Brand Name: Thorazine, Largactil

Chlorpromazine Hydrochloride is an Antipsychotic Medication used to treat psychotic disorders such as schizophrenia and manic depressive illness. Detailed info on uses, dosage and side-effects of Chlorpromazine below.

Contents:

Description
Pharmacology
Indications and Usage
Contraindications
Warnings
Precautions
Drug Interactions
Adverse Reactions
Overdose
Dosage

Description

Chlorpromazine (Thorazine, Largactil) is a phenothiazine used to treat emotional disorders such as schizophrenia, nausea, vomiting, severe pain, and continuous hiccups. It may also be used to treat other conditions as determined by your doctor.

Pharmacology

Chlorpromazine is an aliphatic phenothiazine. Phenothiazines are thought to elicit their antipsychotic and antiemetic effects via interference with central dopaminergic pathways in the mesolimbic and medullary chemoreceptor trigger zone areas of the brain, respectively. Extrapyramidal side effects are a result of interaction with dopaminergic pathways in the basal ganglia. Although often termed dopamine blockers, the exact mechanism of dopaminergic interference responsible for the drugs antipsychotic activity has not been determined.

The aliphatic phenothiazines are highly sedating which is often apparent at the start of therapy; with time some tolerance to this effect develops. Chlorpromazine has strong alpha-adrenergic blocking activity and can cause orthostatic hypotension. Infrequently prolongation of the QT interval may occur. Chlorpromazine has moderate anticholinergic activity manifested as occasional dry mouth, blurred vision, urinary retention and constipation.

Chlorpromazine increases prolactin secretion due to its dopamine receptor blocking action in the pituitary and hypothalamus. Galactorrhea and gynecomastia have occurred.

Indications and Usage

The management of psychotic disorders including manifestations of manic depressive illness, manic phase and severe behavioral problems in children; nausea and vomiting due to stimulation of the chemoreceptor trigger zone.

Contraindications

Comatose or depressed states due to CNS depressants; blood dyscrasias; bone marrow depression; liver damage. Hypersensitivity to chlorpromazine. Cross allergenicity with other phenothiazines may occur.

Should be avoided in children or adolescents with signs or symptoms suggestive of Reye's Syndrome. Its antiemetic effect may mask the signs and its CNS effect may be confused with the signs of Reye's Syndrome or other encephalopathies.

Warnings

Phenothiazines should be used with caution in patients with cardiovascular disease. Chlorpromazine is an alpha-adrenergic blocking agent and increased pulse rate and transient hypotension have both been reported in some patients receiving these drugs.

Hypotension may occur, especially in elderly and in alcoholic patients. This effect may be additive with other agents that cause a lowering of blood pressure. If chlorpromazine should cause severe hypotension, most patients will respond to cautious expansion of the intravascular volume with sodium chloride. If vasopressor drugs are needed, the drugs of choice are alpha-receptor agonists such as phenylephrine or methoxamine.

Use chlorpromazine cautiously in patients with a history of seizures since the drug tends to lower the seizure threshold.

Chlorpromazine should be used with caution in patients who have impaired liver function or alcoholic liver disease. CNS depression may be potentiated.

If bilirubinemia, or icterus occur, discontinue the drug and perform liver function tests.

Phenothiazines have been associated with retinopathy. Discontinue chlorpromazine if retinal changes are observed. Regular ophthalmologic exams are recommended.

Chlorpromazine may mask signs of overdosage of toxic drugs and may obscure conditions such as intestinal obstruction and brain tumor.

Neuroleptic drugs elevate prolactin levels; the elevation persists during chronic administration. Although disturbances such as galactorrhea, amenorrhea, gynecomastia, and impotence have been reported, the clinical significance of elevated serum prolactin levels is unknown for most patients.

Usage in Pregnancy & Nursing

Safe use of phenothiazines in pregnancy has not been established. Most studies indicate these agents are not teratogenic but there are reports of defects in infants exposed to these drugs during the first trimester. Toxic effects observed after high doses near term include: hypotonia, lethargy, depressed reflexes, paralytic ileus, jaundice, and persistent extrapyramidal syndrome. Therefore, they should be administered cautiously to women of childbearing potential particularly during the first trimester of pregnancy and near term.

Phenothiazines are distributed into milk. Use with caution during lactation because of possible sedative and anticholinergic side effects on the infant.

Elderly: Use reduced dosages. Chlorpromazine may adversely affect many of the conditions commonly occurring in the aged, including cardiovascular problems, parkinsonian extrapyramidal effects and anticholinergic effects (e.g. constipation, blurred vision).

Precautions

Dependence and Withdrawal: In general, phenothiazines do not produce psychic dependence; however, gastritis, nausea and vomiting, dizziness, and tremulousness have been reported following abrupt cessation of high dose therapy. Reports suggest that these symptoms can be reduced if concomitant antiparkinsonian agents are continued for several weeks after the phenothiazine is withdrawn.

Interference with cognitive and motor performance: Where patients are participating in activities requiring complete mental alertness such as driving an automobile or operating machinery, administer the phenothiazine cautiously, forewarn the patient and increase the dosage gradually.

Photosensitivity may occur. Patients should utilize sunscreens when exposed to sunlight for significant lengths of time.

Drug Interactions

Alcohol: Additive CNS depressant effects.

Amphetamines: Amphetamines may cause exacerbation of psychotic symptoms.

Anticonvulsants: Chlorpromazine may lower the seizure threshold. Anticonvulsant therapy should be monitored closely and may require dosage adjustment. May impair the absorption of chlorpromazine. Monitor for decreased effect.

Antidepressants, tricyclic: May result in increased chlorpromazine concentration, monitor for adverse effects.

CNS Depressants: Chlorpromazine and other CNS depressants (alcohol, antihistamines, general anesthetics, opiates or other narcotic analgesics, barbiturates, benzodiazepines and other sedative/hypnotic agents) may result in additive CNS depressant effects. Monitor to avoid excessive sedation or respiratory depression.

Hypotensive Agents: Chlorpromazine and antihypertensives may result in additive hypotensive effects and increased risk of orthostatic hypotension or syncope (fainting). Chlorpromazine may block the antihypertensive effects of guanethidine by preventing its uptake into sympathetic nerves.

Levodopa: Phenothiazines may inhibit the antiparkinsonian effects of levodopa due to their dopamine blocking effects in the CNS. Generally, phenothiazines should not be administered to patients who require levodopa.

Lithium: Patients receiving lithium and chlorpromazine for treatment of acute mania should be monitored closely for signs of adverse neurologic effects, especially if serum concentrations of lithium are in the upper range. Rare cases of severe neurotoxicity have been reported.

BEFORE USING THIS MEDICINE: INFORM YOUR DOCTOR OR PHARMACIST of all prescription and over-the-counter medicine that you are taking. This includes meperidine, diazoxide, guanethidine, medicines used to treat high blood pressure and heart conditions, medicines used to treat depression, and medicines used to treat bladder or bowel spasms. Inform your doctor of any other medical conditions including seizure disorders, depression, allergies, pregnancy, or breast-feeding.

Adverse Reactions

CHECK WITH YOUR DOCTOR AS SOON AS POSSIBLE if you experience changes in vision; changes in breasts; changes in menstrual period; sore throat; inability to move eyes; muscle spasms of face, neck, or back; difficulty swallowing; mask-like face; tremors of hands; restlessness; tension in legs; shuffling walk or stiff arms or legs; puffing of cheeks; lip smacking or puckering; twitching or twisting movements; or weakness of arms or legs.

Do not become overheated in hot weather, during exercise, or other activities since heat stroke may occur while you are using this medicine. This medicine may cause increased sensitivity to the sun. Avoid exposure to the sun or sunlamps until you know how you react to this medicine. Use a sunscreen or protective clothing if you must be outside for a prolonged period.

In general, members of the aliphatic group of phenothiazines have strong sedative, hypotensive and anticholinergic properties and mild to moderate extrapyramidal effects.

Automatic Nervous System: Anticholinergic effects including dry mouth, blurred vision, constipation, ileus, nasal stuffiness, photophobia. Syncope and impaired temperature regulation have also occurred.

Cardiovascular: Chlorpromazine has peripheral alpha-adrenergic blocking activity. Its effects on the heart include: direct negative inotropic and quinidine-like actions. Its effects on the ECG include prolongation of the PR and QT intervals, blunting of the T wave and depression of the S-T segment. Ventricular arrythmia and sudden death have occurred rarely.

Orthostatic hypotension is common after parenteral administration and usually lasts one-half to 2 hours. Patients should be supine when parenteral chlorpromazine is administered. Tachycardia, fainting and dizziness have also occurred. Hypotension can also occur after oral administration. Tolerance to hypotensive effects generally develop over time, however hypotension can persist in some patients, especially the elderly.

Central Nervous System: Extrapyramidal reactions, including pseudoparkinsonism (with motor retardation, rigidity, mask like facies, pill rolling and other tremors, drooling, shuffling gait, etc.); dystonic reactions (including periroral spasms, trismus, tics, torticollis, oculogyric crises, protrusion of the tongue, difficulty swallowing, carpopedal spasm, opisthotonos of the back muscles); and akathisia. In addition, slowing of the EEG rhythm, disturbed body temperature and lowering of the convulsive threshold have occurred. Dizziness has been reported.

Tardive dyskinesia may appear in some patients on long term antipsychotic therapy or may appear after drug therapy has been discontinued. The risk appears to be greater in elderly patients on high-dose therapy, especially females. The symptoms are persistent and in some patients appear to be irreversible. The syndrome is characterized by rhythmical involuntary movements of the tongue, face, mouth or jaw (e.g. protrusion of the tongue, puffing of the cheeks, puckering of the mouth and chewing movements). Sometimes these may be accompanied by involuntary movements of the extremities.

There is no known effective treatment for tardive dyskinesia; antiparkinsonian agents usually do not alleviate the symptoms of this syndrome. All antipsychotic agents should be discontinued if these symptoms appear. Should it be necessary to reinstitute treatment, or increase the dosage of the agent, or switch to a different antipsychotic agent, the syndrome may be masked. The physician may be able to reduce the risk of this syndrome by minimizing the unnecessary use of neuroleptics and reducing the dose or discontinuing the drug, if possible, when manifestations of this syndrome are recognized, particularly in patients over the age of 50. Fine vermicular movements of the tongue may be an early sign of the syndrome. If the medication is stopped at that time, the syndrome may not develop.

Dermatologic: Itching, rash, hypertrophic papillae of the tongue, angioneurotic edema, erythema, allergic purpura, exfoliative dermatitis, photosensitivity. Contact dermatitis has occurred in personnel handling solutions or injections of chlorpromazine.

Endocrine: Increased prolactin secretion; gynecomastia, galactorrhea, mastalgia, altered libido, menstrual irregularities, weight gain, alterations in glucose tolerance and false positive pregnancy tests have occurred.

Gastrointestinal: Nausea, vomiting, increase or decrease in appetite, gastric irritation, constipation, paralytic ileus, rarely diarrhea. Dry mouth.

Genitourinary: Urinary retention, priapism, inhibition of ejaculation.

Hematologic: Agranulocytosis, leukopenia, granulocytopenia, eosinophilia, thrombocytopenia, anemia, aplastic anemia, pancytopenia. Agranulocytosis occurs in fewer than 1 in 10000 patients receiving chlorpromazine.

Hepatic:: Cholestatic jaundice can occur infrequently (0.1-4%) and is usually part of a hypersensitivity reaction. Jaundice usually occurs within 2 to 4 weeks of initiation of therapy and chlorpromazine should be discontinued immediately. Rarely progression to chronic jaundice has occurred. Pre-existing liver dysfunction has not yet been proven to be a risk factor for this reaction. Signs and symptoms of cholestatic jaundice include; upper abdominal pain, nausea, flu-like symptoms, yellow skin and conjunctiva, fever, elevated liver enzymes, biliuria.

Hypersensitivity: Cholestatic jaundice (see under Hepatic), various dermatoses (see under Dermatologic), blood dyscrasias (see under Hematologic), photosensitivity, laryngeal edema, bronchospasm, angioneurotic edema and anaphylactoid reaction.

Ophthalmologic: A peculiar skin-eye syndrome has been recognized as an adverse effect following long-term treatment with phenothiazines. This reaction is marked by progressive pigmentation of areas of skin or conjunctiva and/or discoloration of the exposed sclera and cornea. Opacities of the anterior lens and cornea described as irregular or stellate in shape have also been reported. Patients receiving higher doses of phenothiazines for prolonged periods should have periodic complete eye examinations.

General Systemic Events: Sudden death has occasionally been reported in patients who have received phenothiazines. In some cases, the death was apparently due to cardiac arrest; in others, the cause appeared to be asphyxia due to failure of the cough reflex. In some patients, the cause could not be determined nor could it be established that the death was due to the phenothiazine.

Neuroleptic Malignant Syndrome: As with other neuroleptic drugs, a symptom complex sometimes referred to as neuroleptic malignant syndrome (NMS) has been reported. Cardinal features of NMS are hyperpyrexia, muscle rigidity, altered mental status (including catatonic signs) and evidence of autonomic instability (irregular pulse or unstable blood pressure). Additional signs may include elevated CPK, myoglobinuria (rhabdomyolysis), and acute renal failure. NMS is rare but potentially fatal and therefore requires intensive symptomatic and supportive treatment. Immediate discontinuation of neuroleptic treatment is mandatory. NMS has been successfully managed with various agents e.g. dantrolene and bromocriptine or amantadine. A toxicology reference should be consulted for detailed information.

Overdose

Signs and Symptoms

Parkinsonism, acute dystonias, somnolence, seizures, dry mouth, blurred vision, urinary retention, tachycardia, cardiac arrhythmias, hypotension, hypothermia or hyperthermia.

Symptoms of overdose may include restlessness, muscle spasms, tremors, twitching, deep sleep or loss of consciousness, and seizures.

Treatment

If you or someone you know may have used more than the recommended dose of this medicine, contact your local poison control center or emergency room immediately.

Empty stomach using gastric lavage. Administer activated charcoal and a saline cathartic. Repeat activated charcoal and cathartic every 4 to 6 hours to speed elimination. Support respiratory and cardiac functions as needed. Maintain fluid and electrolyte balance. Treat hypotension with i.v. fluids and by placing the patient in shock position. If unresponsive, dopamine may be required. Seizures may be treated with i.v. diazepam. Treat arrhythmias with phenytoin. Acute dystonic reactions may be treated with i.v. diphenydramine, benztropine or trihexyphenidyl. Hemodialysis is ineffective. Hemoperfusion may be effective in severe cases but is usually not necessary.

Dosage

Do not exceed the recommended dosage or take this medicine (Thorazine) for longer than prescribed. Exceeding the recommended dose or taking this medicine for longer than prescribed may be habit forming.

• Follow the directions for using this medicine provided by your doctor.
• Store this medicine at room temperature, in a tighly-closed container, away from heat and light.
• If you miss a dose of this medicine and you are using it regularly, take it as soon as possible. If you are taking 1 dose at bedtime and do not remember until the next morning, skip the missed dose and go back to your regular dosing schedule.

Additional Information:: Do not share this medicine with others for whom it was not prescribed. Do not use this medicine for other health conditions. Keep this medicine out of the reach of children.

For Adults: the average daily oral dose of 25 to 75 mg (mild cases) or 75 to 150 mg (more severe cases) in 2-4 divided doses. It is occasionally necessary to give a higher dosage which, when increased gradually, can reach 900 mg or more per day in some psychiatric patients. Optimum therapeutic response may not occur for weeks or months.

Once the optimum dosage has been reached, it is maintained as long as necessary for the control of symptoms during the critical phase of the illness. Eventually, however, it should be gradually reduced so that the patient can be maintained on the lowest effective dosage.

Elderly: Elderly and debilitated patients should start with initial doses at the lowest end of the dosage range (e.g. 25 mg daily). Such patients are more susceptible to hypotension and CNS effects and special caution should be exercised when using chlorpromazine in this age group.

During maintenance treatment, if it becomes desirable to reduce the number of daily drug administrations, the dosage may be administered once or twice daily, with the largest dose at bedtime.

Children: Oral: Usual single dose is 0.5 mg/kg. This dose may be repeated every 4 to 6 hours as necessary.

IF USING THIS MEDICINE FOR AN EXTENDED PERIOD OF TIME, obtain refills before your supply runs out.

NOTE:: This information is not intended to cover all possible uses, precautions, interactions, or adverse effects for this drug. If you have questions about the drug(s) you are taking, check with your health care professional.

The information in this monograph is not intended to cover all possible uses, directions, precautions, drug interactions or adverse effects. This information is generalized and is not intended as specific medical advice. If you have questions about the medicines you are taking or would like more information, check with your doctor, pharmacist, or nurse.

top . send to friend . medications homepage

Reviewed: 01/2006