Ethosuximide

Ethosuximide
Clinical data
Trade namesZarontin, others
AHFS/Drugs.comMonograph
MedlinePlusa682327
License data
Pregnancy
category
  • AU: D
Routes of
administration
By mouth (capsules, solution)
ATC code
Legal status
Legal status
  • BR: Class C1 (Other controlled substances)
  • US: ℞-only
  • EU: Rx-only
  • In general: ℞ (Prescription only)
Pharmacokinetic data
Bioavailability93%
Metabolismliver (CYP3A4, CYP2E1)
Elimination half-life53 hours
Excretionkidney (20%)
Identifiers
  • (RS)-3-Ethyl-3-methyl-pyrrolidine-2,5-dione
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.000.954
Chemical and physical data
FormulaC7H11NO2
Molar mass141.170 g·mol−1
3D model (JSmol)
ChiralityRacemic mixture
Melting point64 to 65 °C (147 to 149 °F)
  • O=C1NC(=O)CC1(C)CC
  • InChI=1S/C7H11NO2/c1-3-7(2)4-5(9)8-6(7)10/h3-4H2,1-2H3,(H,8,9,10) Y
  • Key:HAPOVYFOVVWLRS-UHFFFAOYSA-N Y
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Ethosuximide, sold under the brand name Zarontin among others, is a medication used to treat absence seizures. It may be used by itself or with other antiseizure medications such as valproic acid. Ethosuximide is taken by mouth.

Ethosuximide is usually well tolerated. Common side effects include loss of appetite, abdominal pain, diarrhea, and feeling tired. Serious side effects include suicidal thoughts, low blood cell levels, and lupus erythematosus. It is unclear if it has adverse effects on the fetus during pregnancy. Ethosuximide is in the succinimide family of medications. Its mechanism of action is thought to be due to antagonism of the postsynaptic T-type voltage-gated calcium channel.

Ethosuximide was approved for medical use in the United States in 1960. It is on the World Health Organization's List of Essential Medicines. Ethosuximide is available as a generic medication. As of 2019, its availability was limited in many countries, with concerns about price fixing in the United States.