Chlorpromazine

From SEHK Wiki

Chlorpromazine (中文:氯丙嗪) 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
  • 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

Intractable hiccup By mouth

ADULT: 25 – 50 mg 3-4 times a day

Nausea and vomiting of terminal illness By mouth

ADULT: 10 – 25 mg every 4-6 hours CHILD 1-5 years: 500 micrograms/kg every 4-6 hours; max. 40 mg per day CHILD 6-11 years: 500 micrograms/kg every 4-6 hours; max. 75 mg per day CHILD 12-17 years: 10 – 25 mg every 4-6 hours By rectum ADULT: 100 mg every 6-8 hours

Chlorpromazine is given orally as the hydrochloride and the embonate.

For both salts, the doses are expressed as the hydrochloride. Chlorpromazine embonate 144 mg is equivalent to 100 mg of chlorpromazine hydrochloride.

If the oral route is not suitable, it may be given rectally as suppositories containing 100 mg of chlorpromazine base

Side Effects

Chlorpromazine generally produces less central depression than the benzodiazepines, and tolerance to its initial sedative effects develops quickly in most patients. Tardive dyskinesia (involuntary, repetitive body movements) and akathisia (a feeling of inner restlessness and inability to stay still) are less commonly seen with chlorpromazine than they are with high potency typical antipsychotics such as haloperidol or trifluoperazine.

Possible side effects include:

It has antimuscarinic properties and may cause the following side effects such as
  • Dry mouth
  • Constipation
  • Difficulty to urinate
  • Blurred vision
  • Mydriasis
  • Tachycardia
  • ECG changes (particularly Q- and T-wave abnormalities)
  • Orthostatic hypotension is common
Other adverse effects include
  • Delirium
  • Agitation
  • sedation
  • Insomnia
  • Nightmares
  • Glaucoma
  • Inhibition of ejaculation
  • Impotence
Hypersensitivity reactions include
  • Urticaria
  • Exfoliative dermatitis
  • Prolonged therapy may lead to deposition of pigment, producing a bluish-purple discoloration in the skin
  • Corneal and lens opacities
  • Photosensitivity reaction
Haematological disorders
  • Haemolytic anaemia
  • Thrombocytopenic purpura
  • Most cases of agranulocytosis occurred within 4 to 10 weeks starting treatment
Extrapyramidal dysfunction include
  • Acute dystonia
  • A parkinsonism-like syndrome
  • Tardive dyskinesia
  • Neuroleptic malignant syndrome
Altered endocrine and metabolic functions
  • Developed amenorrhoea, galactorrhoea and gynaecomastia due to hyperprolactinaemia
  • Weight gain
  • Hyperglycaemia
  • Body temperature regulation is impaired and may result in hypo- or hyperthermia depending on environment.

Pharmacokinetics

Oral bioavailability Chlorpromazine is readily, although sometimes erratically absorbed after oral doses.
Onset of action Peak plasma concentrations occur about 2 to 4 hours after ingestion.
Metabolism It is subject to considerable first-pass metabolism in the gut wall and is also extensively metabolized in the liver.
Elimination half-life

It is excreted in the urine and faeces. Owing to the first-pass effect, plasma concentrations after oral doses are much lower than those after intramuscular doses. The plasma half-life of chlorpromazine occurs about 30 hours.

Drug Management

=onitoring

The following populations must be closely monitored after administration of chlorpromazine:

  • Epileptics, since chlorpromazine may lower the seizure threshold. Treatment must be stopped if seizures occur.
  • Elderly persons with susceptibility to orthostatic hypotension, sedation, and extrapyramidal effects; chronic constipation and prostatic hypertrophy.
  • Patients with cardiovascular disease since chlorpromazine can induce tachycardia and hypotension. Regular BP and pulse monitoring are recommended.
  • Patients with severe liver and/or renal failure because of the risk of accumulation.
  • Patients on long-term treatment should receive regular eye examinations.
  • Diabetic patients who are started on chlorpromazine should get glycemic monitoring during treatment.
  • Chlorpromazine commonly causes increased susceptibility to sunburn and individuals should avoid undue exposure to direct sunlight.
  • Chlorpromazine impairs body temperature regulation. The elderly or hypothyroid patient may be particularly susceptible to hypothermia. The hazard of hyperthermia may be increased by hot weather.

Drug interaction

The most common interactions encountered with chlorpromazine result from use with drugs that have similar pharmacological actions

Drugs given with chlorpromazine Potential Effect
  • CNS-depressant drugs including alcohol, hypnotics, anxiolytics, and opioids.
Potentiates the sedative effect.
  • Lithium
Concomitant use can cause confusion, with a rapid increase in serum lithium.
  • Drugs with antimuscarinic actions such as tricyclic antidepressants
As chlorpromazine has antimuscarinic actions, they can potentiate the adverse effects.
  • Antiparkinsonian drugs (amantadine, bromocriptine, levodopa, ropinirole)
In theory, antipsychotics with dopamine-blocking activity and dopaminergic drugs such as those used to treat parkinsonism may be mutually antagonistic.
  • metoclopramide
May increase the risk of antipsychotic-induced extrapyramidal effects.
  • Drugs that prolong the QT interval e.g. amiodarone, verapamil, sotalol and quinidine
An increased risk of ventricular arrhythmias – avoid concomitant use.
  • Antacids (magnesium, aluminum and calcium salts, oxides and hydroxides)
Decreased GI absorption of chlorpromazine. Administer chlorpromazine and antacid more than 2 hours apart if possible.

Caution

  • In patients with impaired liver, kidney, cardiovascular and respiratory function
  • In those with angle-closure glaucoma
  • In patients with a history of jaundice, parkinsonism
  • In those with diabetes mellitus, hypothyroidism
  • In patients with myasthenia gravis, paralytic ileus
  • In patients with prostatic hyperplasia or urinary retention
  • Care is required in patients with epilepsy
  • Debilitated patients, the elderly, especially those with dementia.

Contra-indications

Use of chlorpromazine should be avoided in individuals with:

  • CNS depression or coma
  • Bone-marrow suppression
  • Pheochromocytoma (tumour of the adrenal gland)

Hepatic impairment

  • Chlorpromazine is hepatotoxic
  • Can precipitate coma.

Renal impairment

  • Start with small doses in severe impairment.

Handling and Storage Owing to the risk of contact sensitization, pharmacists, nurses and other health workers should avoid direct contact with chlorpromazine; tablets should not be crushed.

Pregnancy

Should be avoided in pregnancy unless the physician considers it essential.

Breast-feeding

Use during breast feeding is not recommended.

Driving and skilled tasks

Drivers and machine operators should be told about the risk of drowsiness with this medication especially at the start of treatment. Affected patients should not drive or operate machinery.

FAQ

How should I take the tablet?

You will be prescribed the lowest dose needed to control your symptoms. Do not stop taking chlorpromazine suddenly, or you could have unpleasant withdrawal symptoms. The tablet should be swallowed with a glass of water.

What should I avoid while taking?

Avoid drinking alcohol while taking chlorpromazine because it may enhance the side effects of sedation.

Avoid driving or hazardous activity until you know how chlorpromazine will affect you.

Avoid getting up too fast from a sitting or lying position, or you may feel dizzy.

Avoid exposure to sunlight or tanning beds. Chlorpromazine can make you sunburn more easily. Wear protective clothing and use sunscreen (SPF 30 or higher) when you are outdoors.

What happen if I overdose?

Contact your primary care doctor. If emergency situation, call 999

What happen if I miss a dose?

Take it as soon as you remember. If it is near the time of the next dose, skip the missed dose. Take your next dose at the regular time. Do not double the dose to catch up.