Drug Guide
Haloperidol Decanoate
Classification
Therapeutic: Antipsychotic, typical (first-generation)
Pharmacological: Dopamine D2 receptor antagonist
FDA Approved Indications
- Schizophrenia
- Schizoaffective disorder (maintenance treatment)
Mechanism of Action
Blocks dopamine D2 receptors in the brain, reducing psychotic symptoms.
Dosage and Administration
Adult: Typically administered every 4 weeks via intramuscular injection, dose varies based on patient response and prior therapy.
Pediatric: Not FDA-approved for pediatric use; off-label use under certain circumstances with caution.
Geriatric: Use with caution due to increased sensitivity to side effects; dosing adjustments are common.
Renal Impairment: No specific adjustment necessary, but monitor response.
Hepatic Impairment: Use with caution; no specific adjustments established.
Pharmacokinetics
Absorption: Slowly absorbed after intramuscular injection.
Distribution: Widely distributed in tissues, crosses blood-brain barrier.
Metabolism: Metabolized in the liver via CYP3A4.
Excretion: Excreted primarily in urine as metabolites.
Half Life: Approximately 3 weeks (very long-acting depot formulation).
Contraindications
- Coma
- Pts with Parkinson's disease
- Historically hypersensitive to haloperidol or other butyrophenones.
Precautions
- Use cautiously in elderly with dementia-related psychosis; risk of mortality.
- Monitor for neuroleptic malignant syndrome, extrapyramidal symptoms, tardive dyskinesia.
- Pregnancy category C; benefits vs risks should be considered.
Adverse Reactions - Common
- Extrapyramidal symptoms (EPS) (Common)
- Sedation (Common)
- Weight gain (Less common)
Adverse Reactions - Serious
- Neuroleptic malignant syndrome (NMS) (Rare)
- QT prolongation and arrhythmias (Rare)
- Tardive dyskinesia (Rare)
Drug-Drug Interactions
- CNS depressants
- Other dopamine antagonists (antipsychotics, metoclopramide)
- QT prolonging agents (amiodarone, certain antibiotics)
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor mental status, motor and neurological side effects, cardiac status, and vital signs.
Diagnoses:
- Risk for injury (due to EPS or sedation)
- Imbalanced nutrition: less than body requirements
Implementation: Administer injection deep into gluteal muscle; monitor for side effects; adjust dose as needed.
Evaluation: Assess for symptom control, adverse effects, and adherence.
Patient/Family Teaching
- Report any involuntary movements, fever, muscle rigidity, or unusual tiredness.
- Take medication as prescribed, even if feeling well.
- Avoid alcohol and other CNS depressants.
- Be aware of potential side effects and when to seek medical help.
Special Considerations
Black Box Warnings:
- Increased mortality in elderly patients with dementia-related psychosis.
- QT interval prolongation, which can lead to serious arrhythmias.
Genetic Factors: Metabolism may vary with CYP2D6 polymorphisms.
Lab Test Interference: May cause false positives in certain drug screens.
Overdose Management
Signs/Symptoms: Drowsiness, agitation, extrapyramidal symptoms, hypotension, seizures, coma.
Treatment: Supportive care, monitor cardiac function, manage symptoms, consider activated charcoal if recent ingestion, and specific interventions for complications.
Storage and Handling
Storage: Store at room temperature, protected from light and moisture.
Stability: Stable under proper storage conditions.