Drug Guide
Chlorpromazine Hydrochloride
Classification
Therapeutic: Antipsychotic (neuroleptic)
Pharmacological: Phenothiazine antipsychotic
FDA Approved Indications
- Schizophrenia
- Manic phases of bipolar disorder
- ^Prevention of nausea and vomiting
- ^Preoperative sedation
Mechanism of Action
Chlorpromazine acts by antagonizing dopamine D2 receptors in the central nervous system, leading to a decrease in dopaminergic neurotransmission, which alleviates psychotic symptoms.
Dosage and Administration
Adult: Initial dose: 25-50 mg 3-4 times daily; dosage can be adjusted based on response and tolerability.
Pediatric: Use is limited; consult specialist. Typical doses are 0.2 mg/kg/day divided into two or three doses.
Geriatric: Start at a lower dose, e.g., 25 mg/day, and titrate slowly.
Renal Impairment: Adjust dose based on clinical response and tolerability.
Hepatic Impairment: Use with caution; close monitoring recommended.
Pharmacokinetics
Absorption: Well absorbed orally.
Distribution: Widely distributed in body tissues; crosses the blood-brain barrier and placental barrier.
Metabolism: Primarily hepatic via CYP450 enzymes.
Excretion: Metabolites excreted in urine; unchanged drug minimally excreted in urine.
Half Life: Approximately 10-20 hours, varies with individual.
Contraindications
- Coma, CNS depression, hypersensitivity to phenothiazines.
Precautions
- Use with caution in patients with cardiovascular disease, Parkinson's disease, liver impairment, or a history of seizure disorders.
- Pregnancy Category C; use only if potential benefit justifies risk. Lactation: use cautiously.
Adverse Reactions - Common
- Sedation, dizziness (Common)
- Dry mouth (Common)
- Orthostatic hypotension (Common)
Adverse Reactions - Serious
- Extrapyramidal symptoms (dystonia, Parkinsonism, akathisia) (Less common)
- Neuroleptic malignant syndrome (Rare)
- Prolonged QT interval, cardiac arrhythmias (Rare)
- Agranulocytosis (Rare)
Drug-Drug Interactions
- CNS depressants (enhanced sedation)
- Anticholinergic drugs (additive side effects)
- Agents prolonging QT interval (risk of arrhythmias)
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor mental status, cardiac function (ECG), blood counts, and EPS symptoms.
Diagnoses:
- Risk for falls due to sedation or orthostatic hypotension.
- Risk for injury from extrapyramidal symptoms.
Implementation: Administer with food to minimize GI upset. Educate patient on orthostatic precautions.
Evaluation: Assess symptom improvement and monitor for adverse effects.
Patient/Family Teaching
- Take medication exactly as prescribed.
- Change positions slowly to prevent dizziness.
- Report any signs of EPS, fever, sore throat, or signs of allergic reactions.
- Avoid alcohol and CNS depressants.
Special Considerations
Black Box Warnings:
- Elderly patients with dementia-related psychosis treated with antipsychotics are at increased risk of death.
Genetic Factors: CYP2D6 poor metabolizers may have increased drug levels.
Lab Test Interference: May cause false-positive for catecholamine levels.
Overdose Management
Signs/Symptoms: Sedation, hypotension, extrapyramidal symptoms, coma, seizures.
Treatment: Supportive care; monitor vital signs; activated charcoal if ingestion recent; saline IV; for severe reactions, consider specific antidotes and intensive supportive measures.
Storage and Handling
Storage: Store at room temperature, 20-25°C (68-77°F).
Stability: Stable under proper conditions, check manufacturer label for specific details.