2003
DOI: 10.1185/030079902125001532
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Clinical pharmacokinetics of fenofibrate

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Cited by 6 publications
(2 citation statements)
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“…The drug is excreted unchanged in urines either as fenofibric acid or as its A c c e p t e d M a n u s c r i p t glucuronide conjugate. No hepatic microsomal metabolism is involved, not being fenofibric acid a substrate for CYP3A4 (102).…”
Section: Fibratesmentioning
confidence: 99%
“…The drug is excreted unchanged in urines either as fenofibric acid or as its A c c e p t e d M a n u s c r i p t glucuronide conjugate. No hepatic microsomal metabolism is involved, not being fenofibric acid a substrate for CYP3A4 (102).…”
Section: Fibratesmentioning
confidence: 99%
“…In contrast, fenofibrate does not have any significant effects on the pharmacokinetics of pravastatin (Gustavson et al 2005) or simvastatin (Bergman et al 2004). Furthermore, in vivo data suggest that fenofibric acid does not undergo significant oxidative metabolism by cytochrome P450 and does not inhibit most cytochrome P450 isoforms (Keating and Ormrod 2002; Telford and Elisaf 2003). …”
Section: Fibrate–statin Combination Therapymentioning
confidence: 99%