Drug Guide
Ethchlorvynol
Classification
Therapeutic: Sedative, Hypnotic
Pharmacological: GABA-A receptor modulator
FDA Approved Indications
- Short-term management of insomnia
Mechanism of Action
Ethchlorvynol enhances the activity of gamma-aminobutyric acid (GABA) at GABA-A receptors, producing sedative and hypnotic effects.
Dosage and Administration
Adult: Usually 200-300 mg at bedtime, may be adjusted based on response. Not to exceed 600 mg/day.
Pediatric: Not recommended for use in children due to safety concerns.
Geriatric: Use with caution; start at lower doses due to increased sensitivity and risk of adverse effects.
Renal Impairment: Adjust dose based on renal function; close monitoring advised.
Hepatic Impairment: Use with caution; dose adjustment may be necessary.
Pharmacokinetics
Absorption: Well absorbed orally.
Distribution: Widely distributed in body tissues; crosses the blood-brain barrier.
Metabolism: Minimal hepatic metabolism.
Excretion: Primarily excreted unchanged in the urine.
Half Life: Approximately 4-8 hours.
Contraindications
- Hypersensitivity to ethchlorvynol or related compounds.
- Severe hepatic or renal impairment.
Precautions
- Use with caution in elderly patients, patients with a history of substance abuse, or respiratory depression.
- Potential for dependence, abuse, and withdrawal symptoms.
Adverse Reactions - Common
- Drowsiness, dizziness (Common)
- Impaired coordination (Common)
Adverse Reactions - Serious
- Retinal toxicity, visual disturbances (Rare)
- Respiratory depression, neuroleptic malignant syndrome (Rare)
Drug-Drug Interactions
- CNS depressants (e.g., alcohol, benzodiazepines, opioids) increase sedative effects.
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor for signs of excessive sedation, respiratory depression, dependency.
Diagnoses:
- Risk of sedation-related accidents
- Potential for dependence
Implementation: Administer at bedtime, monitor patient response, and assess sleep quality.
Evaluation: Evaluate effectiveness in improving sleep and monitor for adverse effects.
Patient/Family Teaching
- Avoid alcohol and other CNS depressants while taking this medication.
- Do not operate heavy machinery until effects are known.
- Report signs of allergic reactions, unusual sleepiness, or mood changes.
Special Considerations
Black Box Warnings:
- Potential for dependence, abuse, and withdrawal if used long-term or in high doses.
Genetic Factors: No specific genetic testing recommended.
Lab Test Interference: May interfere with sleep studies and liver function tests.
Overdose Management
Signs/Symptoms: Profound sedation, respiratory depression, coma, hypotension.
Treatment: Supportive care, airway management, activated charcoal if ingestion is recent, and benzodiazepines for seizures if necessary.
Storage and Handling
Storage: Store at room temperature away from moisture and light.
Stability: Stable under recommended storage conditions.