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Chinese Journal of Clinical Pharmacology and Therapeutics ›› 2009, Vol. 14 ›› Issue (10): 1183-1192.

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Progress and research in the effect of itraconazole on pharmacokinetic drug-drug interactions

MIAO Cai-yun1, CHEN Yi1, CHEN Jiang-fei2   

  1. 1Department of Pharmacy, Ningbo Women and Children' s Hospital, Ningbo 315012, Zhejiang, China;
    2Department of Pharmacy, Ningbo NO. 1 Hospital, Ningbo 315010, Zhejiang, China
  • Received:2009-09-15 Revised:2009-10-09 Published:2020-10-29

Abstract: Itraconazole, as one of the broad-spectrum antifungal drugs, is an inhibitor of CYP3A4 and P-glycoprotein and was widely used in clinic.CYP3A4 and P-glycoprotein with extensive substrate have present at high levels in gastrointestinal tract, the primary site of absorption for orally administrated drugs, and share a significant overlap in substrate specificity, thus resulting in widely pharmacokinetic interaction by itraconazole, part of which has clinical importance.In this article, the effect of itraconazole on pharmacokinetic drug-drug interactions is reviewed and discussed in order to promote its safe usage.

Key words: itraconazole, antifugal drug, pharmacokinetics, drug-drug interaction

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