Drug Guide
Glutethimide
Classification
Therapeutic: Sedative, Hypnotic
Pharmacological: Central Nervous System depressant
FDA Approved Indications
- Short-term management of insomnia
Mechanism of Action
Glutethimide depresses the central nervous system by enhancing the action of gamma-aminobutyric acid (GABA) at GABA-A receptors, leading to sedative and hypnotic effects.
Dosage and Administration
Adult: Initial dose: 300 mg at bedtime; dose may be adjusted up to 900 mg per day in divided doses.
Pediatric: Not recommended due to lack of safety data.
Geriatric: Start with lower doses due to increased sensitivity and risk of adverse effects.
Renal Impairment: Use with caution; adjust dose if necessary based on renal function.
Hepatic Impairment: Use cautiously as hepatic metabolism may be impaired.
Pharmacokinetics
Absorption: Well absorbed orally.
Distribution: Widely distributed; crosses the blood-brain barrier.
Metabolism: Metabolized in the liver, primarily via hydroxylation and conjugation.
Excretion: Excreted in the urine as metabolites.
Half Life: Approximately 4-6 hours.
Contraindications
- Hypersensitivity to glutethimide or other sedative-hypnotics.
- History of substance abuse.
Precautions
- Use with caution in patients with respiratory disorders, hepatic or renal impairment, or a history of addiction.
- Monitor for development of dependence and withdrawal symptoms.
Adverse Reactions - Common
- Drowsiness, dizziness (Common)
- Nausea, vomiting (Less common)
Adverse Reactions - Serious
- Respiratory depression (Rare)
- Dependence and withdrawal symptoms (Rare)
- Psychoses, hallucinations (Rare)
Drug-Drug Interactions
- Other CNS depressants, including alcohol, opioids, and antihistamines (increased sedation)
- Cimetidine or other drugs affecting hepatic metabolism (altered glutethimide levels)
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor for sedation level, respiratory status, signs of dependence, and hepatic function.
Diagnoses:
- Risk of sedation-related falls
- Risk for dependence
Implementation: Administer at bedtime to reduce daytime sedation; gradually taper to discontinue.
Evaluation: Assess effectiveness for insomnia and monitor for adverse effects.
Patient/Family Teaching
- Use exactly as prescribed; do not increase dose.
- Caution regarding drowsiness; avoid driving or operating heavy machinery.
- Warn about potential for dependence.
- Advise against alcohol or other CNS depressants.
Special Considerations
Black Box Warnings:
- Potential for addiction, abuse, and overdose.
- Use with caution, particularly with other CNS depressants.
Genetic Factors: None well established.
Lab Test Interference: None known.
Overdose Management
Signs/Symptoms: Severe sedation, respiratory depression, coma.
Treatment: Supportive care, airway management, gastric lavage if recent ingestion, activated charcoal, and symptomatic treatment. Educate about the risk of overdose especially with concurrent CNS depressants.
Storage and Handling
Storage: Store at room temperature, away from light and moisture.
Stability: Stable under recommended storage conditions.