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| (ETH-oh-SUX-ih-mide) |
| Zarontin |
| Class: Anticonvulsant/succinimide |
Action Elevates seizure threshold and suppresses paroxysmal spike and wave activity associated with lapses of consciousness common in absence (petit mal) seizures.
Indications Control of absence (petit mal) seizures.
Contraindications Hypersensitivity to succinimides.
ADULTS & CHILDREN ³ 6 YR: PO 500 mg/day. Optimal dose for most children is 20 mg/kg/day. Maintenance therapy: Individualize dose. Increase daily dose slowly by 250 mg q 4 to 7 days until control is achieved with minimal side effects. Doses exceeding 1.5 g/day should be administered in divided doses under strict medical supervision. CHILDREN 3–6 YR: INITIAL DOSE: PO 250 mg/day.
Hydantoins: May increase serum hydantoin levels. Primidone: Lower primidone and phenobarbital levels may occur.
Lab Test Interferences None well documented.
CNS: Drowsiness; headache; dizziness; euphoria; hiccoughs; irritability; hyperactivity; lethargy; fatigue; ataxia; psychological disturbances such as sleep disorders; night terrors; poor concentration; aggressiveness. DERM: Urticaria; Stevens-Johnson syndrome; systemic lupus erythematosus; pruritic erythematous rash; hirsutism. EENT: Myopia. GI: Anorexia; GI upset; nausea; vomiting; cramps; epigastric and abdominal pain; weight loss; gum hypertrophy; tongue swelling. GU: Vaginal bleeding; microscopic hematuria. HEMA: Leukopenia; agranulocytosis; pancytopenia; bone marrow suppression; eosinophilia.
Pregnancy: Anticonvulsant drugs have been observed to increase the incidence of birth defects. Hematologic effects: Blood dyscrasias, including fatal cases, have occurred. Periodic blood counts should be done. Hepatic or renal impairment: Use caution and perform periodic function tests. Lupus: Cases of systemic lupus erythematosus have occurred. Withdrawal: Do not withdraw drug abruptly as this may precipitate absence (petit mal) status; proceed slowly when increasing or decreasing dose.
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