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The principal cytochrome P450 isoenzyme concerned seems to be CYP2E1, with CYP1A2 and CYP3A4 as extra pathways. About 85% of the oral dose appears while in the urine inside 24 hours of administration, most given that the glucuronide conjugate, with tiny quantities of other conjugates and unchanged drug [see OVERDOSAGE] for toxicity data.An incredib