- Succinimide anticonvulsant
- Partial Antagonist of T-type Calcium channels within thalamic Neurons
- Decreases burst firing of thalamocortical Neurons, stabilizing CNS nerve activity
- Therapeutic level: 40 to 100 mcg/ml
- Adults (and children age >6 years old)
- Start 500 mg orally once daily
- May increase dose by 250 mg/day every 4 to 7 days
- Maximum: 1.5 grams/day
- Children (ages 3 to 6 years old)
- Start 250 mg orally once daily
- May increase dose by 250 mg/day every 4 to 7 days
- Target dose: 20 mg/kg/day
-
Renal Dosing (CrCl <10 ml/min)
- Reduce dose 25%
- Pregnancy Category C
- Considered Safe in Lactation
- Monitor Complete Blood Count (cbc), and periodic Urinalysis and Liver Function Tests
- Hepatic metabolism
- Highly Protein bound
- Half Life increased in liver disease and in children
- Dose dependent effects (decreases overtime with use, and with divided dosing)
- Nausea or Vomiting
- Decreased appetite (with weight loss)
- Sedation
- Serious
- Neutropenia (rare)
- Mild Leukopenia, however, is common
- Increased Generalized Tonic Clonic Seizures
-
Valproic Acid
-
Valproic Acid increases Ethosuximide levels
- Ethosuximide decreases valproic levels
-
Phenytoin
- Ethosuximide increases Phenytoin levels
-
Primidone
- Ethosuximide decreases Primidone levels
- (2022) Presc Lett, Resource #361206, Antiseizure Medications
- Olson (2020) Clinical Pharmacology, Medmaster Miami, p. 56-7
- Hamilton (2020) Tarascon Pocket Pharmacopoeia
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