Drug Guide
Methyprylon
Classification
Therapeutic: Sedative and Hypnotic
Pharmacological: Central Nervous System Depressant
FDA Approved Indications
- Short-term management of insomnia
Mechanism of Action
Methyprylon depresses the central nervous system, producing sedative and hypnotic effects, likely through the modulation of GABA-A receptor activity, enhancing GABA's inhibitory effects.
Dosage and Administration
Adult: Initial: 300-600 mg at bedtime. Adjust based on response and tolerance.
Pediatric: Not recommended due to safety concerns.
Geriatric: Lower initial dose recommended, e.g., 300 mg or less, to reduce risk of adverse effects.
Renal Impairment: Adjust dose based on severity; cautious use recommended.
Hepatic Impairment: Use with caution; no specific dosing guidelines available.
Pharmacokinetics
Absorption: Well absorbed orally.
Distribution: Widely distributed, crosses blood-brain barrier.
Metabolism: Metabolized in the liver.
Excretion: Excreted in urine, primarily as metabolites.
Half Life: Approximately 4-8 hours.
Contraindications
- Hypersensitivity to methyprylon or barbiturates.
- Obtain a complete medication history to avoid drug interactions.
Precautions
- Use with caution in elderly, debilitated patients, or those with compromised respiratory function, history of substance abuse, or hepatic impairment.
Adverse Reactions - Common
- Drowsiness, dizziness, headache. (Common.)
- Nausea, vomiting. (Less common.)
Adverse Reactions - Serious
- Respiratory depression, dependence, withdrawal symptoms. (Serious but less common.)
- Anaphylaxis or allergic reactions. (Rare.)
Drug-Drug Interactions
- Other CNS depressants, including alcohol, benzodiazepines, and opioids, which can increase sedation and respiratory depression.
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor for CNS depression, respiratory status, and signs of dependence.
Diagnoses:
- Risk for injury due to dizziness or sedation.
- Risk for dependence.
Implementation: Administer dose as prescribed, monitor patient response, educate on avoiding alcohol and other sedatives.
Evaluation: Assess effectiveness in improving sleep, monitor for adverse effects.
Patient/Family Teaching
- Take medication exactly as prescribed.
- Do not operate machinery or drive until effects are known.
- Avoid alcohol and other CNS depressants.
- Report signs of allergic reactions or excessive sedation.
Special Considerations
Black Box Warnings:
- Respiratory depression, addiction, withdrawal risks associated with barbiturates.
Genetic Factors: N/A
Lab Test Interference: N/A
Overdose Management
Signs/Symptoms: Excessive sedation, respiratory depression, coma, hypotension.
Treatment: Supportive care, airway management, activated charcoal if early, and possibly hemodialysis in severe cases.
Storage and Handling
Storage: Store at room temperature away from moisture, heat, and light.
Stability: Stable under recommended conditions.