Drug Guide
Flurazepam Hydrochloride
Classification
Therapeutic: Sedative-Hypnotic, Anxiolytic
Pharmacological: Benzodiazepine
FDA Approved Indications
- Short-term management of insomnia characterized by difficulty with sleep initiation, duration, or both
Mechanism of Action
Enhances the effect of gamma-aminobutyric acid (GABA) at the GABA-A receptor, producing sedative, hypnotic, anxiolytic, anticonvulsant, and muscle relaxant properties.
Dosage and Administration
Adult: Initially, 30 mg at bedtime. Dose may be increased gradually up to 60 mg.
Pediatric: Not recommended for pediatric use.
Geriatric: Start at lower dose, typically 15 mg, with caution due to increased sensitivity and risk of side effects.
Renal Impairment: Use with caution; consult labeling for specific adjustments.
Hepatic Impairment: Use with caution; dose adjustment may be necessary.
Pharmacokinetics
Absorption: Well absorbed orally.
Distribution: Widely distributed; crosses the blood-brain barrier.
Metabolism: Metabolized in the liver mainly by CYP3A4 enzyme to active and inactive metabolites.
Excretion: Excreted primarily in urine as metabolites.
Half Life: Approximately 40-100 hours, contributing to its long duration of action.
Contraindications
- Hypersensitivity to benzodiazepines or any component of the formulation.
- Acute narrow-angle glaucoma.
Precautions
- Use with caution in elderly patients, patients with a history of substance abuse, respiratory impairment, hepatic impairment, or psychiatric disorders.
Adverse Reactions - Common
- Drowsiness (Common)
- Dizziness (Common)
- Gastrointestinal disturbances (Less common)
Adverse Reactions - Serious
- Respiratory depression (Rare)
- Dependence or abuse potential (Potential with prolonged use)
- Anterograde amnesia (Reported but uncommon)
Drug-Drug Interactions
- CNS depressants (alcohol, opioids, other sedatives) - increased sedative effects, risk of respiratory depression.
- Rifampin - decreased sedative effect due to increased metabolism.
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor for effectiveness in improving sleep, assess for signs of dependence, and observe for adverse reactions.
Diagnoses:
- Risk for falls due to sedation, dizziness, or impaired coordination.
- Risk for dependence with prolonged use.
Implementation: Administer at bedtime, instruct patient on proper use, and evaluate sleep patterns.
Evaluation: Effective sleep induction and maintenance without significant adverse effects or dependence.
Patient/Family Teaching
- Take medication exactly as prescribed, usually at bedtime.
- Avoid alcohol and other CNS depressants.
- Do not abruptly discontinue to prevent withdrawal symptoms.
- Use caution when rising from bed to prevent falls.
Special Considerations
Black Box Warnings:
- Potential for abuse and dependence.
- Risks from concomitant use with opioids.
Genetic Factors: Genetic variations in CYP3A4 may affect metabolism.
Lab Test Interference: None known.
Overdose Management
Signs/Symptoms: Excessive sedation, confusion, respiratory depression, coma.
Treatment: Supportive care, airway management, possible use of flumazenil as an antidote to reverse benzodiazepine effects under careful medical supervision.
Storage and Handling
Storage: Store at room temperature away from moisture, heat, and light.
Stability: Stable when stored properly, check expiration date.