Ethosuximide
| Clinical data | |
|---|---|
| Trade names | Zarontin, others | 
| AHFS/Drugs.com | Monograph | 
| MedlinePlus | a682327 | 
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| Routes of administration  | By mouth (capsules, solution) | 
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| Pharmacokinetic data | |
| Bioavailability | 93% | 
| Metabolism | liver (CYP3A4, CYP2E1) | 
| Elimination half-life | 53 hours | 
| Excretion | kidney (20%) | 
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| ECHA InfoCard | 100.000.954 | 
| Chemical and physical data | |
| Formula | C7H11NO2 | 
| Molar mass | 141.170 g·mol−1 | 
| 3D model (JSmol) | |
| Chirality | Racemic mixture | 
| Melting point | 64 to 65 °C (147 to 149 °F) | 
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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.