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Differences in drug responsiveness are common, often leading to challenges in optimizing the dosage regimen for a particular patient. Recent advances provide a rational framework for understanding many interpatient differences in drug disposition and their clinical consequences. This article focuses on the cytochrome P-450 enzymes, a superfamily of microsomal drug-metabolizing enzymes that play an important role in oxidative drug metabolism.
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G. Wilkinson (Wed,) studied this question.
www.synapsesocial.com/papers/6a02ac4267f6ea5cc87554dc — DOI: https://doi.org/10.1056/nejmra032424
G. Wilkinson
New England Journal of Medicine
Vanderbilt University
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