The principal cytochrome P450 isoenzyme involved appears to generally be CYP2E1, with CYP1A2 and CYP3A4 as extra pathways. Around 85% of an oral dose appears from the urine within just 24 hrs of administration, most since the glucuronide conjugate, with compact quantities of other conjugates and unchanged drug.If concomitant use by using a CYP2D6 i