&lt;br /&gt;
==Common Side Effects== &lt;br /&gt;
&lt;br /&gt;
Diarrhea &lt;br /&gt;
&lt;br /&gt;
Abdominal pain &lt;br /&gt;
&lt;br /&gt;
Nausea &lt;br /&gt;
&lt;br /&gt;
Vomiting &lt;br /&gt;
&lt;br /&gt;
Flatulence &lt;br /&gt;
&lt;br /&gt;
==Serious Side Effects== &lt;br /&gt;
&lt;br /&gt;
Bone fractures &lt;br /&gt;
&lt;br /&gt;
Low blood magnesium levels &lt;br /&gt;
&lt;br /&gt;
Clostridium difficile infection &lt;br /&gt;
&lt;br /&gt;
Anaphylaxis &lt;br /&gt;
&lt;br /&gt;
Vitamin B12 deficiency &lt;br /&gt;
&lt;br /&gt;
==Pharmacokinetics== &lt;br /&gt;
&lt;br /&gt;
Dual-release mechanism &lt;br /&gt;
&lt;br /&gt;
Onset of action: 1-2 hours (first peak), 4-5 hours (second peak);  &lt;br /&gt;
&lt;br /&gt;
Duration of action: Up to 24 hours, longer than other PPIs &lt;br /&gt;
&lt;br /&gt;
==Drug Precautions== &lt;br /&gt;
&lt;br /&gt;
Pregnancy: Caution advised; Children: Safety not established; Elderly: Monitoring recommended &lt;br /&gt;
&lt;br /&gt;
Breastfeeding: safety during breastfeeding is unclear &lt;br /&gt;
&lt;br /&gt;
Children and Elderly: Approved for use in children aged 12 years and older; elderly patients may require monitoring due to potential increased sensitivity. &lt;br /&gt;
&lt;br /&gt;
==Monitoring Items== &lt;br /&gt;
&lt;br /&gt;
Regular monitoring of magnesium and vitamin B12 levels &lt;br /&gt;
&lt;br /&gt;
==Drug Interactions== &lt;br /&gt;
&lt;br /&gt;
Dexlansoprazole can interact with drugs metabolized by CYP2C19 and CYP3A4 enzymes &lt;br /&gt;
&lt;br /&gt;
Interacts with methotrexate, digoxin, warfarin, certain antiretrovirals &lt;br /&gt;
&lt;br /&gt;
==FAQ== &lt;br /&gt;
&lt;br /&gt;
==How should I take the tablet?== &lt;br /&gt;
&lt;br /&gt;
Take with or without food; swallow whole or sprinkle on apple sauce/water &lt;br /&gt;
&lt;br /&gt;
==What should I avoid while taking?== &lt;br /&gt;
&lt;br /&gt;
Avoid highly acidic foods and grapefruit &lt;br /&gt;
&lt;br /&gt;
==What happens if I miss a dose?== &lt;br /&gt;
&lt;br /&gt;
Take as soon as remembered unless close to next dose; do not double up on doses&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Morphine&amp;diff=2063</id>
		<title>Morphine</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Morphine&amp;diff=2063"/>
		<updated>2020-10-11T13:15:48Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]] [[Category: Non-opioid Analgesic]] [[Category: Pain relief]]&lt;br /&gt;
&#039;&#039;&#039;Morphine&#039;&#039;&#039; is an opioid analgesic with agonist activity mainly at μ opioid receptors. Morphine is used for the relief of moderate to severe pain, especially that associated with cancer, myocardial infarction and surgery. &lt;br /&gt;
==Drug Names==&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Generic Name 藥名&lt;br /&gt;
!HA Code 藥物代碼&lt;br /&gt;
!Classification藥物分類&lt;br /&gt;
|-&lt;br /&gt;
|Morphine Syrup&lt;br /&gt;
|MORP26&lt;br /&gt;
|DD&lt;br /&gt;
|-&lt;br /&gt;
|Morphine SR Tab 10mg&lt;br /&gt;
|MORP04&lt;br /&gt;
|DD&lt;br /&gt;
|-&lt;br /&gt;
|Morphine SR Tab 30mg&lt;br /&gt;
|MORP05&lt;br /&gt;
|DD&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Mechanism of Action==&lt;br /&gt;
Pain relief, Opioid analgesic.&lt;br /&gt;
&lt;br /&gt;
Equivalent doses of opioid analgesics.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Analgesic / Route&lt;br /&gt;
!Dose&lt;br /&gt;
|-&lt;br /&gt;
|Codeine: PO&lt;br /&gt;
|100 mg&lt;br /&gt;
|-&lt;br /&gt;
|Diamorphine: IM, IV, SC&lt;br /&gt;
|3 mg&lt;br /&gt;
|-&lt;br /&gt;
|Dihydrocodeine: PO&lt;br /&gt;
|100 mg&lt;br /&gt;
|-&lt;br /&gt;
|Morphine: PO&lt;br /&gt;
|10 mg&lt;br /&gt;
|-&lt;br /&gt;
|Morphine: IM, IV, SC&lt;br /&gt;
|5 mg&lt;br /&gt;
|-&lt;br /&gt;
|Oxycodone: PO&lt;br /&gt;
|6.6 mg&lt;br /&gt;
|-&lt;br /&gt;
|Tramadol: PO&lt;br /&gt;
|100 mg&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Dosage==&lt;br /&gt;
&lt;br /&gt;
Morphine is usually administered as the sulphate. Doses are expressed as the salts. Dosage routes include the oral, subcutaneous, intramuscular, intravenous, intraspinal, and rectal routes. &lt;br /&gt;
&lt;br /&gt;
===For pain===&lt;br /&gt;
*Oral doses are usually equivalent to 5 to 20mg every 4 hours as syrup, or as immediate-release tablet. With modified-release preparations the 24-hour dose is usually given as a single dose or in 2 divided doses. With all modified-release preparations, additional doses of immediate-release tablet may be needed if breakthrough pain occurs. &lt;br /&gt;
*Rectally as suppositories in doses of 10 to 30mg every 4 hours.&lt;br /&gt;
*Subcutaneous or intramuscular injection is 10mg every 4 hours but may range from 5 to 20 mg.&lt;br /&gt;
&lt;br /&gt;
===For myocardial infarction===&lt;br /&gt;
Intravenous injection of 5 to 10 mg given at a rate of 1 to 2 mg/minute&lt;br /&gt;
&lt;br /&gt;
===Doses in children===&lt;br /&gt;
&lt;br /&gt;
The following initial doses are recommended by the BNFC according to age; doses should thereafter be adjusted according to response:&lt;br /&gt;
&lt;br /&gt;
By subcutaneous injection:&lt;br /&gt;
&lt;br /&gt;
*Neonates: 100 micrograms/kg every 6 hours&lt;br /&gt;
*1 to 5 months: 100 to 200 micrograms/kg every 6 hours&lt;br /&gt;
*6 months to 1 year: 100 to 200 micrograms/kg every 4 hours&lt;br /&gt;
*2 to 11 years: 200 micrograms/kg every 4 hours&lt;br /&gt;
*12 to 17 years: 2.5 to 10 mg every 4 hours&lt;br /&gt;
&lt;br /&gt;
By intravenous injection over at least 5 minutes:&lt;br /&gt;
*Neonates: 50 micrograms/kg every 6 hours&lt;br /&gt;
*1 to 5 months: 100 micrograms/kg every 6 hours &lt;br /&gt;
*6 months to 11 years: 100 micrograms/kg every 4 hours&lt;br /&gt;
*12 to 17 years: 5 mg every 4 hours&lt;br /&gt;
&lt;br /&gt;
By mouth or rectum:&lt;br /&gt;
*1 to 2 months: 50 to 100 micrograms/kg every 4 hours&lt;br /&gt;
*3 to 5 months: 100 to 150 micrograms/kg every 4 hours&lt;br /&gt;
*6 to 11 months: 200 micrograms/kg every 4 hours&lt;br /&gt;
*1 to 11 years: 200 to 300 micrograms/kg every 4 hours&lt;br /&gt;
*12 to 17 years: 5 to 10 mg every 4 hours&lt;br /&gt;
&lt;br /&gt;
For severe chronic pain: 5-10 mg q4h, adjusted if needed.&lt;br /&gt;
&lt;br /&gt;
IV Child dose based on body weight. adjusted if needed.&lt;br /&gt;
&lt;br /&gt;
===Palliative care pain management dose=== &lt;br /&gt;
20-60 mg in divided dose depends on where the patients was on opioid before.&lt;br /&gt;
&lt;br /&gt;
==Side Effects==&lt;br /&gt;
&lt;br /&gt;
As for &#039;&#039;&#039;Opioid Analgesic &lt;br /&gt;
in general&lt;br /&gt;
&lt;br /&gt;
The commonest adverse effects are nausea, vomiting, constipation, drowsiness and confusion.&lt;br /&gt;
&lt;br /&gt;
Large doses of opioids produce respiratory depression and hypotension, with circulatory failure and deepening coma. Death may occur from respiratory failure. &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Treatment of Adverse Effects&lt;br /&gt;
&lt;br /&gt;
1.	Constipation can be treated with laxatives such as senna tables and lactulose.&lt;br /&gt;
&lt;br /&gt;
2.	Nausea and vomiting can be alleviated by metoclopramide.&lt;br /&gt;
&lt;br /&gt;
3.	Intensive supportive therapy may be required to correct respiratory failure and shock. Naloxone is used for &lt;br /&gt;
rapid reversal of the severe respiratory depression and coma. &lt;br /&gt;
&lt;br /&gt;
Euphoria, nausea and vomiting, respiratory depression, constipation and cough suppression.&lt;br /&gt;
&lt;br /&gt;
==Pharmacokinetics==&lt;br /&gt;
&lt;br /&gt;
{|class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Oral bioavailability&lt;br /&gt;
|Morphine salts are well absorbed from the gastrointestinal tract but have poor oral bioavailability since they undergo extensive first-pass metabolism in the liver and gut. &lt;br /&gt;
After subcutaneous or intramuscular injection morphine is readily absorbed into the blood. &lt;br /&gt;
|-&lt;br /&gt;
!Onset of action&lt;br /&gt;
|Morphine is distributed throughout the body but mainly in the kidneys, liver, lungs and spleen, with lower concentrations in the brain and muscles. Morphine crosses the blood-brain barrier less readily than more lipid-soluble opioids such as diamorphine. Morphine diffuses across the placenta and also appear in breast milk and sweat. &lt;br /&gt;
|-&lt;br /&gt;
!Metabolism&lt;br /&gt;
|Up to 10% of a dose of morphine may be excreted into the faeces. The remainder is excreted in the urine.&lt;br /&gt;
|-&lt;br /&gt;
!Elimination half-life&lt;br /&gt;
|About 35% is protein bound. Mean plasma elimination half-life is about 2 hours. &lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
==Drug Management==&lt;br /&gt;
&lt;br /&gt;
===Efficiency=== &lt;br /&gt;
Relief of moderate to severe pain, especially that associated with cancer, myocardial infarction and surgery. &lt;br /&gt;
&lt;br /&gt;
===Contraindication=== &lt;br /&gt;
*acute respiratory depression and obstructive airways disease&lt;br /&gt;
*acute alcoholism&lt;br /&gt;
*convulsive disorders&lt;br /&gt;
*head injuries&lt;br /&gt;
*avoid in patients at risk of paralytic ileus&lt;br /&gt;
*patients with hypothyroidism&lt;br /&gt;
*patients with adrenocortical insufficiency&lt;br /&gt;
*renal or hepatic impairment&lt;br /&gt;
*prostatic hyperplasia&lt;br /&gt;
&lt;br /&gt;
Drowsiness may affect the ability to perform skilled tasks; those so affected should not drive or operate machinery.&lt;br /&gt;
&lt;br /&gt;
Morphine should be stopped gradually in patients who may have developed physical dependence, to avoid precipitating withdrawal symptoms (see &#039;&#039;&#039;Dependence and Withdrawal&#039;&#039;&#039;).&lt;br /&gt;
&lt;br /&gt;
Abrupt withdrawal of opioids precipitates a withdrawal syndrome. With morphine and diamorphine, withdrawal symptoms usually begin within a few hours, reach a peak within 36 to 72 hours, and then gradually subside; they develop more slowly with methadone.&lt;br /&gt;
&lt;br /&gt;
===Withdrawal symptom=== &lt;br /&gt;
Withdrawal symptoms include yawning, mydriasis, rhinorrhea, sneezing, muscle tremor, weakness, sweating, nausea vomiting, diarrhea, bone pain, abdominal and muscle cramps, increases in heart rate, respiratory rate, blood pressure and temperature.&lt;br /&gt;
&lt;br /&gt;
== FAQ ==&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
Follow the doctor&#039;s prescription, &lt;br /&gt;
Take with or without food&lt;br /&gt;
Take the medication with plenty of water&lt;br /&gt;
Can be crushed&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid abrupt withdrawal&lt;br /&gt;
=== What happen if I overdose? ===&lt;br /&gt;
Emergency situation, called 999 immediately&lt;br /&gt;
Antidote: Naloxone&lt;br /&gt;
=== What happen if I miss a dose? ===&lt;br /&gt;
Take it as soon as you remember. If it is near the time of the next dose, skip the missed dose. Take  &lt;br /&gt;
your next dose at the regular time. Do not double the dose to catch up.&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Thiamine&amp;diff=718</id>
		<title>Thiamine</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Thiamine&amp;diff=718"/>
		<updated>2020-09-28T13:16:24Z</updated>

		<summary type="html">&lt;p&gt;Annayung: Undo revision 717 by Annayung (talk)&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
==Pronunciation==&lt;br /&gt;
===Thiamine vitamin B1-50mg===&lt;br /&gt;
[[File:Thiamine vitamin B1-50mg.mp3]]&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Thiamine&amp;diff=717</id>
		<title>Thiamine</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Thiamine&amp;diff=717"/>
		<updated>2020-09-28T13:15:46Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
==Pronunciation==&lt;br /&gt;
===Thiamine vitamin B1-50mg===&lt;br /&gt;
[[File:Thiamine vitamin B1-50mg.mp3]]&lt;br /&gt;
&lt;br /&gt;
Hello world&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=716</id>
		<title>Fludrocortisone</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=716"/>
		<updated>2020-09-28T13:10:07Z</updated>

		<summary type="html">&lt;p&gt;Annayung: /* Introduction */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]] [[Category: Steroids]]&lt;br /&gt;
&#039;&#039;&#039;Fludrocortisone&#039;&#039;&#039; is a steroid with potent mineralocorticoid activity. &lt;br /&gt;
It is used to treat:&lt;br /&gt;
*Adrenocortical insufficiency&lt;br /&gt;
*Postural hypotension&lt;br /&gt;
*Adrenogenital syndrome&lt;br /&gt;
&lt;br /&gt;
== Introduction ==&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Generic Name&lt;br /&gt;
!HA Code&lt;br /&gt;
!Legal Classification&lt;br /&gt;
|-&lt;br /&gt;
|Fludrocortisone Acetate Tablet 100mcg&lt;br /&gt;
|FLUD01&lt;br /&gt;
|P1S1S3&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Brand Name&lt;br /&gt;
!HK Reg Number&lt;br /&gt;
!Active Ingredients&lt;br /&gt;
|-&lt;br /&gt;
|FLORINEF TABLET 0.1mg&lt;br /&gt;
|HK-00036&lt;br /&gt;
|fludrocortisone acetate&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Pronunciation ==&lt;br /&gt;
=== Fludrocortisone 100mcg ===&lt;br /&gt;
[[File:Fludrocortisone 100mcg.mp3]]&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Fludrocortisone is a corticosteroid with glucocorticoid and highly potent mineralocorticoid activity.&lt;br /&gt;
&lt;br /&gt;
== Dosage ==&lt;br /&gt;
Fludrocortisone is used, usually with hydrocortisone, for replacement therapy in adrenocortical insufficiency. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Replacement therapy in adrenal insufficiency&lt;br /&gt;
| Oral: 50-300 micrograms daily &lt;br /&gt;
|-&lt;br /&gt;
! Severe orthostatic hypotension&lt;br /&gt;
| Oral: 50-300 micrograms daily&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
It is also used ear drops in concentration of 0.1%.&lt;br /&gt;
&lt;br /&gt;
== Side Effects ==&lt;br /&gt;
Fludrocortisone acetate has glucocorticoid actions about 10 times as potent as hydrocortisone and mineralocorticoid effects more than 100 times as potent. &lt;br /&gt;
Adverse effects are mainly those due to mineralocorticoid activity:&lt;br /&gt;
*Sodium and water retention&lt;br /&gt;
*Swelling due to fluid retention (oedema)&lt;br /&gt;
*Hypertension&lt;br /&gt;
*Increased excretion of potassium leading to hypokalaemia&lt;br /&gt;
*Heart failure may be induced in susceptible patients&lt;br /&gt;
Other side-effects include:&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Steroid-induced diabetes&lt;br /&gt;
| Raised blood sugar level&lt;br /&gt;
|-&lt;br /&gt;
!Osteoporosis, muscle wasting and weakness&lt;br /&gt;
| Particularly danger in the elderly, as it can result in osteoporotic fractures for example of the hip or vertebrae&lt;br /&gt;
|-&lt;br /&gt;
! Susceptibility to infection&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
!Disturbances of the gut&lt;br /&gt;
| Indigestion, peptic ulcer, distension of the abdomen&lt;br /&gt;
|-&lt;br /&gt;
!Suppression of growth in children&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
!Endocrine side effects&lt;br /&gt;
|Menstrual irregularities , hirsutism (increased hair growth), weight gain&lt;br /&gt;
|-&lt;br /&gt;
!Neuropsychiatric side effects&lt;br /&gt;
| Aggravation of schizophrenia, aggravation of epilepsy, insomnia, irritability, depression&lt;br /&gt;
|-&lt;br /&gt;
!Dermatological side effects&lt;br /&gt;
| Easy bruising, impaired wound healing, thinning of skin and stretch marks&lt;br /&gt;
|-&lt;br /&gt;
!Ophthalmic side effects&lt;br /&gt;
| Glaucoma, partial loss of vision due to opacity in the lens of the eye (cataracts)&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
Fludrocortisone is readily absorbed from the gastrointestinal tract. The plasma half-life is about 3.5 hours, but fludrocortisone has a more prolonged biological half-life of 18 to 36 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Management ==&lt;br /&gt;
===Monitoring=== &lt;br /&gt;
*Elderly (close supervision required particularly on long-term treatment)&lt;br /&gt;
*Frequent monitoring required if history of tuberculosis (or X-ray changes)&lt;br /&gt;
*Blood sugar level, blood pressure, mood change&lt;br /&gt;
*Monitoring of the fluid intake and output, and daily weight records may give early warning of fluid retention&lt;br /&gt;
*Sodium intake may need to be reduced and calcium and potassium supplements may be necessary&lt;br /&gt;
*Back pain may signify osteoporosis&lt;br /&gt;
*Plasma renin, sodium, and potassium is checked through blood tests to verify that the correct dosage is reached&lt;br /&gt;
&lt;br /&gt;
=== Drug interaction ===&lt;br /&gt;
Interactions do not generally apply to steroid used for topical action including inhalation, unless specified. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Drugs given with steroid &lt;br /&gt;
!Potential adverse drug interactions&lt;br /&gt;
|-&lt;br /&gt;
| NSAIDs&lt;br /&gt;
| Increased risk of gastro-intestinal bleeding&lt;br /&gt;
|-&lt;br /&gt;
| Rifampicin&lt;br /&gt;
| Accelerate metabolism of fludrocortisone so reduce its effects &lt;br /&gt;
|-&lt;br /&gt;
| Antidiabetics&lt;br /&gt;
| Antagonize hypoglycemic effect, so may need to increase antidiabetic dosage &lt;br /&gt;
|-&lt;br /&gt;
| Antiepileptics such as carbamazepine, phenobarbitone, phenytoin&lt;br /&gt;
| Accelerate metabolism of fludrocortisone so reduce its effects &lt;br /&gt;
|-&lt;br /&gt;
| Antifungal e.g. amphotericin&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Antiviral e.g ritonavir&lt;br /&gt;
| Increase plasma concentration of steroid – increased risk of adrenal suppression&lt;br /&gt;
|-&lt;br /&gt;
| Digoxin&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Diuretics e.g. frusemide, hydrochlorothiazide&lt;br /&gt;
| Antagonize diuretic effect; increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Oral contraceptive (oestrogens)&lt;br /&gt;
| Increase plasma concentration of steroid&lt;br /&gt;
|-&lt;br /&gt;
| Theophylline&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
=== Caution ===&lt;br /&gt;
*Osteoporosis (post-menopausal women at special risk)&lt;br /&gt;
*Recent myocardial infarction, congestive heart failure&lt;br /&gt;
*Glaucoma (including family history)&lt;br /&gt;
*Ocular herpes simplex – risk of corneal perforation&lt;br /&gt;
*Psychiatric disorders (particularly if history of steroid-induced psychosis)&lt;br /&gt;
*Epilepsy&lt;br /&gt;
*Peptic ulcer&lt;br /&gt;
*Hypothyroidism&lt;br /&gt;
*Ulcerative colitis&lt;br /&gt;
*Diverticulitis&lt;br /&gt;
*Thromboembolic disorders&lt;br /&gt;
&lt;br /&gt;
=== Contraindication ===&lt;br /&gt;
*Acute infections&lt;br /&gt;
*Patients with active or doubtfully quiescent tuberculosis&lt;br /&gt;
*Concurrent treatment live virus vaccines for at least 3 months afterwards&lt;br /&gt;
=== Hepatic impairment ===&lt;br /&gt;
When steroids are administered orally or parenterally, the plasma-drug concentration may be increased in patients with hepatic impairment. The patient should be monitored closely.&lt;br /&gt;
=== Renal impairment ===&lt;br /&gt;
Should be used with caution in patients with renal impairment. &lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
It is not yet clear if use of fludrocortisone during pregnancy is safe for the fetus.&lt;br /&gt;
&lt;br /&gt;
=== Note ===&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Prolonged use of steroid&lt;br /&gt;
! Advice to patient&lt;br /&gt;
|-&lt;br /&gt;
| Increase susceptibility to infection&lt;br /&gt;
| Avoid contact with people who have chickenpox, shingles, or measles.&lt;br /&gt;
|-&lt;br /&gt;
| Suppresses the endogenous secretion of corticotrophin by the anterior pituitary, resulting the adrenal cortex becomes atrophied. &lt;br /&gt;
If given for more than 3 weeks, treatment MUST be stopped gradually. &lt;br /&gt;
| Patient must mention the course of steroid when receiving treatment for intercurrent illnesses or going through trauma such as surgery.&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== FAQ ==&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
The tablet MUST be taken with or after food to help reduce GI side-effects.&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid abruptly discontinue the medication. &lt;br /&gt;
Should not be taken with NSAIDs. &lt;br /&gt;
=== What happen if I overdose? ===&lt;br /&gt;
Contact your primary care doctor.&lt;br /&gt;
If emergency situation, call 999&lt;br /&gt;
=== What happen if I miss a dose? ===&lt;br /&gt;
Take it as soon as you &lt;br /&gt;
remember. If it is near the time &lt;br /&gt;
of the next dose, skip the missed &lt;br /&gt;
dose. Take your next dose at the &lt;br /&gt;
regular time. Do not double the &lt;br /&gt;
dose to catch up.&lt;br /&gt;
IV, IM and IA: administered by professionals&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=431</id>
		<title>Fludrocortisone</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=431"/>
		<updated>2020-09-05T12:32:05Z</updated>

		<summary type="html">&lt;p&gt;Annayung: /* Introduction */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]] [[Category: Steroids]]&lt;br /&gt;
== Introduction ==&lt;br /&gt;
Fludrocortisone is a steroid with potent mineralocorticoid activity. &lt;br /&gt;
It is used to treat:&lt;br /&gt;
*Adrenocortical insufficiency&lt;br /&gt;
*Postural hypotension&lt;br /&gt;
*Adrenogenital syndrome&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Generic Name&lt;br /&gt;
!HA Code&lt;br /&gt;
!Legal Classification&lt;br /&gt;
|-&lt;br /&gt;
|Fludrocortisone Acetate Tablet 100mcg&lt;br /&gt;
|FLUD01&lt;br /&gt;
|P1S1S3&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Brand Name&lt;br /&gt;
!HK Reg Number&lt;br /&gt;
!Active Ingredients&lt;br /&gt;
|-&lt;br /&gt;
|FLORINEF TABLET 0.1mg&lt;br /&gt;
|HK-00036&lt;br /&gt;
|fludrocortisone acetate&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Fludrocortisone is a corticosteroid with glucocorticoid and highly potent mineralocorticoid activity.&lt;br /&gt;
&lt;br /&gt;
== Dosage ==&lt;br /&gt;
Fludrocortisone is used, usually with hydrocortisone, for replacement therapy in adrenocortical insufficiency. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Replacement therapy in adrenal insufficiency&lt;br /&gt;
| Oral: 50-300 micrograms daily &lt;br /&gt;
|-&lt;br /&gt;
! severe orthostatic hypotension&lt;br /&gt;
| Oral: 50-300 micrograms daily&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
It is also used ear drops in concentration of 0.1%.&lt;br /&gt;
== Side Effects ==&lt;br /&gt;
Fludrocortisone acetate has glucocorticoid actions about 10 times as potent as hydrocortisone and mineralocorticoid effects more than 100 times as potent. &lt;br /&gt;
Adverse effects are mainly those due to mineralocorticoid activity:&lt;br /&gt;
*Sodium and water retention&lt;br /&gt;
*Swelling due to fluid retention (oedema)&lt;br /&gt;
*Hypertension&lt;br /&gt;
*Increased excretion of potassium leading to hypokalaemia&lt;br /&gt;
*Heart failure may be induced in susceptible patients&lt;br /&gt;
Other side-effects include:&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!steroid-induced diabetes&lt;br /&gt;
| Raised blood sugar level&lt;br /&gt;
|-&lt;br /&gt;
!Osteoporosis, muscle wasting and weakness&lt;br /&gt;
| Particularly danger in the elderly, as it can result in osteoporotic fractures for example of the hip or vertebrae&lt;br /&gt;
|-&lt;br /&gt;
! Susceptibility to infection&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
! Disturbances of the gut&lt;br /&gt;
| Indigestion, peptic ulcer, distension of the abdomen&lt;br /&gt;
|-&lt;br /&gt;
!Suppression of growth in children&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
!Endocrine side effects&lt;br /&gt;
|Menstrual irregularities , hirsutism (increased hair growth), weight gain&lt;br /&gt;
|-&lt;br /&gt;
!Neuropsychiatric side effects&lt;br /&gt;
| Aggravation of schizophrenia, aggravation of epilepsy, insomnia, irritability, depression&lt;br /&gt;
|-&lt;br /&gt;
!Dermatological side effects&lt;br /&gt;
| Easy bruising, impaired wound healing, thinning of skin and stretch marks&lt;br /&gt;
|-&lt;br /&gt;
!Ophthalmic side effects&lt;br /&gt;
| Glaucoma, partial loss of vision due to opacity in the lens of the eye (cataracts)&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
Fludrocortisone is readily absorbed from the gastrointestinal tract. The plasma half-life is about 3.5 hours, but fludrocortisone has a more prolonged biological half-life of 18 to 36 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Management ==&lt;br /&gt;
===Monitoring=== &lt;br /&gt;
*Elderly (close supervision required particularly on long-term treatment)&lt;br /&gt;
*Frequent monitoring required if history of tuberculosis (or X-ray changes)&lt;br /&gt;
*Blood sugar level, blood pressure, mood change&lt;br /&gt;
*Monitoring of the fluid intake and output, and daily weight records may give early warning of fluid retention&lt;br /&gt;
*Sodium intake may need to be reduced and calcium and potassium supplements may be necessary&lt;br /&gt;
*Back pain may signify osteoporosis&lt;br /&gt;
*Plasma renin, sodium, and potassium is checked through blood tests to verify that the correct dosage is reached&lt;br /&gt;
&lt;br /&gt;
=== Drug interaction ===&lt;br /&gt;
Interactions do not generally apply to steroid used for topical action including inhalation, unless specified. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Drugs given with steroid &lt;br /&gt;
!Potential adverse drug interactions&lt;br /&gt;
|-&lt;br /&gt;
| NSAIDs&lt;br /&gt;
| Increased risk of gastro-intestinal bleeding&lt;br /&gt;
|-&lt;br /&gt;
| Rifampicin&lt;br /&gt;
| Accelerate metabolism of fludrocortisone so reduce its effects &lt;br /&gt;
|-&lt;br /&gt;
| Antidiabetics&lt;br /&gt;
| Antagonize hypoglycemic effect, so may need to increase antidiabetic dosage &lt;br /&gt;
|-&lt;br /&gt;
| Antiepileptics such as carbamazepine, phenobarbitone, phenytoin&lt;br /&gt;
| Accelerate metabolism of fludrocortisone so reduce its effects &lt;br /&gt;
|-&lt;br /&gt;
| Antifungal e.g. amphotericin&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Antiviral e.g ritonavir&lt;br /&gt;
| Increase plasma concentration of steroid – increased risk of adrenal suppression&lt;br /&gt;
|-&lt;br /&gt;
| Digoxin&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Diuretics e.g. frusemide, hydrochlorothiazide&lt;br /&gt;
| Antagonize diuretic effect; increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Oral contraceptive (oestrogens)&lt;br /&gt;
| Increase plasma concentration of steroid&lt;br /&gt;
|-&lt;br /&gt;
| Theophylline&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
=== Caution ===&lt;br /&gt;
*Osteoporosis (post-menopausal women at special risk)&lt;br /&gt;
*Recent myocardial infarction, congestive heart failure&lt;br /&gt;
*Glaucoma (including family history)&lt;br /&gt;
*Ocular herpes simplex – risk of corneal perforation&lt;br /&gt;
*Psychiatric disorders (particularly if history of steroid-induced psychosis)&lt;br /&gt;
*Epilepsy&lt;br /&gt;
*Peptic ulcer&lt;br /&gt;
*Hypothyroidism&lt;br /&gt;
*Ulcerative colitis&lt;br /&gt;
*Diverticulitis&lt;br /&gt;
*Thromboembolic disorders&lt;br /&gt;
&lt;br /&gt;
=== Contraindication ===&lt;br /&gt;
*Acute infections&lt;br /&gt;
*Patients with active or doubtfully quiescent tuberculosis&lt;br /&gt;
*Concurrent treatment live virus vaccines for at least 3 months afterwards&lt;br /&gt;
=== Hepatic impairment ===&lt;br /&gt;
When steroids are administered orally or parenterally, the plasma-drug concentration may be increased in patients with hepatic impairment. The patient should be monitored closely.&lt;br /&gt;
=== Renal impairment ===&lt;br /&gt;
Should be used with caution in patients with renal impairment. &lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
It is not yet clear if use of fludrocortisone during pregnancy is safe for the fetus.&lt;br /&gt;
&lt;br /&gt;
=== Note ===&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Prolonged use of steroid&lt;br /&gt;
! Advice to patient&lt;br /&gt;
|-&lt;br /&gt;
| Increase susceptibility to infection&lt;br /&gt;
| Avoid contact with people who have chickenpox, shingles, or measles.&lt;br /&gt;
|-&lt;br /&gt;
| Suppresses the endogenous secretion of corticotrophin by the anterior pituitary, resulting the adrenal cortex becomes atrophied. &lt;br /&gt;
If given for more than 3 weeks, treatment MUST be stopped gradually. &lt;br /&gt;
| Patient must mention the course of steroid when receiving treatment for intercurrent illnesses or going through trauma such as surgery.&lt;br /&gt;
|}&lt;br /&gt;
== FAQ ==&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
The tablet MUST be taken with or after food to help reduce GI side-effects.&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid abruptly discontinue the medication. &lt;br /&gt;
Should not be taken with NSAIDs. &lt;br /&gt;
=== What happen if I overdose? ===&lt;br /&gt;
Contact your primary care doctor.&lt;br /&gt;
If emergency situation, call 999&lt;br /&gt;
=== What happen if I miss a dose? ===&lt;br /&gt;
Take it as soon as you &lt;br /&gt;
remember. If it is near the time &lt;br /&gt;
of the next dose, skip the missed &lt;br /&gt;
dose. Take your next dose at the &lt;br /&gt;
regular time. Do not double the &lt;br /&gt;
dose to catch up.&lt;br /&gt;
IV, IM and IA: administered by professionals&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=430</id>
		<title>Fludrocortisone</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=430"/>
		<updated>2020-09-05T12:30:57Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]] [[Category: Steroids]]&lt;br /&gt;
== Introduction ==&lt;br /&gt;
Fludrocortisone is a steroid with potent mineralocorticoid activity. &lt;br /&gt;
It is used to treat:&lt;br /&gt;
*Adrenocortical insufficiency&lt;br /&gt;
*Postural hypotension&lt;br /&gt;
*Adrenogenital syndrome&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Generic Name&lt;br /&gt;
!HA Code&lt;br /&gt;
!Legal Classification&lt;br /&gt;
|-&lt;br /&gt;
|Fludrocortisone Acetate Tablet 100mcg&lt;br /&gt;
|FLUD01&lt;br /&gt;
|P1S1S3&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Brand Name&lt;br /&gt;
!HK Reg Number&lt;br /&gt;
!Active Ingredients&lt;br /&gt;
|-&lt;br /&gt;
|FLORINEF TABLET 0.1mg&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|HK-00036&lt;br /&gt;
|fludrocortisone acetate&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Fludrocortisone is a corticosteroid with glucocorticoid and highly potent mineralocorticoid activity.&lt;br /&gt;
&lt;br /&gt;
== Dosage ==&lt;br /&gt;
Fludrocortisone is used, usually with hydrocortisone, for replacement therapy in adrenocortical insufficiency. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Replacement therapy in adrenal insufficiency&lt;br /&gt;
| Oral: 50-300 micrograms daily &lt;br /&gt;
|-&lt;br /&gt;
! severe orthostatic hypotension&lt;br /&gt;
| Oral: 50-300 micrograms daily&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
It is also used ear drops in concentration of 0.1%.&lt;br /&gt;
== Side Effects ==&lt;br /&gt;
Fludrocortisone acetate has glucocorticoid actions about 10 times as potent as hydrocortisone and mineralocorticoid effects more than 100 times as potent. &lt;br /&gt;
Adverse effects are mainly those due to mineralocorticoid activity:&lt;br /&gt;
*Sodium and water retention&lt;br /&gt;
*Swelling due to fluid retention (oedema)&lt;br /&gt;
*Hypertension&lt;br /&gt;
*Increased excretion of potassium leading to hypokalaemia&lt;br /&gt;
*Heart failure may be induced in susceptible patients&lt;br /&gt;
Other side-effects include:&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!steroid-induced diabetes&lt;br /&gt;
| Raised blood sugar level&lt;br /&gt;
|-&lt;br /&gt;
!Osteoporosis, muscle wasting and weakness&lt;br /&gt;
| Particularly danger in the elderly, as it can result in osteoporotic fractures for example of the hip or vertebrae&lt;br /&gt;
|-&lt;br /&gt;
! Susceptibility to infection&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
! Disturbances of the gut&lt;br /&gt;
| Indigestion, peptic ulcer, distension of the abdomen&lt;br /&gt;
|-&lt;br /&gt;
!Suppression of growth in children&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
!Endocrine side effects&lt;br /&gt;
|Menstrual irregularities , hirsutism (increased hair growth), weight gain&lt;br /&gt;
|-&lt;br /&gt;
!Neuropsychiatric side effects&lt;br /&gt;
| Aggravation of schizophrenia, aggravation of epilepsy, insomnia, irritability, depression&lt;br /&gt;
|-&lt;br /&gt;
!Dermatological side effects&lt;br /&gt;
| Easy bruising, impaired wound healing, thinning of skin and stretch marks&lt;br /&gt;
|-&lt;br /&gt;
!Ophthalmic side effects&lt;br /&gt;
| Glaucoma, partial loss of vision due to opacity in the lens of the eye (cataracts)&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
Fludrocortisone is readily absorbed from the gastrointestinal tract. The plasma half-life is about 3.5 hours, but fludrocortisone has a more prolonged biological half-life of 18 to 36 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Management ==&lt;br /&gt;
===Monitoring=== &lt;br /&gt;
*Elderly (close supervision required particularly on long-term treatment)&lt;br /&gt;
*Frequent monitoring required if history of tuberculosis (or X-ray changes)&lt;br /&gt;
*Blood sugar level, blood pressure, mood change&lt;br /&gt;
*Monitoring of the fluid intake and output, and daily weight records may give early warning of fluid retention&lt;br /&gt;
*Sodium intake may need to be reduced and calcium and potassium supplements may be necessary&lt;br /&gt;
*Back pain may signify osteoporosis&lt;br /&gt;
*Plasma renin, sodium, and potassium is checked through blood tests to verify that the correct dosage is reached&lt;br /&gt;
&lt;br /&gt;
=== Drug interaction ===&lt;br /&gt;
Interactions do not generally apply to steroid used for topical action including inhalation, unless specified. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Drugs given with steroid &lt;br /&gt;
!Potential adverse drug interactions&lt;br /&gt;
|-&lt;br /&gt;
| NSAIDs&lt;br /&gt;
| Increased risk of gastro-intestinal bleeding&lt;br /&gt;
|-&lt;br /&gt;
| Rifampicin&lt;br /&gt;
| Accelerate metabolism of fludrocortisone so reduce its effects &lt;br /&gt;
|-&lt;br /&gt;
| Antidiabetics&lt;br /&gt;
| Antagonize hypoglycemic effect, so may need to increase antidiabetic dosage &lt;br /&gt;
|-&lt;br /&gt;
| Antiepileptics such as carbamazepine, phenobarbitone, phenytoin&lt;br /&gt;
| Accelerate metabolism of fludrocortisone so reduce its effects &lt;br /&gt;
|-&lt;br /&gt;
| Antifungal e.g. amphotericin&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Antiviral e.g ritonavir&lt;br /&gt;
| Increase plasma concentration of steroid – increased risk of adrenal suppression&lt;br /&gt;
|-&lt;br /&gt;
| Digoxin&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Diuretics e.g. frusemide, hydrochlorothiazide&lt;br /&gt;
| Antagonize diuretic effect; increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Oral contraceptive (oestrogens)&lt;br /&gt;
| Increase plasma concentration of steroid&lt;br /&gt;
|-&lt;br /&gt;
| Theophylline&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
=== Caution ===&lt;br /&gt;
*Osteoporosis (post-menopausal women at special risk)&lt;br /&gt;
*Recent myocardial infarction, congestive heart failure&lt;br /&gt;
*Glaucoma (including family history)&lt;br /&gt;
*Ocular herpes simplex – risk of corneal perforation&lt;br /&gt;
*Psychiatric disorders (particularly if history of steroid-induced psychosis)&lt;br /&gt;
*Epilepsy&lt;br /&gt;
*Peptic ulcer&lt;br /&gt;
*Hypothyroidism&lt;br /&gt;
*Ulcerative colitis&lt;br /&gt;
*Diverticulitis&lt;br /&gt;
*Thromboembolic disorders&lt;br /&gt;
&lt;br /&gt;
=== Contraindication ===&lt;br /&gt;
*Acute infections&lt;br /&gt;
*Patients with active or doubtfully quiescent tuberculosis&lt;br /&gt;
*Concurrent treatment live virus vaccines for at least 3 months afterwards&lt;br /&gt;
=== Hepatic impairment ===&lt;br /&gt;
When steroids are administered orally or parenterally, the plasma-drug concentration may be increased in patients with hepatic impairment. The patient should be monitored closely.&lt;br /&gt;
=== Renal impairment ===&lt;br /&gt;
Should be used with caution in patients with renal impairment. &lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
It is not yet clear if use of fludrocortisone during pregnancy is safe for the fetus.&lt;br /&gt;
&lt;br /&gt;
=== Note ===&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Prolonged use of steroid&lt;br /&gt;
! Advice to patient&lt;br /&gt;
|-&lt;br /&gt;
| Increase susceptibility to infection&lt;br /&gt;
| Avoid contact with people who have chickenpox, shingles, or measles.&lt;br /&gt;
|-&lt;br /&gt;
| Suppresses the endogenous secretion of corticotrophin by the anterior pituitary, resulting the adrenal cortex becomes atrophied. &lt;br /&gt;
If given for more than 3 weeks, treatment MUST be stopped gradually. &lt;br /&gt;
| Patient must mention the course of steroid when receiving treatment for intercurrent illnesses or going through trauma such as surgery.&lt;br /&gt;
|}&lt;br /&gt;
== FAQ ==&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
The tablet MUST be taken with or after food to help reduce GI side-effects.&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid abruptly discontinue the medication. &lt;br /&gt;
Should not be taken with NSAIDs. &lt;br /&gt;
=== What happen if I overdose? ===&lt;br /&gt;
Contact your primary care doctor.&lt;br /&gt;
If emergency situation, call 999&lt;br /&gt;
=== What happen if I miss a dose? ===&lt;br /&gt;
Take it as soon as you &lt;br /&gt;
remember. If it is near the time &lt;br /&gt;
of the next dose, skip the missed &lt;br /&gt;
dose. Take your next dose at the &lt;br /&gt;
regular time. Do not double the &lt;br /&gt;
dose to catch up.&lt;br /&gt;
IV, IM and IA: administered by professionals&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=429</id>
		<title>Fludrocortisone</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=429"/>
		<updated>2020-09-05T12:29:56Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]] [[Category: Steroids]]&lt;br /&gt;
== Introduction ==&lt;br /&gt;
Fludrocortisone is a steroid with potent mineralocorticoid activity. &lt;br /&gt;
It is used to treat:&lt;br /&gt;
*Adrenocortical insufficiency&lt;br /&gt;
*Postural hypotension&lt;br /&gt;
*Adrenogenital syndrome&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Generic Name&lt;br /&gt;
!HA Code&lt;br /&gt;
!Legal Classification&lt;br /&gt;
|-&lt;br /&gt;
|Fludrocortisone Acetate Tablet 100mcg&lt;br /&gt;
|FLUD01&lt;br /&gt;
|P1S1S3&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Brand Name&lt;br /&gt;
!HK Reg Number&lt;br /&gt;
!Active Ingredients&lt;br /&gt;
|-&lt;br /&gt;
|FLORINEF TABLET 0.1mg&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|HK-00036&lt;br /&gt;
|fludrocortisone acetate&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Fludrocortisone is a corticosteroid with glucocorticoid and highly potent mineralocorticoid activity.&lt;br /&gt;
&lt;br /&gt;
== Dosage ==&lt;br /&gt;
Fludrocortisone is used, usually with hydrocortisone, for replacement therapy in adrenocortical insufficiency. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Replacement therapy in adrenal insufficiency&lt;br /&gt;
| Oral: 50-300 micrograms daily &lt;br /&gt;
|-&lt;br /&gt;
! severe orthostatic hypotension&lt;br /&gt;
| Oral: 50-300 micrograms daily&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
It is also used ear drops in concentration of 0.1%.&lt;br /&gt;
== Side Effects ==&lt;br /&gt;
Fludrocortisone acetate has glucocorticoid actions about 10 times as potent as hydrocortisone and mineralocorticoid effects more than 100 times as potent. &lt;br /&gt;
Adverse effects are mainly those due to mineralocorticoid activity:&lt;br /&gt;
*Sodium and water retention&lt;br /&gt;
*Swelling due to fluid retention (oedema)&lt;br /&gt;
*Hhypertension&lt;br /&gt;
*Increased excretion of potassium leading to hypokalaemia&lt;br /&gt;
*Heart failure may be induced in susceptible patients&lt;br /&gt;
Other side-effects include:&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!steroid-induced diabetes&lt;br /&gt;
| Raised blood sugar level&lt;br /&gt;
|-&lt;br /&gt;
!Osteoporosis, muscle wasting and weakness&lt;br /&gt;
| Particularly danger in the elderly, as it can result in osteoporotic fractures for example of the hip or vertebrae&lt;br /&gt;
|-&lt;br /&gt;
! Susceptibility to infection&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
! Disturbances of the gut&lt;br /&gt;
| Indigestion, peptic ulcer, distension of the abdomen&lt;br /&gt;
|-&lt;br /&gt;
!Suppression of growth in children&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
!Endocrine side effects&lt;br /&gt;
|Menstrual irregularities , hirsutism (increased hair growth), weight gain&lt;br /&gt;
|-&lt;br /&gt;
!Neuropsychiatric side effects&lt;br /&gt;
| Aggravation of schizophrenia, aggravation of epilepsy, insomnia, irritability, depression&lt;br /&gt;
|-&lt;br /&gt;
!Dermatological side effects&lt;br /&gt;
| Easy bruising, impaired wound healing, thinning of skin and stretch marks&lt;br /&gt;
|-&lt;br /&gt;
!Ophthalmic side effects&lt;br /&gt;
| Glaucoma, partial loss of vision due to opacity in the lens of the eye (cataracts)&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
Fludrocortisone is readily absorbed from the gastrointestinal tract. The plasma half-life is about 3.5 hours, but fludrocortisone has a more prolonged biological half-life of 18 to 36 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Management ==&lt;br /&gt;
===Monitoring=== &lt;br /&gt;
*Elderly (close supervision required particularly on long-term treatment)&lt;br /&gt;
*Frequent monitoring required if history of tuberculosis (or X-ray changes)&lt;br /&gt;
*Blood sugar level, blood pressure, mood change&lt;br /&gt;
*Monitoring of the fluid intake and output, and daily weight records may give early warning of fluid retention&lt;br /&gt;
*Sodium intake may need to be reduced and calcium and potassium supplements may be necessary&lt;br /&gt;
*Back pain may signify osteoporosis&lt;br /&gt;
*Plasma renin, sodium, and potassium is checked through blood tests to verify that the correct dosage is reached&lt;br /&gt;
&lt;br /&gt;
=== Drug interaction ===&lt;br /&gt;
Interactions do not generally apply to steroid used for topical action including inhalation, unless specified. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Drugs given with steroid &lt;br /&gt;
!Potential adverse drug interactions&lt;br /&gt;
|-&lt;br /&gt;
| NSAIDs&lt;br /&gt;
| Increased risk of gastro-intestinal bleeding&lt;br /&gt;
|-&lt;br /&gt;
| Rifampicin&lt;br /&gt;
| Accelerate metabolism of fludrocortisone so reduce its effects &lt;br /&gt;
|-&lt;br /&gt;
| Antidiabetics&lt;br /&gt;
| Antagonize hypoglycemic effect, so may need to increase antidiabetic dosage &lt;br /&gt;
|-&lt;br /&gt;
| Antiepileptics such as carbamazepine, phenobarbitone, phenytoin&lt;br /&gt;
| Accelerate metabolism of fludrocortisone so reduce its effects &lt;br /&gt;
|-&lt;br /&gt;
| Antifungal e.g. amphotericin&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Antiviral e.g ritonavir&lt;br /&gt;
| Increase plasma concentration of steroid – increased risk of adrenal suppression&lt;br /&gt;
|-&lt;br /&gt;
| Digoxin&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Diuretics e.g. frusemide, hydrochlorothiazide&lt;br /&gt;
| Antagonize diuretic effect; increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Oral contraceptive (oestrogens)&lt;br /&gt;
| Increase plasma concentration of steroid&lt;br /&gt;
|-&lt;br /&gt;
| Theophylline&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
=== Caution ===&lt;br /&gt;
*Osteoporosis (post-menopausal women at special risk)&lt;br /&gt;
*Recent myocardial infarction, congestive heart failure&lt;br /&gt;
*Glaucoma (including family history)&lt;br /&gt;
*Ocular herpes simplex – risk of corneal perforation&lt;br /&gt;
*Psychiatric disorders (particularly if history of steroid-induced psychosis)&lt;br /&gt;
*Epilepsy&lt;br /&gt;
*Peptic ulcer&lt;br /&gt;
*Hypothyroidism&lt;br /&gt;
*Ulcerative colitis&lt;br /&gt;
*Diverticulitis&lt;br /&gt;
*Thromboembolic disorders&lt;br /&gt;
&lt;br /&gt;
=== Contraindication ===&lt;br /&gt;
*Acute infections&lt;br /&gt;
*Patients with active or doubtfully quiescent tuberculosis&lt;br /&gt;
*Concurrent treatment live virus vaccines for at least 3 months afterwards&lt;br /&gt;
=== Hepatic impairment ===&lt;br /&gt;
When steroids are administered orally or parenterally, the plasma-drug concentration may be increased in patients with hepatic impairment. The patient should be monitored closely.&lt;br /&gt;
=== Renal impairment ===&lt;br /&gt;
Should be used with caution in patients with renal impairment. &lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
It is not yet clear if use of fludrocortisone during pregnancy is safe for the fetus.&lt;br /&gt;
&lt;br /&gt;
=== Note ===&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Prolonged use of steroid&lt;br /&gt;
! Advice to patient&lt;br /&gt;
|-&lt;br /&gt;
| Increase susceptibility to infection&lt;br /&gt;
| Avoid contact with people who have chickenpox, shingles, or measles.&lt;br /&gt;
|-&lt;br /&gt;
| Suppresses the endogenous secretion of corticotrophin by the anterior pituitary, resulting the adrenal cortex becomes atrophied. &lt;br /&gt;
If given for more than 3 weeks, treatment MUST be stopped gradually. &lt;br /&gt;
| Patient must mention the course of steroid when receiving treatment for intercurrent illnesses or going through trauma such as surgery.&lt;br /&gt;
|}&lt;br /&gt;
== FAQ ==&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
The tablet MUST be taken with or after food to help reduce GI side-effects.&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid abruptly discontinue the medication. &lt;br /&gt;
Should not be taken with NSAIDs. &lt;br /&gt;
=== What happen if I overdose? ===&lt;br /&gt;
Contact your primary care doctor.&lt;br /&gt;
If emergency situation, call 999&lt;br /&gt;
=== What happen if I miss a dose? ===&lt;br /&gt;
Take it as soon as you &lt;br /&gt;
remember. If it is near the time &lt;br /&gt;
of the next dose, skip the missed &lt;br /&gt;
dose. Take your next dose at the &lt;br /&gt;
regular time. Do not double the &lt;br /&gt;
dose to catch up.&lt;br /&gt;
IV, IM and IA: administered by professionals&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=428</id>
		<title>Fludrocortisone</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=428"/>
		<updated>2020-09-05T12:29:06Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]] [[Category: Steroids]]&lt;br /&gt;
== Introduction ==&lt;br /&gt;
Fludrocortisone is a steroid with potent mineralocorticoid activity. &lt;br /&gt;
It is used to treat:&lt;br /&gt;
*Adrenocortical insufficiency&lt;br /&gt;
*Postural hypotension&lt;br /&gt;
*Adrenogenital syndrome&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Generic Name&lt;br /&gt;
!HA Code&lt;br /&gt;
!Legal Classification&lt;br /&gt;
|-&lt;br /&gt;
|Fludrocortisone Acetate Tablet 100mcg&lt;br /&gt;
|FLUD01&lt;br /&gt;
|P1S1S3&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Brand Name&lt;br /&gt;
!HK Reg Number&lt;br /&gt;
!Active Ingredients&lt;br /&gt;
|-&lt;br /&gt;
|FLORINEF TABLET 0.1mg&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|HK-00036&lt;br /&gt;
|fludrocortisone acetate&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Fludrocortisone is a corticosteroid with glucocorticoid and highly potent mineralocorticoid activity.&lt;br /&gt;
&lt;br /&gt;
== Dosage ==&lt;br /&gt;
Fludrocortisone is used, usually with hydrocortisone, for replacement therapy in adrenocortical insufficiency. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Replacement therapy in adrenal insufficiency&lt;br /&gt;
| Oral: 50-300 micrograms daily &lt;br /&gt;
|-&lt;br /&gt;
! severe orthostatic hypotension&lt;br /&gt;
| Oral: 50-300 micrograms daily&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
It is also used ear drops in concentration of 0.1%.&lt;br /&gt;
== Side Effects ==&lt;br /&gt;
Fludrocortisone acetate has glucocorticoid actions about 10 times as potent as hydrocortisone and mineralocorticoid effects more than 100 times as potent. &lt;br /&gt;
Adverse effects are mainly those due to mineralocorticoid activity:&lt;br /&gt;
*sodium and water retention&lt;br /&gt;
*swelling due to fluid retention (oedema)&lt;br /&gt;
*hypertension&lt;br /&gt;
*increased excretion of potassium leading to hypokalaemia&lt;br /&gt;
*heart failure may be induced in susceptible patients&lt;br /&gt;
Other side-effects include:&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!steroid-induced diabetes&lt;br /&gt;
| Raised blood sugar level&lt;br /&gt;
|-&lt;br /&gt;
!Osteoporosis, muscle wasting and weakness&lt;br /&gt;
| Particularly danger in the elderly, as it can result in osteoporotic fractures for example of the hip or vertebrae&lt;br /&gt;
|-&lt;br /&gt;
! Susceptibility to infection&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
! Disturbances of the gut&lt;br /&gt;
| Indigestion, peptic ulcer, distension of the abdomen&lt;br /&gt;
|-&lt;br /&gt;
!Suppression of growth in children&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
!Endocrine side effects&lt;br /&gt;
|Menstrual irregularities , hirsutism (increased hair growth), weight gain&lt;br /&gt;
|-&lt;br /&gt;
!Neuropsychiatric side effects&lt;br /&gt;
| Aggravation of schizophrenia, aggravation of epilepsy, insomnia, irritability, depression&lt;br /&gt;
|-&lt;br /&gt;
!Dermatological side effects&lt;br /&gt;
| Easy bruising, impaired wound healing, thinning of skin and stretch marks&lt;br /&gt;
|-&lt;br /&gt;
!Ophthalmic side effects&lt;br /&gt;
| Glaucoma, partial loss of vision due to opacity in the lens of the eye (cataracts)&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
Fludrocortisone is readily absorbed from the gastrointestinal tract. The plasma half-life is about 3.5 hours, but fludrocortisone has a more prolonged biological half-life of 18 to 36 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Management ==&lt;br /&gt;
===Monitoring=== &lt;br /&gt;
*Elderly (close supervision required particularly on long-term treatment)&lt;br /&gt;
*Frequent monitoring required if history of tuberculosis (or X-ray changes)&lt;br /&gt;
*Blood sugar level, blood pressure, mood change&lt;br /&gt;
*Monitoring of the fluid intake and output, and daily weight records may give early warning of fluid retention&lt;br /&gt;
*Sodium intake may need to be reduced and calcium and potassium supplements may be necessary&lt;br /&gt;
*Back pain may signify osteoporosis&lt;br /&gt;
*Plasma renin, sodium, and potassium is checked through blood tests to verify that the correct dosage is reached&lt;br /&gt;
&lt;br /&gt;
=== Drug interaction ===&lt;br /&gt;
Interactions do not generally apply to steroid used for topical action including inhalation, unless specified. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Drugs given with steroid &lt;br /&gt;
!Potential adverse drug interactions&lt;br /&gt;
|-&lt;br /&gt;
| NSAIDs&lt;br /&gt;
| Increased risk of gastro-intestinal bleeding&lt;br /&gt;
|-&lt;br /&gt;
| Rifampicin&lt;br /&gt;
| Accelerate metabolism of fludrocortisone so reduce its effects &lt;br /&gt;
|-&lt;br /&gt;
| Antidiabetics&lt;br /&gt;
| Antagonize hypoglycemic effect, so may need to increase antidiabetic dosage &lt;br /&gt;
|-&lt;br /&gt;
| Antiepileptics such as carbamazepine, phenobarbitone, phenytoin&lt;br /&gt;
| Accelerate metabolism of fludrocortisone so reduce its effects &lt;br /&gt;
|-&lt;br /&gt;
| Antifungal e.g. amphotericin&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Antiviral e.g ritonavir&lt;br /&gt;
| Increase plasma concentration of steroid – increased risk of adrenal suppression&lt;br /&gt;
|-&lt;br /&gt;
| Digoxin&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Diuretics e.g. frusemide, hydrochlorothiazide&lt;br /&gt;
| Antagonize diuretic effect; increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Oral contraceptive (oestrogens)&lt;br /&gt;
| Increase plasma concentration of steroid&lt;br /&gt;
|-&lt;br /&gt;
| Theophylline&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
=== Caution ===&lt;br /&gt;
*Osteoporosis (post-menopausal women at special risk)&lt;br /&gt;
*Recent myocardial infarction, congestive heart failure&lt;br /&gt;
*Glaucoma (including family history)&lt;br /&gt;
*Ocular herpes simplex – risk of corneal perforation&lt;br /&gt;
*Psychiatric disorders (particularly if history of steroid-induced psychosis)&lt;br /&gt;
*Epilepsy&lt;br /&gt;
*Peptic ulcer&lt;br /&gt;
*Hypothyroidism&lt;br /&gt;
*Ulcerative colitis&lt;br /&gt;
*Diverticulitis&lt;br /&gt;
*Thromboembolic disorders&lt;br /&gt;
&lt;br /&gt;
=== Contraindication ===&lt;br /&gt;
*Acute infections&lt;br /&gt;
*Patients with active or doubtfully quiescent tuberculosis&lt;br /&gt;
*Concurrent treatment live virus vaccines for at least 3 months afterwards&lt;br /&gt;
=== Hepatic impairment ===&lt;br /&gt;
When steroids are administered orally or parenterally, the plasma-drug concentration may be increased in patients with hepatic impairment. The patient should be monitored closely.&lt;br /&gt;
=== Renal impairment ===&lt;br /&gt;
Should be used with caution in patients with renal impairment. &lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
It is not yet clear if use of fludrocortisone during pregnancy is safe for the fetus.&lt;br /&gt;
&lt;br /&gt;
=== Note ===&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Prolonged use of steroid&lt;br /&gt;
! Advice to patient&lt;br /&gt;
|-&lt;br /&gt;
| Increase susceptibility to infection&lt;br /&gt;
| Avoid contact with people who have chickenpox, shingles, or measles.&lt;br /&gt;
|-&lt;br /&gt;
| Suppresses the endogenous secretion of corticotrophin by the anterior pituitary, resulting the adrenal cortex becomes atrophied. &lt;br /&gt;
If given for more than 3 weeks, treatment MUST be stopped gradually. &lt;br /&gt;
| Patient must mention the course of steroid when receiving treatment for intercurrent illnesses or going through trauma such as surgery.&lt;br /&gt;
|}&lt;br /&gt;
== FAQ ==&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
The tablet MUST be taken with or after food to help reduce GI side-effects.&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid abruptly discontinue the medication. &lt;br /&gt;
Should not be taken with NSAIDs. &lt;br /&gt;
=== What happen if I overdose? ===&lt;br /&gt;
Contact your primary care doctor.&lt;br /&gt;
If emergency situation, call 999&lt;br /&gt;
=== What happen if I miss a dose? ===&lt;br /&gt;
Take it as soon as you &lt;br /&gt;
remember. If it is near the time &lt;br /&gt;
of the next dose, skip the missed &lt;br /&gt;
dose. Take your next dose at the &lt;br /&gt;
regular time. Do not double the &lt;br /&gt;
dose to catch up.&lt;br /&gt;
IV, IM and IA: administered by professionals&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Category:Steroids&amp;diff=427</id>
		<title>Category:Steroids</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Category:Steroids&amp;diff=427"/>
		<updated>2020-09-05T12:22:13Z</updated>

		<summary type="html">&lt;p&gt;Annayung: Created blank page&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=426</id>
		<title>Fludrocortisone</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=426"/>
		<updated>2020-09-05T12:21:49Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]] [[Category: Steroids]]&lt;br /&gt;
== Introduction ==&lt;br /&gt;
Fludrocortisone is a steroid with potent mineralocorticoid activity. &lt;br /&gt;
It is used to treat:&lt;br /&gt;
*adrenocortical insufficiency&lt;br /&gt;
*postural hypotension&lt;br /&gt;
*adrenogenital syndrome&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Generic Name&lt;br /&gt;
!HA Code&lt;br /&gt;
!Legal Classification&lt;br /&gt;
|-&lt;br /&gt;
|Fludrocortisone Acetate Tablet 100mcg&lt;br /&gt;
|FLUD01&lt;br /&gt;
|P1S1S3&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Brand Name&lt;br /&gt;
!HK Reg Number&lt;br /&gt;
!Active Ingredients&lt;br /&gt;
|-&lt;br /&gt;
|FLORINEF TABLET 0.1mg&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|HK-00036&lt;br /&gt;
|fludrocortisone acetate&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Fludrocortisone is a corticosteroid with glucocorticoid and highly potent mineralocorticoid activity.&lt;br /&gt;
&lt;br /&gt;
== Dosage ==&lt;br /&gt;
Fludrocortisone is used, usually with hydrocortisone, for replacement therapy in adrenocortical insufficiency. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Replacement therapy in adrenal insufficiency&lt;br /&gt;
| Oral: 50-300 micrograms daily &lt;br /&gt;
|-&lt;br /&gt;
! severe orthostatic hypotension&lt;br /&gt;
| Oral: 50-300 micrograms daily&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
It is also used ear drops in concentration of 0.1%.&lt;br /&gt;
== Side Effects ==&lt;br /&gt;
Fludrocortisone acetate has glucocorticoid actions about 10 times as potent as hydrocortisone and mineralocorticoid effects more than 100 times as potent. &lt;br /&gt;
Adverse effects are mainly those due to mineralocorticoid activity:&lt;br /&gt;
*sodium and water retention&lt;br /&gt;
*swelling due to fluid retention (oedema)&lt;br /&gt;
*hypertension&lt;br /&gt;
*increased excretion of potassium leading to hypokalaemia&lt;br /&gt;
*heart failure may be induced in susceptible patients&lt;br /&gt;
Other side-effects include:&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!steroid-induced diabetes&lt;br /&gt;
| Raised blood sugar level&lt;br /&gt;
|-&lt;br /&gt;
!Osteoporosis, muscle wasting and weakenss&lt;br /&gt;
| Is a danger, particularly in the elderly, as it can result in osteoporotic fractures for example of the hip or vertebrae&lt;br /&gt;
|-&lt;br /&gt;
! Susceptibility to infection&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
! Disturbances of the gut&lt;br /&gt;
| Indigestion, peptic ulcer, distension of the abdomen&lt;br /&gt;
|-&lt;br /&gt;
!Suppression of growth in children&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
!Endocrine side effects&lt;br /&gt;
|Menstrual irregularities , hirsutism (increased hair growth), weight gain&lt;br /&gt;
|-&lt;br /&gt;
!Neuropsychiatric side effects&lt;br /&gt;
| Aggravation of schizophrenia, aggravation of epilepsy, insomnia, irritability, depression&lt;br /&gt;
|-&lt;br /&gt;
!Dermatological side effects&lt;br /&gt;
| Easy bruising, impaired wound healing, thinning of skin and stretch marks&lt;br /&gt;
|-&lt;br /&gt;
!Ophthalmic side effects&lt;br /&gt;
| Glaucoma, partial loss of vision due to opacity in the lens of the eye (cataracts)&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
Fludrocortisone is readily absorbed from the gastrointestinal tract. The plasma half-life is about 3.5 hours, but fludrocortisone has a more prolonged biological half-life of 18 to 36 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Management ==&lt;br /&gt;
===Monitoring=== &lt;br /&gt;
*Elderly (close supervision required particularly on long-term treatment)&lt;br /&gt;
*Frequent monitoring required if history of tuberculosis (or X-ray changes)&lt;br /&gt;
*Blood sugar level, blood pressure, mood change&lt;br /&gt;
*Monitoring of the fluid intake and output, and daily weight records may give early warning of fluid retention&lt;br /&gt;
*Sodium intake may need to be reduced and calcium and potassium supplements may be necessary&lt;br /&gt;
*Back pain may signify osteoporosis&lt;br /&gt;
*Plasma renin, sodium, and potassium is checked through blood tests to verify that the correct dosage is reached&lt;br /&gt;
&lt;br /&gt;
=== Drug interaction ===&lt;br /&gt;
Interactions do not generally apply to steroid used for topical action including inhalation, unless specified. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Drugs given with steroid &lt;br /&gt;
!Potential adverse drug interactions&lt;br /&gt;
|-&lt;br /&gt;
| NSAIDs&lt;br /&gt;
| Increased risk of gastro-intestinal bleeding&lt;br /&gt;
|-&lt;br /&gt;
| Rifampicin&lt;br /&gt;
| Accelerate metabolism of fludrocortisone so reduce its effects &lt;br /&gt;
|-&lt;br /&gt;
| Antidiabetics&lt;br /&gt;
| Antagonize hypoglycemic effect, so may need to increase antidiabetic dosage &lt;br /&gt;
|-&lt;br /&gt;
| Antiepileptics such as carbamazepine, phenobarbitone, phenytoin&lt;br /&gt;
| Accelerate metabolism of fludrocortisone so reduce its effects &lt;br /&gt;
|-&lt;br /&gt;
| Antifungal e.g. amphotericin&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Antiviral e.g ritonavir&lt;br /&gt;
| Increase plasma concentration of steroid – increased risk of adrenal suppression&lt;br /&gt;
|-&lt;br /&gt;
| Digoxin&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Diuretics e.g. frusemide, hydrochlorothiazide&lt;br /&gt;
| Antagonize diuretic effect; increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Oral contraceptive (oestrogens)&lt;br /&gt;
| Increase plasma concentration of steroid&lt;br /&gt;
|-&lt;br /&gt;
| Theophylline&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
=== Caution ===&lt;br /&gt;
*Osteoporosis (post-menopausal women at special risk)&lt;br /&gt;
*Recent myocardial infarction, congestive heart failure&lt;br /&gt;
*Glaucoma (including family history)&lt;br /&gt;
*Ocular herpes simplex – risk of corneal perforation&lt;br /&gt;
*Psychiatric disorders (particularly if history of steroid-induced psychosis)&lt;br /&gt;
*Epilepsy&lt;br /&gt;
*Peptic ulcer&lt;br /&gt;
*Hypothyroidism&lt;br /&gt;
*Ulcerative colitis&lt;br /&gt;
*Diverticulitis&lt;br /&gt;
*Thromboembolic disorders&lt;br /&gt;
&lt;br /&gt;
=== Contraindication ===&lt;br /&gt;
*acute infections&lt;br /&gt;
*patients with active or doubtfully quiescent tuberculosis&lt;br /&gt;
*concurrent treatment live virus vaccines for at least 3 months afterwards&lt;br /&gt;
=== Hepatic impairment ===&lt;br /&gt;
When steroids are administered orally or parenterally, the plasma-drug concentration may be increased in patients with hepatic impairment. The patient should be monitored closely.&lt;br /&gt;
=== Renal impairment ===&lt;br /&gt;
Should be used with caution in patients with renal impairment. &lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
It is not yet clear if use of fludrocortisone during pregnancy is safe for the fetus.&lt;br /&gt;
&lt;br /&gt;
=== Note ===&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Prolonged use of steroid&lt;br /&gt;
! advice to patient&lt;br /&gt;
|-&lt;br /&gt;
| Increase susceptibility to infection&lt;br /&gt;
| Avoid contact with people who have chickenpox, shingles, or measles.&lt;br /&gt;
|-&lt;br /&gt;
| Suppresses the endogenous secretion of corticotrophin by the anterior pituitary, resulting the adrenal cortex becomes atrophied. &lt;br /&gt;
If given for more than 3 weeks, treatment MUST be stopped gradually. &lt;br /&gt;
| Patient must mention the course of steroid when receiving treatment for intercurrent illnesses or going through trauma such as surgery.&lt;br /&gt;
|}&lt;br /&gt;
== FAQ ==&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
The tablet MUST be taken with or after food to help reduce GI side-effects.&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid abruptly discontinue the medication. &lt;br /&gt;
Should not be taken with NSAIDs. &lt;br /&gt;
=== What happen if I overdose? ===&lt;br /&gt;
Contact your primary care doctor.&lt;br /&gt;
If emergency situation, call 999&lt;br /&gt;
=== What happen if I miss a dose? ===&lt;br /&gt;
Take it as soon as you &lt;br /&gt;
remember. If it is near the time &lt;br /&gt;
of the next dose, skip the missed &lt;br /&gt;
dose. Take your next dose at the &lt;br /&gt;
regular time. Do not double the &lt;br /&gt;
dose to catch up.&lt;br /&gt;
IV, IM and IA: administered by professionals&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=425</id>
		<title>Fludrocortisone</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=425"/>
		<updated>2020-09-05T12:18:23Z</updated>

		<summary type="html">&lt;p&gt;Annayung: /* Introduction */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
== Introduction ==&lt;br /&gt;
Fludrocortisone is a steroid with potent mineralocorticoid activity. &lt;br /&gt;
It is used to treat:&lt;br /&gt;
*adrenocortical insufficiency&lt;br /&gt;
*postural hypotension&lt;br /&gt;
*adrenogenital syndrome&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Generic Name&lt;br /&gt;
!HA Code&lt;br /&gt;
!Legal Classification&lt;br /&gt;
|-&lt;br /&gt;
|Fludrocortisone Acetate Tablet 100mcg&lt;br /&gt;
|FLUD01&lt;br /&gt;
|P1S1S3&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Brand Name&lt;br /&gt;
!HK Reg Number&lt;br /&gt;
!Active Ingredients&lt;br /&gt;
|-&lt;br /&gt;
|FLORINEF TABLET 0.1mg&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|HK-00036&lt;br /&gt;
|fludrocortisone acetate&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Fludrocortisone is a corticosteroid with glucocorticoid and highly potent mineralocorticoid activity.&lt;br /&gt;
&lt;br /&gt;
== Dosage ==&lt;br /&gt;
Fludrocortisone is used, usually with hydrocortisone, for replacement therapy in adrenocortical insufficiency. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Replacement therapy in adrenal insufficiency&lt;br /&gt;
| Oral: 50-300 micrograms daily &lt;br /&gt;
|-&lt;br /&gt;
! severe orthostatic hypotension&lt;br /&gt;
| Oral: 50-300 micrograms daily&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
It is also used ear drops in concentration of 0.1%.&lt;br /&gt;
== Side Effects ==&lt;br /&gt;
Fludrocortisone acetate has glucocorticoid actions about 10 times as potent as hydrocortisone and mineralocorticoid effects more than 100 times as potent. &lt;br /&gt;
Adverse effects are mainly those due to mineralocorticoid activity:&lt;br /&gt;
*sodium and water retention&lt;br /&gt;
*swelling due to fluid retention (oedema)&lt;br /&gt;
*hypertension&lt;br /&gt;
*increased excretion of potassium leading to hypokalaemia&lt;br /&gt;
*heart failure may be induced in susceptible patients&lt;br /&gt;
Other side-effects include:&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!steroid-induced diabetes&lt;br /&gt;
| Raised blood sugar level&lt;br /&gt;
|-&lt;br /&gt;
!Osteoporosis, muscle wasting and weakenss&lt;br /&gt;
| Is a danger, particularly in the elderly, as it can result in osteoporotic fractures for example of the hip or vertebrae&lt;br /&gt;
|-&lt;br /&gt;
! Susceptibility to infection&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
! Disturbances of the gut&lt;br /&gt;
| Indigestion, peptic ulcer, distension of the abdomen&lt;br /&gt;
|-&lt;br /&gt;
!Suppression of growth in children&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
!Endocrine side effects&lt;br /&gt;
|Menstrual irregularities , hirsutism (increased hair growth), weight gain&lt;br /&gt;
|-&lt;br /&gt;
!Neuropsychiatric side effects&lt;br /&gt;
| Aggravation of schizophrenia, aggravation of epilepsy, insomnia, irritability, depression&lt;br /&gt;
|-&lt;br /&gt;
!Dermatological side effects&lt;br /&gt;
| Easy bruising, impaired wound healing, thinning of skin and stretch marks&lt;br /&gt;
|-&lt;br /&gt;
!Ophthalmic side effects&lt;br /&gt;
| Glaucoma, partial loss of vision due to opacity in the lens of the eye (cataracts)&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
Fludrocortisone is readily absorbed from the gastrointestinal tract. The plasma half-life is about 3.5 hours, but fludrocortisone has a more prolonged biological half-life of 18 to 36 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Management ==&lt;br /&gt;
===Monitoring=== &lt;br /&gt;
*Elderly (close supervision required particularly on long-term treatment)&lt;br /&gt;
*Frequent monitoring required if history of tuberculosis (or X-ray changes)&lt;br /&gt;
*Blood sugar level, blood pressure, mood change&lt;br /&gt;
*Monitoring of the fluid intake and output, and daily weight records may give early warning of fluid retention&lt;br /&gt;
*Sodium intake may need to be reduced and calcium and potassium supplements may be necessary&lt;br /&gt;
*Back pain may signify osteoporosis&lt;br /&gt;
*Plasma renin, sodium, and potassium is checked through blood tests to verify that the correct dosage is reached&lt;br /&gt;
&lt;br /&gt;
=== Drug interaction ===&lt;br /&gt;
Interactions do not generally apply to steroid used for topical action including inhalation, unless specified. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Drugs given with steroid &lt;br /&gt;
!Potential adverse drug interactions&lt;br /&gt;
|-&lt;br /&gt;
| NSAIDs&lt;br /&gt;
| Increased risk of gastro-intestinal bleeding&lt;br /&gt;
|-&lt;br /&gt;
| Rifampicin&lt;br /&gt;
| Accelerate metabolism of fludrocortisone so reduce its effects &lt;br /&gt;
|-&lt;br /&gt;
| Antidiabetics&lt;br /&gt;
| Antagonize hypoglycemic effect, so may need to increase antidiabetic dosage &lt;br /&gt;
|-&lt;br /&gt;
| Antiepileptics such as carbamazepine, phenobarbitone, phenytoin&lt;br /&gt;
| Accelerate metabolism of fludrocortisone so reduce its effects &lt;br /&gt;
|-&lt;br /&gt;
| Antifungal e.g. amphotericin&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Antiviral e.g ritonavir&lt;br /&gt;
| Increase plasma concentration of steroid – increased risk of adrenal suppression&lt;br /&gt;
|-&lt;br /&gt;
| Digoxin&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Diuretics e.g. frusemide, hydrochlorothiazide&lt;br /&gt;
| Antagonize diuretic effect; increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Oral contraceptive (oestrogens)&lt;br /&gt;
| Increase plasma concentration of steroid&lt;br /&gt;
|-&lt;br /&gt;
| Theophylline&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
=== Caution ===&lt;br /&gt;
*Osteoporosis (post-menopausal women at special risk)&lt;br /&gt;
*Recent myocardial infarction, congestive heart failure&lt;br /&gt;
*Glaucoma (including family history)&lt;br /&gt;
*Ocular herpes simplex – risk of corneal perforation&lt;br /&gt;
*Psychiatric disorders (particularly if history of steroid-induced psychosis)&lt;br /&gt;
*Epilepsy&lt;br /&gt;
*Peptic ulcer&lt;br /&gt;
*Hypothyroidism&lt;br /&gt;
*Ulcerative colitis&lt;br /&gt;
*Diverticulitis&lt;br /&gt;
*Thromboembolic disorders&lt;br /&gt;
&lt;br /&gt;
=== Contraindication ===&lt;br /&gt;
*acute infections&lt;br /&gt;
*patients with active or doubtfully quiescent tuberculosis&lt;br /&gt;
*concurrent treatment live virus vaccines for at least 3 months afterwards&lt;br /&gt;
=== Hepatic impairment ===&lt;br /&gt;
When steroids are administered orally or parenterally, the plasma-drug concentration may be increased in patients with hepatic impairment. The patient should be monitored closely.&lt;br /&gt;
=== Renal impairment ===&lt;br /&gt;
Should be used with caution in patients with renal impairment. &lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
It is not yet clear if use of fludrocortisone during pregnancy is safe for the fetus.&lt;br /&gt;
&lt;br /&gt;
=== Note ===&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Prolonged use of steroid&lt;br /&gt;
! advice to patient&lt;br /&gt;
|-&lt;br /&gt;
| Increase susceptibility to infection&lt;br /&gt;
| Avoid contact with people who have chickenpox, shingles, or measles.&lt;br /&gt;
|-&lt;br /&gt;
| Suppresses the endogenous secretion of corticotrophin by the anterior pituitary, resulting the adrenal cortex becomes atrophied. &lt;br /&gt;
If given for more than 3 weeks, treatment MUST be stopped gradually. &lt;br /&gt;
| Patient must mention the course of steroid when receiving treatment for intercurrent illnesses or going through trauma such as surgery.&lt;br /&gt;
|}&lt;br /&gt;
== FAQ ==&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
The tablet MUST be taken with or after food to help reduce GI side-effects.&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid abruptly discontinue the medication. &lt;br /&gt;
Should not be taken with NSAIDs. &lt;br /&gt;
=== What happen if I overdose? ===&lt;br /&gt;
Contact your primary care doctor.&lt;br /&gt;
If emergency situation, call 999&lt;br /&gt;
=== What happen if I miss a dose? ===&lt;br /&gt;
Take it as soon as you &lt;br /&gt;
remember. If it is near the time &lt;br /&gt;
of the next dose, skip the missed &lt;br /&gt;
dose. Take your next dose at the &lt;br /&gt;
regular time. Do not double the &lt;br /&gt;
dose to catch up.&lt;br /&gt;
IV, IM and IA: administered by professionals&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=424</id>
		<title>Fludrocortisone</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=424"/>
		<updated>2020-09-05T12:18:00Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
== Introduction ==&lt;br /&gt;
[[File:Trifluoperazine 1mg.mp3]]&lt;br /&gt;
Fludrocortisone is a steroid with potent mineralocorticoid activity. &lt;br /&gt;
It is used to treat:&lt;br /&gt;
*adrenocortical insufficiency&lt;br /&gt;
*postural hypotension&lt;br /&gt;
*adrenogenital syndrome&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Generic Name&lt;br /&gt;
!HA Code&lt;br /&gt;
!Legal Classification&lt;br /&gt;
|-&lt;br /&gt;
|Fludrocortisone Acetate Tablet 100mcg&lt;br /&gt;
|FLUD01&lt;br /&gt;
|P1S1S3&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Brand Name&lt;br /&gt;
!HK Reg Number&lt;br /&gt;
!Active Ingredients&lt;br /&gt;
|-&lt;br /&gt;
|FLORINEF TABLET 0.1mg&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|HK-00036&lt;br /&gt;
|fludrocortisone acetate&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Fludrocortisone is a corticosteroid with glucocorticoid and highly potent mineralocorticoid activity.&lt;br /&gt;
&lt;br /&gt;
== Dosage ==&lt;br /&gt;
Fludrocortisone is used, usually with hydrocortisone, for replacement therapy in adrenocortical insufficiency. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Replacement therapy in adrenal insufficiency&lt;br /&gt;
| Oral: 50-300 micrograms daily &lt;br /&gt;
|-&lt;br /&gt;
! severe orthostatic hypotension&lt;br /&gt;
| Oral: 50-300 micrograms daily&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
It is also used ear drops in concentration of 0.1%.&lt;br /&gt;
== Side Effects ==&lt;br /&gt;
Fludrocortisone acetate has glucocorticoid actions about 10 times as potent as hydrocortisone and mineralocorticoid effects more than 100 times as potent. &lt;br /&gt;
Adverse effects are mainly those due to mineralocorticoid activity:&lt;br /&gt;
*sodium and water retention&lt;br /&gt;
*swelling due to fluid retention (oedema)&lt;br /&gt;
*hypertension&lt;br /&gt;
*increased excretion of potassium leading to hypokalaemia&lt;br /&gt;
*heart failure may be induced in susceptible patients&lt;br /&gt;
Other side-effects include:&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!steroid-induced diabetes&lt;br /&gt;
| Raised blood sugar level&lt;br /&gt;
|-&lt;br /&gt;
!Osteoporosis, muscle wasting and weakenss&lt;br /&gt;
| Is a danger, particularly in the elderly, as it can result in osteoporotic fractures for example of the hip or vertebrae&lt;br /&gt;
|-&lt;br /&gt;
! Susceptibility to infection&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
! Disturbances of the gut&lt;br /&gt;
| Indigestion, peptic ulcer, distension of the abdomen&lt;br /&gt;
|-&lt;br /&gt;
!Suppression of growth in children&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
!Endocrine side effects&lt;br /&gt;
|Menstrual irregularities , hirsutism (increased hair growth), weight gain&lt;br /&gt;
|-&lt;br /&gt;
!Neuropsychiatric side effects&lt;br /&gt;
| Aggravation of schizophrenia, aggravation of epilepsy, insomnia, irritability, depression&lt;br /&gt;
|-&lt;br /&gt;
!Dermatological side effects&lt;br /&gt;
| Easy bruising, impaired wound healing, thinning of skin and stretch marks&lt;br /&gt;
|-&lt;br /&gt;
!Ophthalmic side effects&lt;br /&gt;
| Glaucoma, partial loss of vision due to opacity in the lens of the eye (cataracts)&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
Fludrocortisone is readily absorbed from the gastrointestinal tract. The plasma half-life is about 3.5 hours, but fludrocortisone has a more prolonged biological half-life of 18 to 36 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Management ==&lt;br /&gt;
===Monitoring=== &lt;br /&gt;
*Elderly (close supervision required particularly on long-term treatment)&lt;br /&gt;
*Frequent monitoring required if history of tuberculosis (or X-ray changes)&lt;br /&gt;
*Blood sugar level, blood pressure, mood change&lt;br /&gt;
*Monitoring of the fluid intake and output, and daily weight records may give early warning of fluid retention&lt;br /&gt;
*Sodium intake may need to be reduced and calcium and potassium supplements may be necessary&lt;br /&gt;
*Back pain may signify osteoporosis&lt;br /&gt;
*Plasma renin, sodium, and potassium is checked through blood tests to verify that the correct dosage is reached&lt;br /&gt;
&lt;br /&gt;
=== Drug interaction ===&lt;br /&gt;
Interactions do not generally apply to steroid used for topical action including inhalation, unless specified. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Drugs given with steroid &lt;br /&gt;
!Potential adverse drug interactions&lt;br /&gt;
|-&lt;br /&gt;
| NSAIDs&lt;br /&gt;
| Increased risk of gastro-intestinal bleeding&lt;br /&gt;
|-&lt;br /&gt;
| Rifampicin&lt;br /&gt;
| Accelerate metabolism of fludrocortisone so reduce its effects &lt;br /&gt;
|-&lt;br /&gt;
| Antidiabetics&lt;br /&gt;
| Antagonize hypoglycemic effect, so may need to increase antidiabetic dosage &lt;br /&gt;
|-&lt;br /&gt;
| Antiepileptics such as carbamazepine, phenobarbitone, phenytoin&lt;br /&gt;
| Accelerate metabolism of fludrocortisone so reduce its effects &lt;br /&gt;
|-&lt;br /&gt;
| Antifungal e.g. amphotericin&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Antiviral e.g ritonavir&lt;br /&gt;
| Increase plasma concentration of steroid – increased risk of adrenal suppression&lt;br /&gt;
|-&lt;br /&gt;
| Digoxin&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Diuretics e.g. frusemide, hydrochlorothiazide&lt;br /&gt;
| Antagonize diuretic effect; increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Oral contraceptive (oestrogens)&lt;br /&gt;
| Increase plasma concentration of steroid&lt;br /&gt;
|-&lt;br /&gt;
| Theophylline&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
=== Caution ===&lt;br /&gt;
*Osteoporosis (post-menopausal women at special risk)&lt;br /&gt;
*Recent myocardial infarction, congestive heart failure&lt;br /&gt;
*Glaucoma (including family history)&lt;br /&gt;
*Ocular herpes simplex – risk of corneal perforation&lt;br /&gt;
*Psychiatric disorders (particularly if history of steroid-induced psychosis)&lt;br /&gt;
*Epilepsy&lt;br /&gt;
*Peptic ulcer&lt;br /&gt;
*Hypothyroidism&lt;br /&gt;
*Ulcerative colitis&lt;br /&gt;
*Diverticulitis&lt;br /&gt;
*Thromboembolic disorders&lt;br /&gt;
&lt;br /&gt;
=== Contraindication ===&lt;br /&gt;
*acute infections&lt;br /&gt;
*patients with active or doubtfully quiescent tuberculosis&lt;br /&gt;
*concurrent treatment live virus vaccines for at least 3 months afterwards&lt;br /&gt;
=== Hepatic impairment ===&lt;br /&gt;
When steroids are administered orally or parenterally, the plasma-drug concentration may be increased in patients with hepatic impairment. The patient should be monitored closely.&lt;br /&gt;
=== Renal impairment ===&lt;br /&gt;
Should be used with caution in patients with renal impairment. &lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
It is not yet clear if use of fludrocortisone during pregnancy is safe for the fetus.&lt;br /&gt;
&lt;br /&gt;
=== Note ===&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Prolonged use of steroid&lt;br /&gt;
! advice to patient&lt;br /&gt;
|-&lt;br /&gt;
| Increase susceptibility to infection&lt;br /&gt;
| Avoid contact with people who have chickenpox, shingles, or measles.&lt;br /&gt;
|-&lt;br /&gt;
| Suppresses the endogenous secretion of corticotrophin by the anterior pituitary, resulting the adrenal cortex becomes atrophied. &lt;br /&gt;
If given for more than 3 weeks, treatment MUST be stopped gradually. &lt;br /&gt;
| Patient must mention the course of steroid when receiving treatment for intercurrent illnesses or going through trauma such as surgery.&lt;br /&gt;
|}&lt;br /&gt;
== FAQ ==&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
The tablet MUST be taken with or after food to help reduce GI side-effects.&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid abruptly discontinue the medication. &lt;br /&gt;
Should not be taken with NSAIDs. &lt;br /&gt;
=== What happen if I overdose? ===&lt;br /&gt;
Contact your primary care doctor.&lt;br /&gt;
If emergency situation, call 999&lt;br /&gt;
=== What happen if I miss a dose? ===&lt;br /&gt;
Take it as soon as you &lt;br /&gt;
remember. If it is near the time &lt;br /&gt;
of the next dose, skip the missed &lt;br /&gt;
dose. Take your next dose at the &lt;br /&gt;
regular time. Do not double the &lt;br /&gt;
dose to catch up.&lt;br /&gt;
IV, IM and IA: administered by professionals&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Celecoxib&amp;diff=423</id>
		<title>Celecoxib</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Celecoxib&amp;diff=423"/>
		<updated>2020-09-05T12:16:42Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
== Introduction ==&lt;br /&gt;
&lt;br /&gt;
Celecoxib is a nonsteroidal anti-inflammatory drug, an NSAID, selectively inhibit cyclo-oxygenase-2 (COX-2). As an NSAID, celecoxib is an analgesic, anti-inflammatory and antipyretic.&lt;br /&gt;
&lt;br /&gt;
Clinical indications for indomethacin include:&lt;br /&gt;
&lt;br /&gt;
*rheumatoid arthritis&lt;br /&gt;
*alkylosing spondylitis&lt;br /&gt;
*osteoarthritis&lt;br /&gt;
*gouty arthritis&lt;br /&gt;
*acute painful shoulder bursitis or tendinitis&lt;br /&gt;
&lt;br /&gt;
It is also be used in menstrual pain, headaches, dental pain, postoperative and postpartum pain.&lt;br /&gt;
&lt;br /&gt;
== FAQ ==&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
Should always be taken with food. Nearly all patients benefit from an ulcer protective drug (e.g. antacids, or famotidine 20mg or omeprazole 20 mg at bedtime).&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
&lt;br /&gt;
*Anti-inflammatory agent&lt;br /&gt;
*Non-steroidal anti-inflammatory drug (NSAID)&lt;br /&gt;
*Highly selective COX-2 inhibitor&lt;br /&gt;
&lt;br /&gt;
== Dosage ==&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Osteoarthritis&lt;br /&gt;
| Oral: 200 mg daily given as a single dose or in 2 divided doses. If necessary a dose of 200 mg twice daily may be used.&lt;br /&gt;
|-&lt;br /&gt;
! Rheumatoid arthritis&lt;br /&gt;
| Oral: 100 to 200 mg given twice daily.&lt;br /&gt;
|-&lt;br /&gt;
! Ankylosing Spondylitis&lt;br /&gt;
| Oral: an initial dose of 200 mg daily, as a single or in 2 divided doses.&lt;br /&gt;
In the USA, the dose may be increased to 400 mg daily after 6 weeks, although if no response is seen at this dose a further 6 weeks, alternative treatments should be considered.&lt;br /&gt;
|-&lt;br /&gt;
! Pain and Dysmenorrhea&lt;br /&gt;
|Oral: an initial dose of 400 mg followed by an additional dose of 200 mg, if necessary, is recommended on the first day; thereafter the dose is 200mg twice daily.&lt;br /&gt;
In patients with hepatic impairment and in those also taking fluconazole, a potent inhibitor of the cytochrome P450 isoenzyme CYP2C9, the dose of celecoxib should be reduced to half the recommended dose. &lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
=== Administration in children ===&lt;br /&gt;
For the treatment of juvenile idiopathic arthritis in children aged 2 years and over, the recommended oral doses, based on body-weight, are:&lt;br /&gt;
*10 to 25 kg: 50 mg twice daily&lt;br /&gt;
*Over 25 kg: 100 mg twice daily&lt;br /&gt;
It is recommended that children who are deficient in the cytochrome P450 isoenzyme CYP2C9 and hence poor metabolizers of celecoxib should be given alternative treatment.&lt;br /&gt;
The contents of a celecoxib capsule may be sprinkled onto pureed meal if a patient has difficulty swallowing the capsules. The sprinkled capsule should be taken immediately; it remains stable at a temperature of between 2 degrees to 8 degrees for up to 6 hours.&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
Peak plasma concentrations occur after 3 hours of an oral dose. &lt;br /&gt;
Plasma protein binding is about 97%. Celecoxib is metabolized in the liver mainly by the cytochrome P450 isoenzyme CYP2C9. It is eliminated mainly as metabolites in the faeces and urine. &lt;br /&gt;
The plasma elimination half-life is about 11 hours.&lt;br /&gt;
Celecoxib is distributed into breast milk. &lt;br /&gt;
== Side Effects ==&lt;br /&gt;
Common side effects include:&lt;br /&gt;
*Abdominal pain, nausea and diarrhea.&lt;br /&gt;
Serious side effects may include:&lt;br /&gt;
*Heart attacks&lt;br /&gt;
*Strokes&lt;br /&gt;
*Gastrointestinal perforation&lt;br /&gt;
*Gastrointestinal bleeding&lt;br /&gt;
*Kidney failure&lt;br /&gt;
*anaphylaxis&lt;br /&gt;
It is generally accepted that COX-2 inhibitor may cause less gastrotoxicity than that seen with the non-selective inhibition of the traditional NSAIDs. However, reports that upper gastrointestinal perforation, ulceration and bleeds have occurred with celecoxib treatment and should not be used in patients with active gastrointestinal ulceration or bleeding.&lt;br /&gt;
&lt;br /&gt;
== Drug Management ==&lt;br /&gt;
===Monitoring=== &lt;br /&gt;
*Regular physical examination to detect edema and signs of central nervous side effects. &lt;br /&gt;
*Blood pressure checks will reveal development of hypertension. &lt;br /&gt;
*Periodic serum electrolyte (sodium, potassium, chloride) measurements, &lt;br /&gt;
*complete blood counts and &lt;br /&gt;
*assessment of liver enzymes as well as creatinine (renal function) should be performed. &lt;br /&gt;
This is particularly important if Indomethacin is given together with an ACE inhibitor or with potassium-sparing diuretic (e.g. spironolactone), because these combinations can lead to hyperkalemia and/or serious kidney failure.&lt;br /&gt;
&lt;br /&gt;
===Drug Interaction===  &lt;br /&gt;
*the metabolism of celecoxib is mediated by the cytochrome P450 isoenzyme CYP2C9. Use  of other drugs that inhibit or induce by this isoenzyme may result in changes in plasma concentration of celecoxib. Fluconazole has increased plasma concentrations of celecoxib and it is recommended that the dose of celecoxib should be halved when given with fluconazole.&lt;br /&gt;
*Increases the blood thinning effects of warfarin by displacing them from their plasma protein binding and increases their free concentrations in the bloodstream, so increases the risk of bleeding &lt;br /&gt;
*Increase the risk of adverse effects of lithium, methotrexate and cardiac glycosides by lowering their excretion via the kidneys.&lt;br /&gt;
*Increase risk of kidney failure if given with ACE inhibitors such as lisinopril, ciclosporin, tacrolimus and diuretics, such as hydrochlorothiazide.&lt;br /&gt;
*Increase risk of hyperkalaemia with ACE inhibitors and potassium-sparing diuretics such as spironolactone. &lt;br /&gt;
*Use of more than one NSAID together (including aspirin) should be avoided because of the increased risk of adverse effects.&lt;br /&gt;
*It adds to the risk of gastrointestinal bleeding and ulceration when used with steroids, the SSRIs (such as sertraline or fluoxetine), the SNRI venlafaxaine, the antiplatelet clopidogrel, bisphosphonates or pentoxifylline. &lt;br /&gt;
&lt;br /&gt;
Many NSAIDs, but particularly indomethacin, cause lithium retention by reducing its excretion by the kidney. Thus, indomethacin users have an elevated risk of lithium toxicity. For patients taking lithium (e.g. for treatment of bipolar disorder), less toxic NSAIDs such as sulindac is preferred.&lt;br /&gt;
All NSAIDs, including indomethacin, also increase plasma renin activity and aldosterone levels, and increase sodium and potassium retention. Vasopressin activity is also enhanced. Together these may lead to:&lt;br /&gt;
*Edema (swelling due to fluid retention)&lt;br /&gt;
*Hyperkaelemia (high potassium levels)&lt;br /&gt;
*Hypernatremia (high sodium levels)&lt;br /&gt;
*hypertension&lt;br /&gt;
&lt;br /&gt;
===Contraindication===&lt;br /&gt;
*Allergy to aspirin or other NSAIDs&lt;br /&gt;
*Avoided by patients with a history of asthma attacks&lt;br /&gt;
*Contraindicated during pregnancy and in lactating women.&lt;br /&gt;
*Active stomach and/or duodenal ulceration or gastrointestinal bleeding, or history of peptic ulcer disease&lt;br /&gt;
*Inflammatory bowel disease such as Crohn’s disease or ulcerative colitis&lt;br /&gt;
*Severe congestive heart failure (NYHA class II to IV)&lt;br /&gt;
*Severe chronic kidney disease (creatinine clearance &amp;lt;30 mi/min)&lt;br /&gt;
*Caution in patients with severe, active bleeding such as cerebral hemorrhage&lt;br /&gt;
*Caution in patients with fluid retention or heart failure&lt;br /&gt;
*Caution in patients with Parkinson’s disease, epilepsy, psychotic disorders (sulindac may worsen these conditions)&lt;br /&gt;
*Concurrent with potassium sparing diuretics&lt;br /&gt;
*Can lead to onset of new hypertension or worsening of pre-existing hypertension&lt;br /&gt;
*Avoid in pregnancy and in breast-feeding women&lt;br /&gt;
&lt;br /&gt;
===Note===&lt;br /&gt;
*Celecoxib should not be used after coronary artery bypass surgery as there may be an increased risk of adverse effects such as myocardial infarction and stroke.&lt;br /&gt;
*It should be used with caution, it at all, in patients with a history of ischaemic heart disease, peripheral arterial disease, or cerebrovascular disease.&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=422</id>
		<title>Fludrocortisone</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=422"/>
		<updated>2020-09-05T12:16:37Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
== Introduction ==&lt;br /&gt;
&lt;br /&gt;
Fludrocortisone is a steroid with potent mineralocorticoid activity. &lt;br /&gt;
It is used to treat:&lt;br /&gt;
*adrenocortical insufficiency&lt;br /&gt;
*postural hypotension&lt;br /&gt;
*adrenogenital syndrome&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Generic Name&lt;br /&gt;
!HA Code&lt;br /&gt;
!Legal Classification&lt;br /&gt;
|-&lt;br /&gt;
|Fludrocortisone Acetate Tablet 100mcg&lt;br /&gt;
|FLUD01&lt;br /&gt;
|P1S1S3&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Brand Name&lt;br /&gt;
!HK Reg Number&lt;br /&gt;
!Active Ingredients&lt;br /&gt;
|-&lt;br /&gt;
|FLORINEF TABLET 0.1mg&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|HK-00036&lt;br /&gt;
|fludrocortisone acetate&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Fludrocortisone is a corticosteroid with glucocorticoid and highly potent mineralocorticoid activity.&lt;br /&gt;
&lt;br /&gt;
== Dosage ==&lt;br /&gt;
Fludrocortisone is used, usually with hydrocortisone, for replacement therapy in adrenocortical insufficiency. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Replacement therapy in adrenal insufficiency&lt;br /&gt;
| Oral: 50-300 micrograms daily &lt;br /&gt;
|-&lt;br /&gt;
! severe orthostatic hypotension&lt;br /&gt;
| Oral: 50-300 micrograms daily&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
It is also used ear drops in concentration of 0.1%.&lt;br /&gt;
== Side Effects ==&lt;br /&gt;
Fludrocortisone acetate has glucocorticoid actions about 10 times as potent as hydrocortisone and mineralocorticoid effects more than 100 times as potent. &lt;br /&gt;
Adverse effects are mainly those due to mineralocorticoid activity:&lt;br /&gt;
*sodium and water retention&lt;br /&gt;
*swelling due to fluid retention (oedema)&lt;br /&gt;
*hypertension&lt;br /&gt;
*increased excretion of potassium leading to hypokalaemia&lt;br /&gt;
*heart failure may be induced in susceptible patients&lt;br /&gt;
Other side-effects include:&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!steroid-induced diabetes&lt;br /&gt;
| Raised blood sugar level&lt;br /&gt;
|-&lt;br /&gt;
!Osteoporosis, muscle wasting and weakenss&lt;br /&gt;
| Is a danger, particularly in the elderly, as it can result in osteoporotic fractures for example of the hip or vertebrae&lt;br /&gt;
|-&lt;br /&gt;
! Susceptibility to infection&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
! Disturbances of the gut&lt;br /&gt;
| Indigestion, peptic ulcer, distension of the abdomen&lt;br /&gt;
|-&lt;br /&gt;
!Suppression of growth in children&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
!Endocrine side effects&lt;br /&gt;
|Menstrual irregularities , hirsutism (increased hair growth), weight gain&lt;br /&gt;
|-&lt;br /&gt;
!Neuropsychiatric side effects&lt;br /&gt;
| Aggravation of schizophrenia, aggravation of epilepsy, insomnia, irritability, depression&lt;br /&gt;
|-&lt;br /&gt;
!Dermatological side effects&lt;br /&gt;
| Easy bruising, impaired wound healing, thinning of skin and stretch marks&lt;br /&gt;
|-&lt;br /&gt;
!Ophthalmic side effects&lt;br /&gt;
| Glaucoma, partial loss of vision due to opacity in the lens of the eye (cataracts)&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
Fludrocortisone is readily absorbed from the gastrointestinal tract. The plasma half-life is about 3.5 hours, but fludrocortisone has a more prolonged biological half-life of 18 to 36 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Management ==&lt;br /&gt;
===Monitoring=== &lt;br /&gt;
*Elderly (close supervision required particularly on long-term treatment)&lt;br /&gt;
*Frequent monitoring required if history of tuberculosis (or X-ray changes)&lt;br /&gt;
*Blood sugar level, blood pressure, mood change&lt;br /&gt;
*Monitoring of the fluid intake and output, and daily weight records may give early warning of fluid retention&lt;br /&gt;
*Sodium intake may need to be reduced and calcium and potassium supplements may be necessary&lt;br /&gt;
*Back pain may signify osteoporosis&lt;br /&gt;
*Plasma renin, sodium, and potassium is checked through blood tests to verify that the correct dosage is reached&lt;br /&gt;
&lt;br /&gt;
=== Drug interaction ===&lt;br /&gt;
Interactions do not generally apply to steroid used for topical action including inhalation, unless specified. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Drugs given with steroid &lt;br /&gt;
!Potential adverse drug interactions&lt;br /&gt;
|-&lt;br /&gt;
| NSAIDs&lt;br /&gt;
| Increased risk of gastro-intestinal bleeding&lt;br /&gt;
|-&lt;br /&gt;
| Rifampicin&lt;br /&gt;
| Accelerate metabolism of fludrocortisone so reduce its effects &lt;br /&gt;
|-&lt;br /&gt;
| Antidiabetics&lt;br /&gt;
| Antagonize hypoglycemic effect, so may need to increase antidiabetic dosage &lt;br /&gt;
|-&lt;br /&gt;
| Antiepileptics such as carbamazepine, phenobarbitone, phenytoin&lt;br /&gt;
| Accelerate metabolism of fludrocortisone so reduce its effects &lt;br /&gt;
|-&lt;br /&gt;
| Antifungal e.g. amphotericin&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Antiviral e.g ritonavir&lt;br /&gt;
| Increase plasma concentration of steroid – increased risk of adrenal suppression&lt;br /&gt;
|-&lt;br /&gt;
| Digoxin&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Diuretics e.g. frusemide, hydrochlorothiazide&lt;br /&gt;
| Antagonize diuretic effect; increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Oral contraceptive (oestrogens)&lt;br /&gt;
| Increase plasma concentration of steroid&lt;br /&gt;
|-&lt;br /&gt;
| Theophylline&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
=== Caution ===&lt;br /&gt;
*Osteoporosis (post-menopausal women at special risk)&lt;br /&gt;
*Recent myocardial infarction, congestive heart failure&lt;br /&gt;
*Glaucoma (including family history)&lt;br /&gt;
*Ocular herpes simplex – risk of corneal perforation&lt;br /&gt;
*Psychiatric disorders (particularly if history of steroid-induced psychosis)&lt;br /&gt;
*Epilepsy&lt;br /&gt;
*Peptic ulcer&lt;br /&gt;
*Hypothyroidism&lt;br /&gt;
*Ulcerative colitis&lt;br /&gt;
*Diverticulitis&lt;br /&gt;
*Thromboembolic disorders&lt;br /&gt;
&lt;br /&gt;
=== Contraindication ===&lt;br /&gt;
*acute infections&lt;br /&gt;
*patients with active or doubtfully quiescent tuberculosis&lt;br /&gt;
*concurrent treatment live virus vaccines for at least 3 months afterwards&lt;br /&gt;
=== Hepatic impairment ===&lt;br /&gt;
When steroids are administered orally or parenterally, the plasma-drug concentration may be increased in patients with hepatic impairment. The patient should be monitored closely.&lt;br /&gt;
=== Renal impairment ===&lt;br /&gt;
Should be used with caution in patients with renal impairment. &lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
It is not yet clear if use of fludrocortisone during pregnancy is safe for the fetus.&lt;br /&gt;
&lt;br /&gt;
=== Note ===&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Prolonged use of steroid&lt;br /&gt;
! advice to patient&lt;br /&gt;
|-&lt;br /&gt;
| Increase susceptibility to infection&lt;br /&gt;
| Avoid contact with people who have chickenpox, shingles, or measles.&lt;br /&gt;
|-&lt;br /&gt;
| Suppresses the endogenous secretion of corticotrophin by the anterior pituitary, resulting the adrenal cortex becomes atrophied. &lt;br /&gt;
If given for more than 3 weeks, treatment MUST be stopped gradually. &lt;br /&gt;
| Patient must mention the course of steroid when receiving treatment for intercurrent illnesses or going through trauma such as surgery.&lt;br /&gt;
|}&lt;br /&gt;
== FAQ ==&lt;br /&gt;
=== How should I take the tablet? ===&lt;br /&gt;
The tablet MUST be taken with or after food to help reduce GI side-effects.&lt;br /&gt;
=== What should I avoid while taking? ===&lt;br /&gt;
Avoid abruptly discontinue the medication. &lt;br /&gt;
Should not be taken with NSAIDs. &lt;br /&gt;
=== What happen if I overdose? ===&lt;br /&gt;
Contact your primary care doctor.&lt;br /&gt;
If emergency situation, call 999&lt;br /&gt;
=== What happen if I miss a dose? ===&lt;br /&gt;
Take it as soon as you &lt;br /&gt;
remember. If it is near the time &lt;br /&gt;
of the next dose, skip the missed &lt;br /&gt;
dose. Take your next dose at the &lt;br /&gt;
regular time. Do not double the &lt;br /&gt;
dose to catch up.&lt;br /&gt;
IV, IM and IA: administered by professionals&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=421</id>
		<title>Fludrocortisone</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=421"/>
		<updated>2020-09-05T12:12:11Z</updated>

		<summary type="html">&lt;p&gt;Annayung: /* Drug interaction */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
== Introduction ==&lt;br /&gt;
&lt;br /&gt;
Fludrocortisone is a steroid with potent mineralocorticoid activity. &lt;br /&gt;
It is used to treat:&lt;br /&gt;
*adrenocortical insufficiency&lt;br /&gt;
*postural hypotension&lt;br /&gt;
*adrenogenital syndrome&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Generic Name&lt;br /&gt;
!HA Code&lt;br /&gt;
!Legal Classification&lt;br /&gt;
|-&lt;br /&gt;
|Fludrocortisone Acetate Tablet 100mcg&lt;br /&gt;
|FLUD01&lt;br /&gt;
|P1S1S3&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Brand Name&lt;br /&gt;
!HK Reg Number&lt;br /&gt;
!Active Ingredients&lt;br /&gt;
|-&lt;br /&gt;
|FLORINEF TABLET 0.1mg&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|HK-00036&lt;br /&gt;
|fludrocortisone acetate&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Fludrocortisone is a corticosteroid with glucocorticoid and highly potent mineralocorticoid activity.&lt;br /&gt;
&lt;br /&gt;
== Dosage ==&lt;br /&gt;
Fludrocortisone is used, usually with hydrocortisone, for replacement therapy in adrenocortical insufficiency. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Replacement therapy in adrenal insufficiency&lt;br /&gt;
| Oral: 50-300 micrograms daily &lt;br /&gt;
|-&lt;br /&gt;
! severe orthostatic hypotension&lt;br /&gt;
| Oral: 50-300 micrograms daily&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
It is also used ear drops in concentration of 0.1%.&lt;br /&gt;
== Side Effects ==&lt;br /&gt;
Fludrocortisone acetate has glucocorticoid actions about 10 times as potent as hydrocortisone and mineralocorticoid effects more than 100 times as potent. &lt;br /&gt;
Adverse effects are mainly those due to mineralocorticoid activity:&lt;br /&gt;
*sodium and water retention&lt;br /&gt;
*swelling due to fluid retention (oedema)&lt;br /&gt;
*hypertension&lt;br /&gt;
*increased excretion of potassium leading to hypokalaemia&lt;br /&gt;
*heart failure may be induced in susceptible patients&lt;br /&gt;
Other side-effects include:&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!steroid-induced diabetes&lt;br /&gt;
| Raised blood sugar level&lt;br /&gt;
|-&lt;br /&gt;
!Osteoporosis, muscle wasting and weakenss&lt;br /&gt;
| Is a danger, particularly in the elderly, as it can result in osteoporotic fractures for example of the hip or vertebrae&lt;br /&gt;
|-&lt;br /&gt;
! Susceptibility to infection&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
! Disturbances of the gut&lt;br /&gt;
| Indigestion, peptic ulcer, distension of the abdomen&lt;br /&gt;
|-&lt;br /&gt;
!Suppression of growth in children&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
!Endocrine side effects&lt;br /&gt;
|Menstrual irregularities , hirsutism (increased hair growth), weight gain&lt;br /&gt;
|-&lt;br /&gt;
!Neuropsychiatric side effects&lt;br /&gt;
| Aggravation of schizophrenia, aggravation of epilepsy, insomnia, irritability, depression&lt;br /&gt;
|-&lt;br /&gt;
!Dermatological side effects&lt;br /&gt;
| Easy bruising, impaired wound healing, thinning of skin and stretch marks&lt;br /&gt;
|-&lt;br /&gt;
!Ophthalmic side effects&lt;br /&gt;
| Glaucoma, partial loss of vision due to opacity in the lens of the eye (cataracts)&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
Fludrocortisone is readily absorbed from the gastrointestinal tract. The plasma half-life is about 3.5 hours, but fludrocortisone has a more prolonged biological half-life of 18 to 36 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Management ==&lt;br /&gt;
===Monitoring=== &lt;br /&gt;
*Elderly (close supervision required particularly on long-term treatment)&lt;br /&gt;
*Frequent monitoring required if history of tuberculosis (or X-ray changes)&lt;br /&gt;
*Blood sugar level, blood pressure, mood change&lt;br /&gt;
*Monitoring of the fluid intake and output, and daily weight records may give early warning of fluid retention&lt;br /&gt;
*Sodium intake may need to be reduced and calcium and potassium supplements may be necessary&lt;br /&gt;
*Back pain may signify osteoporosis&lt;br /&gt;
*Plasma renin, sodium, and potassium is checked through blood tests to verify that the correct dosage is reached&lt;br /&gt;
&lt;br /&gt;
=== Drug interaction ===&lt;br /&gt;
Interactions do not generally apply to steroid used for topical action including inhalation, unless specified. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Drugs given with steroid &lt;br /&gt;
!Potential adverse drug interactions&lt;br /&gt;
|-&lt;br /&gt;
| NSAIDs&lt;br /&gt;
| Increased risk of gastro-intestinal bleeding&lt;br /&gt;
|-&lt;br /&gt;
| Rifampicin&lt;br /&gt;
| Accelerate metabolism of fludrocortisone so reduce its effects &lt;br /&gt;
|-&lt;br /&gt;
| Antidiabetics&lt;br /&gt;
| Antagonize hypoglycemic effect, so may need to increase antidiabetic dosage &lt;br /&gt;
|-&lt;br /&gt;
| Antiepileptics such as carbamazepine, phenobarbitone, phenytoin&lt;br /&gt;
| Accelerate metabolism of fludrocortisone so reduce its effects &lt;br /&gt;
|-&lt;br /&gt;
| Antifungal e.g. amphotericin&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Antiviral e.g ritonavir&lt;br /&gt;
| Increase plasma concentration of steroid – increased risk of adrenal suppression&lt;br /&gt;
|-&lt;br /&gt;
| Digoxin&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Diuretics e.g. frusemide, hydrochlorothiazide&lt;br /&gt;
| Antagonize diuretic effect; increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Oral contraceptive (oestrogens)&lt;br /&gt;
| Increase plasma concentration of steroid&lt;br /&gt;
|-&lt;br /&gt;
| Theophylline&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
=== Caution ===&lt;br /&gt;
*Osteoporosis (post-menopausal women at special risk)&lt;br /&gt;
*Recent myocardial infarction, congestive heart failure&lt;br /&gt;
*Glaucoma (including family history)&lt;br /&gt;
*Ocular herpes simplex – risk of corneal perforation&lt;br /&gt;
*Psychiatric disorders (particularly if history of steroid-induced psychosis)&lt;br /&gt;
*Epilepsy&lt;br /&gt;
*Peptic ulcer&lt;br /&gt;
*Hypothyroidism&lt;br /&gt;
*Ulcerative colitis&lt;br /&gt;
*Diverticulitis&lt;br /&gt;
*Thromboembolic disorders&lt;br /&gt;
&lt;br /&gt;
=== Contraindication ===&lt;br /&gt;
*acute infections&lt;br /&gt;
*patients with active or doubtfully quiescent tuberculosis&lt;br /&gt;
*concurrent treatment live virus vaccines for at least 3 months afterwards&lt;br /&gt;
=== Hepatic impairment ===&lt;br /&gt;
When steroids are administered orally or parenterally, the plasma-drug concentration may be increased in patients with hepatic impairment. The patient should be monitored closely.&lt;br /&gt;
=== Renal impairment ===&lt;br /&gt;
Should be used with caution in patients with renal impairment. &lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
It is not yet clear if use of fludrocortisone during pregnancy is safe for the fetus.&lt;br /&gt;
&lt;br /&gt;
=== Note ===&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Prolonged use of steroid&lt;br /&gt;
! advice to patient&lt;br /&gt;
|-&lt;br /&gt;
| Increase susceptibility to infection&lt;br /&gt;
| Avoid contact with people who have chickenpox, shingles, or measles.&lt;br /&gt;
|-&lt;br /&gt;
| Suppresses the endogenous secretion of corticotrophin by the anterior pituitary, resulting the adrenal cortex becomes atrophied. &lt;br /&gt;
If given for more than 3 weeks, treatment MUST be stopped gradually. &lt;br /&gt;
| Patient must mention the course of steroid when receiving treatment for intercurrent illnesses or going through trauma such as surgery.&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=420</id>
		<title>Fludrocortisone</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=420"/>
		<updated>2020-09-05T12:09:24Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
== Introduction ==&lt;br /&gt;
&lt;br /&gt;
Fludrocortisone is a steroid with potent mineralocorticoid activity. &lt;br /&gt;
It is used to treat:&lt;br /&gt;
*adrenocortical insufficiency&lt;br /&gt;
*postural hypotension&lt;br /&gt;
*adrenogenital syndrome&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Generic Name&lt;br /&gt;
!HA Code&lt;br /&gt;
!Legal Classification&lt;br /&gt;
|-&lt;br /&gt;
|Fludrocortisone Acetate Tablet 100mcg&lt;br /&gt;
|FLUD01&lt;br /&gt;
|P1S1S3&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Brand Name&lt;br /&gt;
!HK Reg Number&lt;br /&gt;
!Active Ingredients&lt;br /&gt;
|-&lt;br /&gt;
|FLORINEF TABLET 0.1mg&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|HK-00036&lt;br /&gt;
|fludrocortisone acetate&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Fludrocortisone is a corticosteroid with glucocorticoid and highly potent mineralocorticoid activity.&lt;br /&gt;
&lt;br /&gt;
== Dosage ==&lt;br /&gt;
Fludrocortisone is used, usually with hydrocortisone, for replacement therapy in adrenocortical insufficiency. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Replacement therapy in adrenal insufficiency&lt;br /&gt;
| Oral: 50-300 micrograms daily &lt;br /&gt;
|-&lt;br /&gt;
! severe orthostatic hypotension&lt;br /&gt;
| Oral: 50-300 micrograms daily&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
It is also used ear drops in concentration of 0.1%.&lt;br /&gt;
== Side Effects ==&lt;br /&gt;
Fludrocortisone acetate has glucocorticoid actions about 10 times as potent as hydrocortisone and mineralocorticoid effects more than 100 times as potent. &lt;br /&gt;
Adverse effects are mainly those due to mineralocorticoid activity:&lt;br /&gt;
*sodium and water retention&lt;br /&gt;
*swelling due to fluid retention (oedema)&lt;br /&gt;
*hypertension&lt;br /&gt;
*increased excretion of potassium leading to hypokalaemia&lt;br /&gt;
*heart failure may be induced in susceptible patients&lt;br /&gt;
Other side-effects include:&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!steroid-induced diabetes&lt;br /&gt;
| Raised blood sugar level&lt;br /&gt;
|-&lt;br /&gt;
!Osteoporosis, muscle wasting and weakenss&lt;br /&gt;
| Is a danger, particularly in the elderly, as it can result in osteoporotic fractures for example of the hip or vertebrae&lt;br /&gt;
|-&lt;br /&gt;
! Susceptibility to infection&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
! Disturbances of the gut&lt;br /&gt;
| Indigestion, peptic ulcer, distension of the abdomen&lt;br /&gt;
|-&lt;br /&gt;
!Suppression of growth in children&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
!Endocrine side effects&lt;br /&gt;
|Menstrual irregularities , hirsutism (increased hair growth), weight gain&lt;br /&gt;
|-&lt;br /&gt;
!Neuropsychiatric side effects&lt;br /&gt;
| Aggravation of schizophrenia, aggravation of epilepsy, insomnia, irritability, depression&lt;br /&gt;
|-&lt;br /&gt;
!Dermatological side effects&lt;br /&gt;
| Easy bruising, impaired wound healing, thinning of skin and stretch marks&lt;br /&gt;
|-&lt;br /&gt;
!Ophthalmic side effects&lt;br /&gt;
| Glaucoma, partial loss of vision due to opacity in the lens of the eye (cataracts)&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
Fludrocortisone is readily absorbed from the gastrointestinal tract. The plasma half-life is about 3.5 hours, but fludrocortisone has a more prolonged biological half-life of 18 to 36 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Management ==&lt;br /&gt;
===Monitoring=== &lt;br /&gt;
*Elderly (close supervision required particularly on long-term treatment)&lt;br /&gt;
*Frequent monitoring required if history of tuberculosis (or X-ray changes)&lt;br /&gt;
*Blood sugar level, blood pressure, mood change&lt;br /&gt;
*Monitoring of the fluid intake and output, and daily weight records may give early warning of fluid retention&lt;br /&gt;
*Sodium intake may need to be reduced and calcium and potassium supplements may be necessary&lt;br /&gt;
*Back pain may signify osteoporosis&lt;br /&gt;
*Plasma renin, sodium, and potassium is checked through blood tests to verify that the correct dosage is reached&lt;br /&gt;
&lt;br /&gt;
=== Drug interaction ===&lt;br /&gt;
Interactions do not generally apply to steroid used for topical action including inhalation, unless specified. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Drugs given with steroid &lt;br /&gt;
!Potential adverse drug interactions&lt;br /&gt;
| NSAIDs&lt;br /&gt;
| Increased risk of gastro-intestinal bleeding&lt;br /&gt;
|-&lt;br /&gt;
| Rifampicin&lt;br /&gt;
| Accelerate metabolism of fludrocortisone so reduce its effects &lt;br /&gt;
|-&lt;br /&gt;
| Antidiabetics&lt;br /&gt;
| Antagonize hypoglycemic effect, so may need to increase antidiabetic dosage &lt;br /&gt;
|-&lt;br /&gt;
| Antiepileptics such as carbamazepine, phenobarbitone, phenytoin&lt;br /&gt;
| Accelerate metabolism of fludrocortisone so reduce its effects &lt;br /&gt;
|-&lt;br /&gt;
| Antifungal e.g. amphotericin&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Antiviral e.g ritonavir&lt;br /&gt;
| Increase plasma concentration of steroid – increased risk of adrenal suppression&lt;br /&gt;
|-&lt;br /&gt;
| Digoxin&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Diuretics e.g. frusemide, hydrochlorothiazide&lt;br /&gt;
| Antagonize diuretic effect; increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Oral contraceptive (oestrogens)&lt;br /&gt;
| Increase plasma concentration of steroid&lt;br /&gt;
|-&lt;br /&gt;
| Theophylline&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
=== Caution ===&lt;br /&gt;
*Osteoporosis (post-menopausal women at special risk)&lt;br /&gt;
*Recent myocardial infarction, congestive heart failure&lt;br /&gt;
*Glaucoma (including family history)&lt;br /&gt;
*Ocular herpes simplex – risk of corneal perforation&lt;br /&gt;
*Psychiatric disorders (particularly if history of steroid-induced psychosis)&lt;br /&gt;
*Epilepsy&lt;br /&gt;
*Peptic ulcer&lt;br /&gt;
*Hypothyroidism&lt;br /&gt;
*Ulcerative colitis&lt;br /&gt;
*Diverticulitis&lt;br /&gt;
*Thromboembolic disorders&lt;br /&gt;
&lt;br /&gt;
=== Contraindication ===&lt;br /&gt;
*acute infections&lt;br /&gt;
*patients with active or doubtfully quiescent tuberculosis&lt;br /&gt;
*concurrent treatment live virus vaccines for at least 3 months afterwards&lt;br /&gt;
=== Hepatic impairment ===&lt;br /&gt;
When steroids are administered orally or parenterally, the plasma-drug concentration may be increased in patients with hepatic impairment. The patient should be monitored closely.&lt;br /&gt;
=== Renal impairment ===&lt;br /&gt;
Should be used with caution in patients with renal impairment. &lt;br /&gt;
&lt;br /&gt;
=== Pregnancy ===&lt;br /&gt;
It is not yet clear if use of fludrocortisone during pregnancy is safe for the fetus.&lt;br /&gt;
&lt;br /&gt;
=== Note ===&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Prolonged use of steroid&lt;br /&gt;
! advice to patient&lt;br /&gt;
|-&lt;br /&gt;
| Increase susceptibility to infection&lt;br /&gt;
| Avoid contact with people who have chickenpox, shingles, or measles.&lt;br /&gt;
|-&lt;br /&gt;
| Suppresses the endogenous secretion of corticotrophin by the anterior pituitary, resulting the adrenal cortex becomes atrophied. &lt;br /&gt;
If given for more than 3 weeks, treatment MUST be stopped gradually. &lt;br /&gt;
| Patient must mention the course of steroid when receiving treatment for intercurrent illnesses or going through trauma such as surgery.&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=419</id>
		<title>Fludrocortisone</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=419"/>
		<updated>2020-09-05T11:53:03Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
== Introduction ==&lt;br /&gt;
&lt;br /&gt;
Fludrocortisone is a steroid with potent mineralocorticoid activity. &lt;br /&gt;
It is used to treat:&lt;br /&gt;
*adrenocortical insufficiency&lt;br /&gt;
*postural hypotension&lt;br /&gt;
*adrenogenital syndrome&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Generic Name&lt;br /&gt;
!HA Code&lt;br /&gt;
!Legal Classification&lt;br /&gt;
|-&lt;br /&gt;
|Fludrocortisone Acetate Tablet 100mcg&lt;br /&gt;
|FLUD01&lt;br /&gt;
|P1S1S3&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Brand Name&lt;br /&gt;
!HK Reg Number&lt;br /&gt;
!Active Ingredients&lt;br /&gt;
|-&lt;br /&gt;
|FLORINEF TABLET 0.1mg&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|HK-00036&lt;br /&gt;
|fludrocortisone acetate&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Fludrocortisone is a corticosteroid with glucocorticoid and highly potent mineralocorticoid activity.&lt;br /&gt;
&lt;br /&gt;
== Dosage ==&lt;br /&gt;
Fludrocortisone is used, usually with hydrocortisone, for replacement therapy in adrenocortical insufficiency. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Replacement therapy in adrenal insufficiency&lt;br /&gt;
| Oral: 50-300 micrograms daily &lt;br /&gt;
|-&lt;br /&gt;
! severe orthostatic hypotension&lt;br /&gt;
| Oral: 50-300 micrograms daily&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
It is also used ear drops in concentration of 0.1%.&lt;br /&gt;
== Side Effects ==&lt;br /&gt;
Fludrocortisone acetate has glucocorticoid actions about 10 times as potent as hydrocortisone and mineralocorticoid effects more than 100 times as potent. &lt;br /&gt;
Adverse effects are mainly those due to mineralocorticoid activity:&lt;br /&gt;
*sodium and water retention&lt;br /&gt;
*swelling due to fluid retention (oedema)&lt;br /&gt;
*hypertension&lt;br /&gt;
*increased excretion of potassium leading to hypokalaemia&lt;br /&gt;
*heart failure may be induced in susceptible patients&lt;br /&gt;
Other side-effects include:&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!steroid-induced diabetes&lt;br /&gt;
| Raised blood sugar level&lt;br /&gt;
|-&lt;br /&gt;
!Osteoporosis, muscle wasting and weakenss&lt;br /&gt;
| which is a danger, particularly in the elderly, as it can result in osteoporotic fractures for example of the hip or vertebrae&lt;br /&gt;
|-&lt;br /&gt;
! Susceptibility to infection&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
! Disturbances of the gut&lt;br /&gt;
| Indigestion, peptic ulcer, distension of the abdomen&lt;br /&gt;
|-&lt;br /&gt;
!Suppression of growth in children&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
!Endocrine side effects&lt;br /&gt;
|menstrual irregularities , hirsutism (increased hair growth), weight gain&lt;br /&gt;
|-&lt;br /&gt;
!Neuropsychiatric side effects&lt;br /&gt;
| aggravation of schizophrenia, aggravation of epilepsy, insomnia, irritability, depression&lt;br /&gt;
|-&lt;br /&gt;
!Dermatological side effects&lt;br /&gt;
| easy bruising, impaired wound healing, thinning of skin and stretch marks&lt;br /&gt;
|-&lt;br /&gt;
!Ophthalmic side effects&lt;br /&gt;
| glaucoma, partial loss of vision due to opacity in the lens of the eye (cataracts)&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
Fludrocortisone is readily absorbed from the gastrointestinal tract. The plasma half-life is about 3.5 hours, but fludrocortisone has a more prolonged biological half-life of 18 to 36 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Management ==&lt;br /&gt;
===Monitoring=== &lt;br /&gt;
*Elderly (close supervision required particularly on long-term treatment)&lt;br /&gt;
*Frequent monitoring required if history of tuberculosis (or X-ray changes)&lt;br /&gt;
*blood sugar level, blood pressure, mood change&lt;br /&gt;
*monitoring of the fluid intake and output, and daily weight records may give early warning of fluid retention&lt;br /&gt;
*Sodium intake may need to be reduced and calcium and potassium supplements may be necessary&lt;br /&gt;
*Back pain may signify osteoporosis&lt;br /&gt;
*Plasma renin, sodium, and potassium is checked through blood tests to verify that the correct dosage is reached&lt;br /&gt;
&lt;br /&gt;
=== Drug interaction ===&lt;br /&gt;
Interactions do not generally apply to steroid used for topical action including inhalation, unless specified. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Drugs given with steroid &lt;br /&gt;
!Potential adverse drug interactions&lt;br /&gt;
| NSAIDs&lt;br /&gt;
| Increased risk of gastro-intestinal bleeding&lt;br /&gt;
|-&lt;br /&gt;
| Rifampicin&lt;br /&gt;
| Accelerate metabolism of fludrocortisone so reduce its effects &lt;br /&gt;
|-&lt;br /&gt;
| Antidiabetics&lt;br /&gt;
| Antagonize hypoglycemic effect, so may need to increase antidiabetic dosage &lt;br /&gt;
|-&lt;br /&gt;
| Antiepileptics such as carbamazepine, phenobarbitone, phenytoin&lt;br /&gt;
| Accelerate metabolism of fludrocortisone so reduce its effects &lt;br /&gt;
|-&lt;br /&gt;
| Antifungal e.g. amphotericin&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Antiviral e.g ritonavir&lt;br /&gt;
| Increase plasma concentration of steroid – increased risk of adrenal suppression&lt;br /&gt;
|-&lt;br /&gt;
| Digoxin&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Diuretics e.g. frusemide, hydrochlorothiazide&lt;br /&gt;
| antagonize diuretic effect; -	increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Oral contraceptive (oestrogens)&lt;br /&gt;
| Increase plasma concentration of steroid&lt;br /&gt;
|-&lt;br /&gt;
| Theophylline&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=418</id>
		<title>Fludrocortisone</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=418"/>
		<updated>2020-09-05T11:48:35Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
== Introduction ==&lt;br /&gt;
&lt;br /&gt;
Fludrocortisone is a steroid with potent mineralocorticoid activity. &lt;br /&gt;
It is used to treat:&lt;br /&gt;
*adrenocortical insufficiency&lt;br /&gt;
*postural hypotension&lt;br /&gt;
*adrenogenital syndrome&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Generic Name&lt;br /&gt;
!HA Code&lt;br /&gt;
!Legal Classification&lt;br /&gt;
|-&lt;br /&gt;
|Fludrocortisone Acetate Tablet 100mcg&lt;br /&gt;
|FLUD01&lt;br /&gt;
|P1S1S3&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Brand Name&lt;br /&gt;
!HK Reg Number&lt;br /&gt;
!Active Ingredients&lt;br /&gt;
|-&lt;br /&gt;
|FLORINEF TABLET 0.1mg&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|HK-00036&lt;br /&gt;
|fludrocortisone acetate&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Fludrocortisone is a corticosteroid with glucocorticoid and highly potent mineralocorticoid activity.&lt;br /&gt;
&lt;br /&gt;
== Dosage ==&lt;br /&gt;
Fludrocortisone is used, usually with hydrocortisone, for replacement therapy in adrenocortical insufficiency. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Replacement therapy in adrenal insufficiency&lt;br /&gt;
| Oral: 50-300 micrograms daily &lt;br /&gt;
|-&lt;br /&gt;
! severe orthostatic hypotension&lt;br /&gt;
| Oral: 50-300 micrograms daily&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
It is also used ear drops in concentration of 0.1%.&lt;br /&gt;
== Side Effects ==&lt;br /&gt;
Fludrocortisone acetate has glucocorticoid actions about 10 times as potent as hydrocortisone and mineralocorticoid effects more than 100 times as potent. &lt;br /&gt;
Adverse effects are mainly those due to mineralocorticoid activity:&lt;br /&gt;
*sodium and water retention&lt;br /&gt;
*swelling due to fluid retention (oedema)&lt;br /&gt;
*hypertension&lt;br /&gt;
*increased excretion of potassium leading to hypokalaemia&lt;br /&gt;
*heart failure may be induced in susceptible patients&lt;br /&gt;
Other side-effects include:&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!steroid-induced diabetes&lt;br /&gt;
| Raised blood sugar level&lt;br /&gt;
|-&lt;br /&gt;
!Osteoporosis, muscle wasting and weakenss&lt;br /&gt;
| which is a danger, particularly in the elderly, as it can result in osteoporotic fractures for example of the hip or vertebrae&lt;br /&gt;
|-&lt;br /&gt;
! Susceptibility to infection&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
! Disturbances of the gut&lt;br /&gt;
| Indigestion, peptic ulcer, distension of the abdomen&lt;br /&gt;
|-&lt;br /&gt;
!Suppression of growth in children&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
!Endocrine side effects&lt;br /&gt;
|menstrual irregularities , hirsutism (increased hair growth), weight gain&lt;br /&gt;
|-&lt;br /&gt;
!Neuropsychiatric side effects&lt;br /&gt;
| aggravation of schizophrenia, aggravation of epilepsy, insomnia, irritability, depression&lt;br /&gt;
|-&lt;br /&gt;
!Dermatological side effects&lt;br /&gt;
| easy bruising, impaired wound healing, thinning of skin and stretch marks&lt;br /&gt;
|-&lt;br /&gt;
!Ophthalmic side effects&lt;br /&gt;
| glaucoma, partial loss of vision due to opacity in the lens of the eye (cataracts)&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
Fludrocortisone is readily absorbed from the gastrointestinal tract. The plasma half-life is about 3.5 hours, but fludrocortisone has a more prolonged biological half-life of 18 to 36 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Management ==&lt;br /&gt;
===Monitoring=== &lt;br /&gt;
*Elderly (close supervision required particularly on long-term treatment)&lt;br /&gt;
*Frequent monitoring required if history of tuberculosis (or X-ray changes)&lt;br /&gt;
*blood sugar level, blood pressure, mood change&lt;br /&gt;
*monitoring of the fluid intake and output, and daily weight records may give early warning of fluid retention&lt;br /&gt;
*Sodium intake may need to be reduced and calcium and potassium supplements may be necessary&lt;br /&gt;
*Back pain may signify osteoporosis&lt;br /&gt;
*Plasma renin, sodium, and potassium is checked through blood tests to verify that the correct dosage is reached&lt;br /&gt;
&lt;br /&gt;
=== Drug interaction ===&lt;br /&gt;
Interactions do not generally apply to steroid used for topical action including inhalation, unless specified. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Drugs given with steroid &lt;br /&gt;
!Potential adverse drug interactions&lt;br /&gt;
| NSAIDs&lt;br /&gt;
| Increased risk of gastro-intestinal bleeding&lt;br /&gt;
|-&lt;br /&gt;
| Rifampicin&lt;br /&gt;
| Accelerate metabolism of fludrocortisone so reduce its effects &lt;br /&gt;
|-&lt;br /&gt;
| Antidiabetics&lt;br /&gt;
| Antagonize hypoglycemic effect, so may need to increase antidiabetic dosage &lt;br /&gt;
|-&lt;br /&gt;
| Antiepileptics such as carbamazepine, phenobarbitone, phenytoin&lt;br /&gt;
| Accelerate metabolism of fludrocortisone so reduce its effects &lt;br /&gt;
|-&lt;br /&gt;
| Antifungal e.g. amphotericin&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Antiviral e.g ritonavir&lt;br /&gt;
| Increase plasma concentration of steroid – increased risk of adrenal suppression&lt;br /&gt;
|-&lt;br /&gt;
| Digoxin&lt;br /&gt;
| Increased risk of hypokalaemia&lt;br /&gt;
|-&lt;br /&gt;
| Diuretics&lt;br /&gt;
&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=417</id>
		<title>Fludrocortisone</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=417"/>
		<updated>2020-09-05T11:39:42Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
== Introduction ==&lt;br /&gt;
&lt;br /&gt;
Fludrocortisone is a steroid with potent mineralocorticoid activity. &lt;br /&gt;
It is used to treat:&lt;br /&gt;
*adrenocortical insufficiency&lt;br /&gt;
*postural hypotension&lt;br /&gt;
*adrenogenital syndrome&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Generic Name&lt;br /&gt;
!HA Code&lt;br /&gt;
!Legal Classification&lt;br /&gt;
|-&lt;br /&gt;
|Fludrocortisone Acetate Tablet 100mcg&lt;br /&gt;
|FLUD01&lt;br /&gt;
|P1S1S3&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Brand Name&lt;br /&gt;
!HK Reg Number&lt;br /&gt;
!Active Ingredients&lt;br /&gt;
|-&lt;br /&gt;
|FLORINEF TABLET 0.1mg&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|HK-00036&lt;br /&gt;
|fludrocortisone acetate&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Fludrocortisone is a corticosteroid with glucocorticoid and highly potent mineralocorticoid activity.&lt;br /&gt;
&lt;br /&gt;
== Dosage ==&lt;br /&gt;
Fludrocortisone is used, usually with hydrocortisone, for replacement therapy in adrenocortical insufficiency. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Replacement therapy in adrenal insufficiency&lt;br /&gt;
| Oral: 50-300 micrograms daily &lt;br /&gt;
|-&lt;br /&gt;
! severe orthostatic hypotension&lt;br /&gt;
| Oral: 50-300 micrograms daily&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
It is also used ear drops in concentration of 0.1%.&lt;br /&gt;
== Side Effects ==&lt;br /&gt;
Fludrocortisone acetate has glucocorticoid actions about 10 times as potent as hydrocortisone and mineralocorticoid effects more than 100 times as potent. &lt;br /&gt;
Adverse effects are mainly those due to mineralocorticoid activity:&lt;br /&gt;
*sodium and water retention&lt;br /&gt;
*swelling due to fluid retention (oedema)&lt;br /&gt;
*hypertension&lt;br /&gt;
*increased excretion of potassium leading to hypokalaemia&lt;br /&gt;
*heart failure may be induced in susceptible patients&lt;br /&gt;
Other side-effects include:&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!steroid-induced diabetes&lt;br /&gt;
| Raised blood sugar level&lt;br /&gt;
|-&lt;br /&gt;
!Osteoporosis, muscle wasting and weakenss&lt;br /&gt;
| which is a danger, particularly in the elderly, as it can result in osteoporotic fractures for example of the hip or vertebrae&lt;br /&gt;
|-&lt;br /&gt;
! Susceptibility to infection&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
! Disturbances of the gut&lt;br /&gt;
| Indigestion, peptic ulcer, distension of the abdomen&lt;br /&gt;
|-&lt;br /&gt;
!Suppression of growth in children&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
!Endocrine side effects&lt;br /&gt;
|menstrual irregularities , hirsutism (increased hair growth), weight gain&lt;br /&gt;
|-&lt;br /&gt;
!Neuropsychiatric side effects&lt;br /&gt;
| aggravation of schizophrenia, aggravation of epilepsy, insomnia, irritability, depression&lt;br /&gt;
|-&lt;br /&gt;
!Dermatological side effects&lt;br /&gt;
| easy bruising, impaired wound healing, thinning of skin and stretch marks&lt;br /&gt;
|-&lt;br /&gt;
!Ophthalmic side effects&lt;br /&gt;
| glaucoma, partial loss of vision due to opacity in the lens of the eye (cataracts)&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
Fludrocortisone is readily absorbed from the gastrointestinal tract. The plasma half-life is about 3.5 hours, but fludrocortisone has a more prolonged biological half-life of 18 to 36 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Management ==&lt;br /&gt;
===Monitoring=== &lt;br /&gt;
*Elderly (close supervision required particularly on long-term treatment)&lt;br /&gt;
*Frequent monitoring required if history of tuberculosis (or X-ray changes)&lt;br /&gt;
*blood sugar level, blood pressure, mood change&lt;br /&gt;
*monitoring of the fluid intake and output, and daily weight records may give early warning of fluid retention&lt;br /&gt;
*Sodium intake may need to be reduced and calcium and potassium supplements may be necessary&lt;br /&gt;
*Back pain may signify osteoporosis&lt;br /&gt;
*Plasma renin, sodium, and potassium is checked through blood tests to verify that the correct dosage is reached&lt;br /&gt;
&lt;br /&gt;
=== Drug interaction ===&lt;br /&gt;
Interactions do not generally apply to steroid used for topical action including inhalation, unless specified. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Drugs given with steroid &lt;br /&gt;
!Potential adverse drug interactions&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=416</id>
		<title>Fludrocortisone</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=416"/>
		<updated>2020-09-05T11:36:40Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
== Introduction ==&lt;br /&gt;
&lt;br /&gt;
Fludrocortisone is a steroid with potent mineralocorticoid activity. &lt;br /&gt;
It is used to treat:&lt;br /&gt;
*adrenocortical insufficiency&lt;br /&gt;
*postural hypotension&lt;br /&gt;
*adrenogenital syndrome&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Generic Name&lt;br /&gt;
!HA Code&lt;br /&gt;
!Legal Classification&lt;br /&gt;
|-&lt;br /&gt;
|Fludrocortisone Acetate Tablet 100mcg&lt;br /&gt;
|FLUD01&lt;br /&gt;
|P1S1S3&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Brand Name&lt;br /&gt;
!HK Reg Number&lt;br /&gt;
!Active Ingredients&lt;br /&gt;
|-&lt;br /&gt;
|FLORINEF TABLET 0.1mg&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|HK-00036&lt;br /&gt;
|fludrocortisone acetate&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Fludrocortisone is a corticosteroid with glucocorticoid and highly potent mineralocorticoid activity.&lt;br /&gt;
&lt;br /&gt;
== Dosage ==&lt;br /&gt;
Fludrocortisone is used, usually with hydrocortisone, for replacement therapy in adrenocortical insufficiency. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Replacement therapy in adrenal insufficiency&lt;br /&gt;
| Oral: 50-300 micrograms daily &lt;br /&gt;
|-&lt;br /&gt;
! severe orthostatic hypotension&lt;br /&gt;
| Oral: 50-300 micrograms daily&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
It is also used ear drops in concentration of 0.1%.&lt;br /&gt;
== Side Effects ==&lt;br /&gt;
Fludrocortisone acetate has glucocorticoid actions about 10 times as potent as hydrocortisone and mineralocorticoid effects more than 100 times as potent. &lt;br /&gt;
Adverse effects are mainly those due to mineralocorticoid activity:&lt;br /&gt;
*sodium and water retention&lt;br /&gt;
*swelling due to fluid retention (oedema)&lt;br /&gt;
*hypertension&lt;br /&gt;
*increased excretion of potassium leading to hypokalaemia&lt;br /&gt;
*heart failure may be induced in susceptible patients&lt;br /&gt;
Other side-effects include:&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!steroid-induced diabetes&lt;br /&gt;
| Raised blood sugar level&lt;br /&gt;
|-&lt;br /&gt;
!Osteoporosis, muscle wasting and weakenss&lt;br /&gt;
| which is a danger, particularly in the elderly, as it can result in osteoporotic fractures for example of the hip or vertebrae&lt;br /&gt;
|-&lt;br /&gt;
! Susceptibility to infection&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
! Disturbances of the gut&lt;br /&gt;
| Indigestion, peptic ulcer, distension of the abdomen&lt;br /&gt;
|-&lt;br /&gt;
!Suppression of growth in children&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
!Endocrine side effects&lt;br /&gt;
|menstrual irregularities , hirsutism (increased hair growth), weight gain&lt;br /&gt;
|-&lt;br /&gt;
!Neuropsychiatric side effects&lt;br /&gt;
| aggravation of schizophrenia, aggravation of epilepsy, insomnia, irritability, depression&lt;br /&gt;
|-&lt;br /&gt;
!Dermatological side effects&lt;br /&gt;
| easy bruising, impaired wound healing, thinning of skin and stretch marks&lt;br /&gt;
|-&lt;br /&gt;
!Ophthalmic side effects&lt;br /&gt;
| glaucoma, partial loss of vision due to opacity in the lens of the eye (cataracts)&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
Fludrocortisone is readily absorbed from the gastrointestinal tract. The plasma half-life is about 3.5 hours, but fludrocortisone has a more prolonged biological half-life of 18 to 36 hours.&lt;br /&gt;
&lt;br /&gt;
== Drug Management ==&lt;br /&gt;
===Monitoring=== &lt;br /&gt;
*Elderly (close supervision required particularly on long-term treatment)&lt;br /&gt;
*Frequent monitoring required if history of tuberculosis (or X-ray changes)&lt;br /&gt;
*blood sugar level, blood pressure, mood change, &lt;br /&gt;
*monitoring of the fluid intake and output, and daily weight records may give early warning of fluid retention.&lt;br /&gt;
*Sodium intake may need to be reduced and calcium and potassium supplements may be necessary.&lt;br /&gt;
*Back pain may signify osteoporosis&lt;br /&gt;
*Plasma renin, sodium, and potassium is checked through blood tests to verify that the correct dosage is reached.&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=415</id>
		<title>Fludrocortisone</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=415"/>
		<updated>2020-09-05T11:33:58Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
== Introduction ==&lt;br /&gt;
&lt;br /&gt;
Fludrocortisone is a steroid with potent mineralocorticoid activity. &lt;br /&gt;
It is used to treat:&lt;br /&gt;
*adrenocortical insufficiency&lt;br /&gt;
*postural hypotension&lt;br /&gt;
*adrenogenital syndrome&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Generic Name&lt;br /&gt;
!HA Code&lt;br /&gt;
!Legal Classification&lt;br /&gt;
|-&lt;br /&gt;
|Fludrocortisone Acetate Tablet 100mcg&lt;br /&gt;
|FLUD01&lt;br /&gt;
|P1S1S3&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Brand Name&lt;br /&gt;
!HK Reg Number&lt;br /&gt;
!Active Ingredients&lt;br /&gt;
|-&lt;br /&gt;
|FLORINEF TABLET 0.1mg&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|HK-00036&lt;br /&gt;
|fludrocortisone acetate&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Fludrocortisone is a corticosteroid with glucocorticoid and highly potent mineralocorticoid activity.&lt;br /&gt;
&lt;br /&gt;
== Dosage ==&lt;br /&gt;
Fludrocortisone is used, usually with hydrocortisone, for replacement therapy in adrenocortical insufficiency. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Replacement therapy in adrenal insufficiency&lt;br /&gt;
| Oral: 50-300 micrograms daily &lt;br /&gt;
|-&lt;br /&gt;
! severe orthostatic hypotension&lt;br /&gt;
| Oral: 50-300 micrograms daily&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
It is also used ear drops in concentration of 0.1%.&lt;br /&gt;
== Side Effects ==&lt;br /&gt;
Fludrocortisone acetate has glucocorticoid actions about 10 times as potent as hydrocortisone and mineralocorticoid effects more than 100 times as potent. &lt;br /&gt;
Adverse effects are mainly those due to mineralocorticoid activity:&lt;br /&gt;
*sodium and water retention&lt;br /&gt;
*swelling due to fluid retention (oedema)&lt;br /&gt;
*hypertension&lt;br /&gt;
*increased excretion of potassium leading to hypokalaemia&lt;br /&gt;
*heart failure may be induced in susceptible patients&lt;br /&gt;
Other side-effects include:&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!steroid-induced diabetes&lt;br /&gt;
| Raised blood sugar level&lt;br /&gt;
|-&lt;br /&gt;
!Osteoporosis, muscle wasting and weakenss&lt;br /&gt;
| which is a danger, particularly in the elderly, as it can result in osteoporotic fractures for example of the hip or vertebrae&lt;br /&gt;
|-&lt;br /&gt;
! Susceptibility to infection&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
! Disturbances of the gut&lt;br /&gt;
| Indigestion, peptic ulcer, distension of the abdomen&lt;br /&gt;
|-&lt;br /&gt;
!Suppression of growth in children&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
!Endocrine side effects&lt;br /&gt;
|menstrual irregularities , hirsutism (increased hair growth), weight gain&lt;br /&gt;
|-&lt;br /&gt;
!Neuropsychiatric side effects&lt;br /&gt;
| aggravation of schizophrenia, aggravation of epilepsy, insomnia, irritability, depression&lt;br /&gt;
|-&lt;br /&gt;
!Dermatological side effects&lt;br /&gt;
| easy bruising, impaired wound healing, thinning of skin and stretch marks&lt;br /&gt;
|-&lt;br /&gt;
!Ophthalmic side effects&lt;br /&gt;
| glaucoma, partial loss of vision due to opacity in the lens of the eye (cataracts)&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=414</id>
		<title>Fludrocortisone</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=414"/>
		<updated>2020-09-05T11:28:01Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
== Introduction ==&lt;br /&gt;
&lt;br /&gt;
Fludrocortisone is a steroid with potent mineralocorticoid activity. &lt;br /&gt;
It is used to treat:&lt;br /&gt;
*adrenocortical insufficiency&lt;br /&gt;
*postural hypotension&lt;br /&gt;
*adrenogenital syndrome&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Generic Name&lt;br /&gt;
!HA Code&lt;br /&gt;
!Legal Classification&lt;br /&gt;
|-&lt;br /&gt;
|Fludrocortisone Acetate Tablet 100mcg&lt;br /&gt;
|FLUD01&lt;br /&gt;
|P1S1S3&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Brand Name&lt;br /&gt;
!HK Reg Number&lt;br /&gt;
!Active Ingredients&lt;br /&gt;
|-&lt;br /&gt;
|FLORINEF TABLET 0.1mg&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|HK-00036&lt;br /&gt;
|fludrocortisone acetate&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Fludrocortisone is a corticosteroid with glucocorticoid and highly potent mineralocorticoid activity.&lt;br /&gt;
&lt;br /&gt;
== Dosage ==&lt;br /&gt;
Fludrocortisone is used, usually with hydrocortisone, for replacement therapy in adrenocortical insufficiency. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Replacement therapy in adrenal insufficiency&lt;br /&gt;
| Oral: 50-300 micrograms daily &lt;br /&gt;
|-&lt;br /&gt;
! severe orthostatic hypotension&lt;br /&gt;
| Oral: 50-300 micrograms daily&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
It is also used ear drops in concentration of 0.1%.&lt;br /&gt;
== Side Effects ==&lt;br /&gt;
Fludrocortisone acetate has glucocorticoid actions about 10 times as potent as hydrocortisone and mineralocorticoid effects more than 100 times as potent. &lt;br /&gt;
Adverse effects are mainly those due to mineralocorticoid activity:&lt;br /&gt;
*sodium and water retention&lt;br /&gt;
*swelling due to fluid retention (oedema)&lt;br /&gt;
*hypertension&lt;br /&gt;
*increased excretion of potassium leading to hypokalaemia&lt;br /&gt;
*heart failure may be induced in susceptible patients&lt;br /&gt;
Other side-effects include:&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!steroid-induced diabetes&lt;br /&gt;
| Raised blood sugar level&lt;br /&gt;
|-&lt;br /&gt;
!Osteoporosis, muscle wasting and weakenss&lt;br /&gt;
| which is a danger, particularly in the elderly, as it can result in osteoporotic fractures for example of the hip or vertebrae&lt;br /&gt;
|-&lt;br /&gt;
! Susceptibility to infection&lt;br /&gt;
|&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=413</id>
		<title>Fludrocortisone</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=413"/>
		<updated>2020-09-05T11:26:32Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
== Introduction ==&lt;br /&gt;
&lt;br /&gt;
Fludrocortisone is a steroid with potent mineralocorticoid activity. &lt;br /&gt;
It is used to treat:&lt;br /&gt;
*adrenocortical insufficiency&lt;br /&gt;
*postural hypotension&lt;br /&gt;
*adrenogenital syndrome&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Generic Name&lt;br /&gt;
!HA Code&lt;br /&gt;
!Legal Classification&lt;br /&gt;
|-&lt;br /&gt;
|Fludrocortisone Acetate Tablet 100mcg&lt;br /&gt;
|FLUD01&lt;br /&gt;
|P1S1S3&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Brand Name&lt;br /&gt;
!HK Reg Number&lt;br /&gt;
!Active Ingredients&lt;br /&gt;
|-&lt;br /&gt;
|FLORINEF TABLET 0.1mg&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|HK-00036&lt;br /&gt;
|fludrocortisone acetate&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Fludrocortisone is a corticosteroid with glucocorticoid and highly potent mineralocorticoid activity.&lt;br /&gt;
&lt;br /&gt;
== Dosage ==&lt;br /&gt;
Fludrocortisone is used, usually with hydrocortisone, for replacement therapy in adrenocortical insufficiency. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Replacement therapy in adrenal insufficiency&lt;br /&gt;
| Oral: 50-300 micrograms daily &lt;br /&gt;
|-&lt;br /&gt;
! severe orthostatic hypotension&lt;br /&gt;
| Oral: 50-300 micrograms daily&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
It is also used ear drops in concentration of 0.1%.&lt;br /&gt;
== Side Effects ==&lt;br /&gt;
Fludrocortisone acetate has glucocorticoid actions about 10 times as potent as hydrocortisone and mineralocorticoid effects more than 100 times as potent. &lt;br /&gt;
Adverse effects are mainly those due to mineralocorticoid activity:&lt;br /&gt;
*sodium and water retention&lt;br /&gt;
*swelling due to fluid retention (oedema)&lt;br /&gt;
*hypertension&lt;br /&gt;
*increased excretion of potassium leading to hypokalaemia&lt;br /&gt;
*heart failure may be induced in susceptible patients&lt;br /&gt;
Other side-effects include:&lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
!steroid-induced diabetes&lt;br /&gt;
| Raised blood sugar level&lt;br /&gt;
|-&lt;br /&gt;
!Osteoporosis, muscle wasting and weakenss&lt;br /&gt;
| which is a danger, particularly in the elderly, as it can result in osteoporotic fractures for example of the hip or vertebrae&lt;br /&gt;
|-&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=412</id>
		<title>Fludrocortisone</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=412"/>
		<updated>2020-09-05T11:22:02Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
== Introduction ==&lt;br /&gt;
&lt;br /&gt;
Fludrocortisone is a steroid with potent mineralocorticoid activity. &lt;br /&gt;
It is used to treat:&lt;br /&gt;
*adrenocortical insufficiency&lt;br /&gt;
*postural hypotension&lt;br /&gt;
*adrenogenital syndrome&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Generic Name&lt;br /&gt;
!HA Code&lt;br /&gt;
!Legal Classification&lt;br /&gt;
|-&lt;br /&gt;
|Fludrocortisone Acetate Tablet 100mcg&lt;br /&gt;
|FLUD01&lt;br /&gt;
|P1S1S3&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Brand Name&lt;br /&gt;
!HK Reg Number&lt;br /&gt;
!Active Ingredients&lt;br /&gt;
|-&lt;br /&gt;
|FLORINEF TABLET 0.1mg&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|HK-00036&lt;br /&gt;
|fludrocortisone acetate&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Fludrocortisone is a corticosteroid with glucocorticoid and highly potent mineralocorticoid activity.&lt;br /&gt;
&lt;br /&gt;
== Dosage ==&lt;br /&gt;
Fludrocortisone is used, usually with hydrocortisone, for replacement therapy in adrenocortical insufficiency. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Replacement therapy in adrenal insufficiency&lt;br /&gt;
| Oral: 50-300 micrograms daily &lt;br /&gt;
|-&lt;br /&gt;
! severe orthostatic hypotension&lt;br /&gt;
| Oral: 50-300 micrograms daily&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
It is also used ear drops in concentration of 0.1%.&lt;br /&gt;
== Side Effects ==&lt;br /&gt;
Fludrocortisone acetate has glucocorticoid actions about 10 times as potent as hydrocortisone and mineralocorticoid effects more than 100 times as potent. &lt;br /&gt;
Adverse effects are mainly those due to mineralocorticoid activity:&lt;br /&gt;
*sodium and water retention&lt;br /&gt;
*swelling due to fluid retention (oedema)&lt;br /&gt;
*hypertension&lt;br /&gt;
*increased excretion of potassium leading to hypokalaemia&lt;br /&gt;
*heart failure may be induced in susceptible patients&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=411</id>
		<title>Fludrocortisone</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=411"/>
		<updated>2020-09-05T11:19:53Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
== Introduction ==&lt;br /&gt;
&lt;br /&gt;
Fludrocortisone is a steroid with potent mineralocorticoid activity. &lt;br /&gt;
It is used to treat:&lt;br /&gt;
*adrenocortical insufficiency&lt;br /&gt;
*postural hypotension&lt;br /&gt;
*adrenogenital syndrome&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Generic Name&lt;br /&gt;
!HA Code&lt;br /&gt;
!Legal Classification&lt;br /&gt;
|-&lt;br /&gt;
|Fludrocortisone Acetate Tablet 100mcg&lt;br /&gt;
|FLUD01&lt;br /&gt;
|P1S1S3&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Brand Name&lt;br /&gt;
!HK Reg Number&lt;br /&gt;
!Active Ingredients&lt;br /&gt;
|-&lt;br /&gt;
|FLORINEF TABLET 0.1mg&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|HK-00036&lt;br /&gt;
|fludrocortisone acetate&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Fludrocortisone is a corticosteroid with glucocorticoid and highly potent mineralocorticoid activity.&lt;br /&gt;
&lt;br /&gt;
== Dosage ==&lt;br /&gt;
Fludrocortisone is used, usually with hydrocortisone, for replacement therapy in adrenocortical insufficiency. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Replacement therapy in adrenal insufficiency&lt;br /&gt;
| Oral: 50-300 micrograms daily &lt;br /&gt;
|-&lt;br /&gt;
! severe orthostatic hypotension&lt;br /&gt;
| Oral: 50-300 micrograms daily&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
It is also used ear drops in concentration of 0.1%.&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=410</id>
		<title>Fludrocortisone</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=410"/>
		<updated>2020-09-05T11:18:56Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
== Introduction ==&lt;br /&gt;
&lt;br /&gt;
Fludrocortisone is a steroid with potent mineralocorticoid activity. &lt;br /&gt;
It is used to treat:&lt;br /&gt;
*adrenocortical insufficiency&lt;br /&gt;
*postural hypotension&lt;br /&gt;
*adrenogenital syndrome&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Generic Name&lt;br /&gt;
!HA Code&lt;br /&gt;
!Legal Classification&lt;br /&gt;
|-&lt;br /&gt;
|Fludrocortisone Acetate Tablet 100mcg&lt;br /&gt;
|FLUD01&lt;br /&gt;
|P1S1S3&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Brand Name&lt;br /&gt;
!HK Reg Number&lt;br /&gt;
!Active Ingredients&lt;br /&gt;
|-&lt;br /&gt;
|FLORINEF TABLET 0.1mg&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|HK-00036&lt;br /&gt;
|fludrocortisone acetate&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Fludrocortisone is a corticosteroid with glucocorticoid and highly potent mineralocorticoid activity.&lt;br /&gt;
&lt;br /&gt;
== Dosage ==&lt;br /&gt;
Fludrocortisone is used, usually with hydrocortisone, for replacement therapy in adrenocortical insufficiency. &lt;br /&gt;
{| class = &amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Replacement therapy in adrenal insufficiency&lt;br /&gt;
| Oral: 50-300 micrograms daily &lt;br /&gt;
! severe orthostatic hypotension&lt;br /&gt;
| Oral: 50-300 micrograms daily&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
It is also used ear drops in concentration of 0.1%.&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
	<entry>
		<id>https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=409</id>
		<title>Fludrocortisone</title>
		<link rel="alternate" type="text/html" href="https://www.sehk-wiki.org/index.php?title=Fludrocortisone&amp;diff=409"/>
		<updated>2020-09-05T11:04:15Z</updated>

		<summary type="html">&lt;p&gt;Annayung: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Category: Drugs]]&lt;br /&gt;
== Introduction ==&lt;br /&gt;
&lt;br /&gt;
Fludrocortisone is a steroid with potent mineralocorticoid activity. &lt;br /&gt;
It is used to treat:&lt;br /&gt;
*adrenocortical insufficiency&lt;br /&gt;
*postural hypotension&lt;br /&gt;
*adrenogenital syndrome&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Generic Name&lt;br /&gt;
!HA Code&lt;br /&gt;
!Legal Classification&lt;br /&gt;
|-&lt;br /&gt;
|Fludrocortisone Acetate Tablet 100mcg&lt;br /&gt;
|FLUD01&lt;br /&gt;
|P1S1S3&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
!Brand Name&lt;br /&gt;
!HK Reg Number&lt;br /&gt;
!Active Ingredients&lt;br /&gt;
|-&lt;br /&gt;
|FLORINEF TABLET 0.1mg&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
|HK-00036&lt;br /&gt;
|fludrocortisone acetate&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
== Mechanism of Action ==&lt;br /&gt;
Fludrocortisone is a corticosteroid with glucocorticoid and highly potent mineralocorticoid activity.&lt;br /&gt;
&lt;br /&gt;
== Dosage ==&lt;br /&gt;
Fludrocortisone is used, usually with hydrocortisone, for replacement therapy in adrenocortical insufficiency. &lt;br /&gt;
By Oral: as replacement therapy, 50-300 micrograms daily &lt;br /&gt;
It is also given in the management of severe orthostatic hypotension, but hypokalaemia, fluid retention and supine hypertension may limit its use. &lt;br /&gt;
It is used in eye ointment or ear drops in concentration of 0.1%.&lt;/div&gt;</summary>
		<author><name>Annayung</name></author>
	</entry>
</feed>