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The principal cytochrome P450 isoenzyme involved seems to be CYP2E1, with CYP1A2 and CYP3A4 as supplemental pathways. Around 85% of an oral dose appears in the urine within just 24 hours of administration, most as the glucuronide conjugate, with smaller amounts of other conjugates and unchanged drug. The concomitant use https://conradn530kqv6.popup-blog.com/profile

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