Sulpiride: Difference between revisions
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Most serious and/or frequently occurring adverse effects of sulpiride include the following: | Most serious and/or frequently occurring adverse effects of sulpiride include the following: | ||
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!Endocrine disorders | !style="text-align: left"| Endocrine disorders | ||
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*Common: hyperprolactinaemia (elevated plasma levels of the hormone prolactin, which in turn lead to galactonrrhea, amornorrhea, gynecomastia etc) | *Common: hyperprolactinaemia (elevated plasma levels of the hormone prolactin, which in turn lead to galactonrrhea, amornorrhea, gynecomastia etc) | ||
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!Nervous system | !style="text-align: left"| Nervous system | ||
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Common: | Common: | ||
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*Tardive dyskinesia | *Tardive dyskinesia | ||
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!Metabolism disorders | !style="text-align: left"| Metabolism disorders | ||
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Not known: | Not known: | ||
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*Syndrome of inappropriate antidiuretic hormone secretion (SIADH) | *Syndrome of inappropriate antidiuretic hormone secretion (SIADH) | ||
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!Cardiac disorders | !style="text-align: left"| Cardiac disorders | ||
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Rare: | Rare: | ||
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*Electrocardiogram QT prolonged | *Electrocardiogram QT prolonged | ||
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!Vascular disorder | !style="text-align: left"| Vascular disorder | ||
|Uncommon: orthostatic hypotension | |Uncommon: orthostatic hypotension | ||
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Uncommon: saliva hypersecretion | Uncommon: saliva hypersecretion | ||
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!Breast disorder | !style="text-align: left"| Breast disorder | ||
|Common: breast pain, galactorrhoea | |Common: breast pain, galactorrhoea | ||
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Common: | Common: | ||
*weight gain | *weight gain | ||
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==Pharmacokinetics== | |||
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!style="text-align: left"| Oral bioavailability | |||
|Sulpiride is readily absorbed after oral doses. | |||
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!style="text-align: left"| Onset of action | |||
|Peak plasma concentrations are reached 3 – 6 hours after an oral dose. | |||
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!style="text-align: left"| Metabolism | |||
|It is metabolized in the liver | |||
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!style="text-align: left"| Elimination half-life | |||
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It is excreted in the urine and faeces. | |||
The elimination half-life is approximately 8 hours. | |||
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Revision as of 23:15, 26 October 2020
Drug Class: Antipsychotics, typical ; Antipsychotics, 1st Generation Sulpiride (中文:[[ ]])is a typical antipsychotic or 1st Generation antipsychotic medication. It is used in the treatment of psychosis associated with schizophrenia and major depressive disorder. In low dosage, it is used for anxiety and mild depression.
Pronunciation
Sulpiride 200mg
Sulpiride 50mg
Drug Names
| Generic Name 藥名 | HA Code 藥物代碼 | Classification藥物分類 |
|---|---|---|
| Sulpiride Cap 50 mg | SULP19 | P1S1S3 |
| Sulpiride Tab 200 mg | SULP20 | P1S1S3 |
Mechanism of Action
Sulpiride is a selective antagonist at dopamine D2, D3 and 5-HT1A receptors. The presumed effectiveness of antipsychotic drugs relied on their ability to block dopamine receptors. This assumption arose from the dopamine hypothesis that maintains that both schizophrenia and bipolar disorder are a result of excessive dopamine activity.
Dosage
| Indication | Dose |
|---|---|
|
Schizophrenia with predominantly negative symptoms(flattening of affect, poverty of speech, apathy, as well as depression) |
By mouth
ADULT:
ELDERLY or debilitated patients:
|
|
Schizophrenia with mainly positive symptoms(hallucinations, delusions, incongruity of speech) Respond to higher doses |
By mouth
ADULT:
ELDERLY or debilitated patients:
|
Side Effects
Most serious and/or frequently occurring adverse effects of sulpiride include the following:
| Endocrine disorders |
|
|---|---|
| Nervous system |
Common:
-Tremor -Akathisia – a sense of inner restlessness that cannot stay still -Parkinsonism
-Dry mouth -Constipation -Blurred vision Uncommon:
Rare:
Not known:
|
| Metabolism disorders |
Not known:
|
| Cardiac disorders |
Rare:
Not known:
|
| Vascular disorder | Uncommon: orthostatic hypotension |
| Gastrointestinal disorder |
Common: constipation Uncommon: saliva hypersecretion |
| Breast disorder | Common: breast pain, galactorrhoea |
|
Common:
|
Pharmacokinetics
| Oral bioavailability | Sulpiride is readily absorbed after oral doses. |
|---|---|
| Onset of action | Peak plasma concentrations are reached 3 – 6 hours after an oral dose. |
| Metabolism | It is metabolized in the liver |
| Elimination half-life |
It is excreted in the urine and faeces. The elimination half-life is approximately 8 hours. |
