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. 2005 Jul 25;360(1460):1617–1638. doi: 10.1098/rstb.2005.1693

Table 1.

Pharmacokinetic consequences of CYP2D6 polymorphism.

pharmacokinetic parameter consequences for the PM relative to EM
bioavailability 2–5 fold
systemic exposure
Cmax 2–6 fold
AUC 2–5 fold
half life 2–6 fold
metabolic clearance 0.1–0.5 fold