Drug Guide
Phenobarbital Sodium
Classification
Therapeutic: Anticonvulsant, Barbiturate
Pharmacological: GABA_A receptor modulator
FDA Approved Indications
- Treatment of seizures, including partial and generalized seizures
Mechanism of Action
Enhances the activity of GABA at GABA_A receptors, increasing chloride ion influx and hyperpolarization of neurons, thereby reducing neuronal excitability.
Dosage and Administration
Adult: Initial dose varies based on condition; typically 30-120 mg/day in divided doses, titrated to response.
Pediatric: Dosing individualized based on weight and age; typically 1-5 mg/kg/day, divided doses.
Geriatric: Start at lower doses due to increased sensitivity; titrate carefully.
Renal Impairment: Adjust dosage accordingly; monitoring required.
Hepatic Impairment: Use with caution; monitor liver function; dosage adjustments may be necessary.
Pharmacokinetics
Absorption: Well absorbed after oral administration.
Distribution: Widely distributed in body tissues; crosses blood-brain barrier.
Metabolism: Primarily hepatic via hydroxylation and conjugation.
Excretion: Renal excretion of unchanged drug and metabolites.
Half Life: Approximately 53-118 hours, variable depending on individual factors.
Contraindications
- History of hypersensitivity to barbiturates
- Porphyria
Precautions
- Respiratory depression, hepatocellular disease, history of addiction, risk of dependence, withdrawal hazards
Adverse Reactions - Common
- Sedation, drowsiness (Common)
- Dizziness (Common)
- Cognitive impairment (Common)
Adverse Reactions - Serious
- Respiratory depression (Rare)
- Agranulocytosis, aplastic anemia (Rare)
- Severe allergic reactions (anaphylaxis, angioedema) (Rare)
Drug-Drug Interactions
- Other CNS depressants, leading to enhanced sedation or respiratory depression; Phenytoin, carbamazepine (altered metabolism); Warfarin (altered anticoagulant effect)
Drug-Food Interactions
- Alcohol may enhance CNS depressant effects.
Drug-Herb Interactions
N/ANursing Implications
Assessment: Assess seizure control, respiratory status, sedation level, liver function.
Diagnoses:
- Risk for injury related to sedation or dizziness
- Impaired airway clearance
Implementation: Administer as prescribed; monitor vital signs and level of consciousness; educate about dependency.
Evaluation: Monitor seizure frequency and side effects for efficacy and safety.
Patient/Family Teaching
- Do not discontinue abruptly to avoid withdrawal seizures.
- Avoid alcohol and CNS depressants.
- Report signs of hypersensitivity, unusual bleeding, or severe side effects.
Special Considerations
Black Box Warnings:
- Dependence and withdrawal symptoms if discontinued abruptly.
- Potential for respiratory depression.
Genetic Factors: None specifically noted for phenobarbital.
Lab Test Interference: May affect liver function tests and drug levels.
Overdose Management
Signs/Symptoms: Respiratory depression, extreme sedation, coma, hypotension, ataxia.
Treatment: Supportive care, airway management, activated charcoal if recent ingestion, possibly hemodialysis for severe cases.
Storage and Handling
Storage: Store at room temperature, 20-25°C (68-77°F), away from moisture and light.
Stability: Stable when stored properly.