Drug Guide
Primidone
Classification
Therapeutic: Anticonvulsant/Antiepileptic
Pharmacological: Prodrug for phenobarbital and phenylethylmalonamide
FDA Approved Indications
- Epilepsy (partial seizures, generalized tonic-clonic seizures)
Mechanism of Action
Primidone is metabolized into phenobarbital and phenylethylmalonamide, which enhance GABA-mediated neuronal inhibition, stabilizing neuronal membranes and reducing seizure activity.
Dosage and Administration
Adult: Initial dose: 125-250 mg at bedtime; titrate slowly. Maintenance doses vary.
Pediatric: Dosing based on weight and age, typically starting at 50 mg/day divided doses.
Geriatric: Start at lower dose due to increased sensitivity and risk of adverse effects.
Renal Impairment: Use cautiously; dosage adjustments may be necessary.
Hepatic Impairment: Monitor closely; dosage adjustments recommended.
Pharmacokinetics
Absorption: Well absorbed from gastrointestinal tract.
Distribution: Widespread, crosses blood-brain barrier.
Metabolism: Metabolized in the liver into active metabolites (phenobarbital).
Excretion: Primidone and metabolites excreted primarily in urine.
Half Life: Primidone: approximately 3-7 hours; active metabolites longer.
Contraindications
- Hypersensitivity to primidone, barbiturates, or related drugs.
- Porphyria.
Precautions
- Use cautiously in hepatic impairment, pregnancy, lactation, and with other CNS depressants. Monitor blood counts.
Adverse Reactions - Common
- Drowsiness, dizziness (Common)
- Nausea, vomiting (Common)
- Ataxia, nystagmus (Common)
Adverse Reactions - Serious
- Agranulocytosis, aplastic anemia (Serious but rare)
- Severe hypersensitivity reactions (Rare)
- Stevens-Johnson syndrome (Rare)
Drug-Drug Interactions
- Other CNS depressants, warfarin, oral contraceptives, strong CYP450 inducers or inhibitors.
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor seizure control, hepatic function, blood counts, and CNS status.
Diagnoses:
- Risk for falls due to sedation
- Risk for decreased activity tolerance
Implementation: Administer with food to decrease gastric upset, titrate slowly, monitor blood levels if indicated.
Evaluation: Evaluate seizure frequency, adverse effects, and laboratory parameters regularly.
Patient/Family Teaching
- Take medication exactly as prescribed.
- Do not stop suddenly—risk of withdrawal seizures.
- Report signs of allergic reactions or blood dyscrasias.
- Avoid alcohol and other CNS depressants.
Special Considerations
Black Box Warnings:
- Potential for dependence, withdrawal seizures if discontinued abruptly.
Genetic Factors: N/A
Lab Test Interference: May alter liver function tests, blood counts.
Overdose Management
Signs/Symptoms: Respiratory depression, ataxia, altered mental status, coma.
Treatment: Supportive care, airway management, activated charcoal if recent ingestion, hemodialysis in severe cases.
Storage and Handling
Storage: Store at room temperature, away from moisture and light.
Stability: Stable under recommended storage conditions.