The principal cytochrome P450 isoenzyme associated appears to be CYP2E1, with CYP1A2 and CYP3A4 as more pathways. Around eighty five% of the oral dose seems from the urine in just 24 hours of administration, most since the glucuronide conjugate, with modest amounts of other conjugates and unchanged drug.If concomitant use by using a CYP2D6 inhibito