Drug Guide
Zolpidem Tartrate
Classification
Therapeutic: Sedative-Hypnotic for Insomnia
Pharmacological: Imidazopyridine receptor agonist
FDA Approved Indications
- Short-term treatment of insomnia characterized by difficulty with sleep initiation
Mechanism of Action
Zolpidem binds selectively to the alpha-1 subunit of the GABA-A receptor complex, enhancing GABAergic inhibition and leading to sedative effects.
Dosage and Administration
Adult: 5-10 mg at bedtime, with adjustments based on response and tolerability
Pediatric: Not approved for pediatric use
Geriatric: Start with lower doses, typically 5 mg, due to increased sensitivity
Renal Impairment: Use lower dose; monitor closely
Hepatic Impairment: Start with 5 mg; avoid in severe impairment
Pharmacokinetics
Absorption: Rapid absorption, peak plasma levels in about 2 hours
Distribution: Widely distributed, crosses the blood-brain barrier
Metabolism: Primarily hepatic via CYP3A4 enzyme
Excretion: Metabolites excreted in urine
Half Life: 2-3 hours in healthy adults, may be extended in elderly
Contraindications
- Hypersensitivity to zolpidem or any component of the formulation
- History of complex sleep behaviors (e.g., sleepwalking, sleep driving)
Precautions
- Use with caution in patients with a history of substance abuse, hepatic impairment, or respiratory impairment; avoid alcohol and CNS depressants during therapy
Adverse Reactions - Common
- Dizziness (Common)
- Drowsiness (Common)
- Headache (Common)
Adverse Reactions - Serious
- Complex sleep behaviors (e.g., sleepwalking, sleep-driving) (Serious but rare)
- Anaphylaxis or angioedema (Rare)
- Bitter taste, nausea, or allergic reactions (Rare)
Drug-Drug Interactions
- CNS depressants, including alcohol, antidepressants, other sedatives/hypnotics, opioids
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Assess sleep patterns, sleep quality, and adverse effects
Diagnoses:
- Risk for injury due to somnolence or complex sleep behaviors
Implementation: Administer immediately before bedtime; monitor for adverse effects
Evaluation: Evaluate sleep quality, adverse effects, and safety parameters regularly
Patient/Family Teaching
- Take medication exactly as prescribed. Do not increase dose or frequency.
- Avoid alcohol and other CNS depressants.
- Be cautious of activities requiring full alertness (e.g., driving) after waking.
- Report any complex sleep behaviors or unusual reactions.
Special Considerations
Black Box Warnings:
- Complex sleep behaviors (e.g., sleepwalking, sleep eating, sleep driving)
Genetic Factors: None specified
Lab Test Interference: None
Overdose Management
Signs/Symptoms: Excessive sedation, confusion, ataxia, coma
Treatment: Supportive care, airway management, activated charcoal if ingested recently, and specific antagonist (flumazenil) in certain cases under close monitoring
Storage and Handling
Storage: Store at room temperature, away from moisture and light
Stability: Stable under recommended storage conditions for the duration specified by the manufacturer