Trimethadione

Trimethadione
Clinical data
Trade namesTridione
AHFS/Drugs.comMicromedex Detailed Consumer Information
Pregnancy
category
  • X
Routes of
administration
By mouth
ATC code
Legal status
Legal status
  • In general: ℞ (Prescription only)
Pharmacokinetic data
BioavailabilityHigh
MetabolismDemethylated to dimethadione
Elimination half-life12–24 hours (trimethadione)
6–13 days (dimethadione)
ExcretionRenal
Identifiers
  • 3,5,5-Trimethyl-1,3-oxazolidine-2,4-dione
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.004.406 Edit this at Wikidata
Chemical and physical data
FormulaC6H9NO3
Molar mass143.142 g·mol−1
3D model (JSmol)
  • O=C1N(C(=O)OC1(C)C)C
  • InChI=1S/C6H9NO3/c1-6(2)4(8)7(3)5(9)10-6/h1-3H3 checkY
  • Key:IRYJRGCIQBGHIV-UHFFFAOYSA-N checkY
  (verify)

Trimethadione (Tridione) is an oxazolidinedione anticonvulsant. It is most commonly used to treat epileptic conditions that are resistant to other treatments.

It is primarily effective in treating absence seizures, but can also be used in refractory temporal lobe epilepsy. It is usually administered 3 or 4 times daily, with the total daily dose ranging from 900 mg to 2.4 g. Treatment is most effective when the concentration of its active metabolite, dimethadione, is above 700 μg/mL. Severe adverse reactions are possible, including Steven Johnson syndrome, nephrotoxicity, hepatitis, aplastic anemia, neutropenia, or agranulocytosis. More common adverse effects include drowsiness, hemeralopia, and hiccups.[1][2]

  1. ^ American Medical Association Dept of Drugs (1977). AMA Drug Evaluations (3rd ed.). Littleton, Mass.: Pub. Sciences Group. p. 466. ISBN 978-0-88416-175-2. OCLC 1024170745.
  2. ^ Rodman MJ, Smith DW (1979). Pharmacology and Drug Therapy in Nursing. Lippincott. p. 259. ISBN 978-0-39754-230-7.