Pharmacokinetic interaction of intravenous fentanyl with ketoconazole

Fentanyl is primarily metabolized by CYP3A, but has also been suggested to act as a weak inhibitor of CYP3A. We investigated the influence of CYP3A inhibition by ketoconazole on the pharmacokinetics of intravenously administered fentanyl and the effect of fentanyl on CYP3A activity. A prospective, o...

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Veröffentlicht in:Journal of clinical pharmacology 2015-06, Vol.55 (6), p.708-717
Hauptverfasser: Ziesenitz, Victoria C., König, Sonja K., Mahlke, Nina S., Skopp, Gisela, Haefeli, Walter E., Mikus, Gerd
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Sprache:eng
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