Predicting drug kinetics and dynamics in an individual patient is a worthy goal and has some chance of success for drugs subject to marked pharmacogenetic differences. Howeer, one should not expect any prediction success for drugs primarily metabolized by the major cytochrome P450 enzyme, CYP3A4, whether one uses an exogenous drug or an endogenous metabolic process, such as the oxidation of cortisol. Clinical Pharmacology & Therapeutics (2009); 86, 2, 133–134 doi:10.1038/clpt.2009.102
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Leslie Z. Benet (2009) studied this question.
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