Acute phenytoin toxicity followed by seizure breakthrough from a ticlopidine-phenytoin interaction

Arch Neurol. 1996 Nov;53(11):1191-2. doi: 10.1001/archneur.1996.00550110143027.

Abstract

Objective: To review a case of a drug-drug interaction between phenytoin sodium and ticlopidine hydrochloride that resulted in acute phenytoin toxicity and permanent memory loss.

Case report: A 63-year-old man who was maintained with a stable dose of phenytoin for treatment of seizures began treatment with ticlopidine following percutaneous transluminal angioplasty and stent placement. Within 3 weeks of beginning treatment with ticlopidine, he experienced acute clinical toxic effects of phenytoin with a maximum measured phenytoin concentration of 162.4 micromol/L. Phenytoin concentration decreased to 36 micromol/L after discontinuing treatment with ticlopidine and reducing the phenytoin dose. Subsequently, the patient developed probable complex partial status epilepticus.

Conclusions: Ticlopidine is a metabolic inhibitor of several drugs. Because of the potential for acute and permanent adverse effects from a drug-drug interaction, phenytoin concentrations should be carefully monitored when beginning or ending ticlopidine therapy.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Drug Interactions*
  • Epilepsy, Complex Partial / drug therapy*
  • Humans
  • Male
  • Middle Aged
  • Phenytoin / adverse effects*
  • Phenytoin / therapeutic use
  • Ticlopidine / adverse effects*
  • Ticlopidine / therapeutic use
  • Time Factors

Substances

  • Phenytoin
  • Ticlopidine