| Literature DB >> 22293514 |
Mark Naccarato1, Deborah Yoong, Colin Kovacs, Kevin Gough.
Abstract
The cytochrome P450 isoforms primarily involved in clobazam metabolism are CYP3A4 and 2C19. Drugs that modulate these enzymes would then be expected to alter the exposure of clobazam and its major metabolites. Etravirine, a second-generation non-nucleoside reverse transcriptase inhibitor has been shown to induce CYP3A4, while inhibiting CYP2C9 and CYP2C19. We report a case in which a potential drug interaction between clobazam and etravirine may have led to increased concentrations of clobazam and its pharmacologically active metabolite, N-desmethylclobazam, causing neurotoxic symptoms.Entities:
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Year: 2011 PMID: 22293514 DOI: 10.3851/IMP1953
Source DB: PubMed Journal: Antivir Ther ISSN: 1359-6535