Chlorpromazine: Difference between revisions
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*α1- and α2-adrenergic receptors accounting for lowering of blood pressure, reflex tachycardia, vertigo, sedation, hypersalivation and incontinence as well as sexual dysfunction | *α1- and α2-adrenergic receptors accounting for lowering of blood pressure, reflex tachycardia, vertigo, sedation, hypersalivation and incontinence as well as sexual dysfunction | ||
*M1 and M2 muscarinic acetylcholine receptors causing anticholinergic symptoms such as dry mouth, blurred vision, constipation, difficulty to urinate, sinus tachycardia, and loss of memory. | *M1 and M2 muscarinic acetylcholine receptors causing anticholinergic symptoms such as dry mouth, blurred vision, constipation, difficulty to urinate, sinus tachycardia, and loss of memory. | ||
==Dosage== | |||
{| class="wikitable" | |||
!style="text-align: left"| Indication | |||
!style="text-align: left"| Dose | |||
|- | |||
|style="text-align: left"| | |||
*Acute and chronic schizophrenia | |||
*Reduce acute mania in bipolar disorder | |||
*Control severely violent behaviour | |||
*Adjunctive management of severe anxiety | |||
|By ''mouth | |||
ADULT: | |||
*Initially 25 mg 3 times a day, adjusted according to response | |||
*Or initially 75 mg once daily, taken at night, adjusted according to response | |||
*Maintenance 75 – 300 mg daily | |||
ELDERLY or debilitated patients: | |||
*A third to half adult dose | |||
By ''rectum | |||
ADULT: 25 – 50 mg 3 – 4 times a day | |||
Revision as of 00:07, 14 October 2020
Chlorpromazine (中文:[[ ]]) is a typical antipsychotic medication. It is used to treat psychotic disorders such as
- schizophrenia
- Bipolar disorder
- Severe anxiety
- Attention deficit hyperactivity disorder
- Hiccups that do not improve following other measures
Pronunciation
Chlorpromazine 50mg
Drug Names
| Generic Name 藥名 | HA Code 藥物代碼 | Classification藥物分類 |
|---|---|---|
| Chlorpromazine Tablet 25 mg | CHLO44 | P1S1S3 |
| Chlorpromazine Tablet 50 mg | CHLO46 | P1S1S3 |
Mechanism of Action
Chlorpromazine and other typical antipsychotics are primarily blockers of D2 dopamine receptor. 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. In addition, chlorpromazine also acts as an antagonist (blocking agent) on different postsynaptic and presynaptic receptors:
- Dopamine receptors (subtypes D1, D2, D3 and D4), which account for its antipsychotic properties
- Serotonin receptors (5-HT2, 5-HT6 and 5-HT7), with anxiolytic, antidepressant, and anti-aggressive properties
- Histamine receptors (H1 receptors) accounting for sedation, antiemetic effect
- α1- and α2-adrenergic receptors accounting for lowering of blood pressure, reflex tachycardia, vertigo, sedation, hypersalivation and incontinence as well as sexual dysfunction
- M1 and M2 muscarinic acetylcholine receptors causing anticholinergic symptoms such as dry mouth, blurred vision, constipation, difficulty to urinate, sinus tachycardia, and loss of memory.
Dosage
| Indication | Dose |
|---|---|
|
By mouth
ADULT:
ELDERLY or debilitated patients:
By rectum ADULT: 25 – 50 mg 3 – 4 times a day |
