The Rise and Fall of Oral Ketoconazole

被引:70
作者
Gupta, Aditya K. [1 ,2 ]
Lyons, Danika C. A. [2 ]
机构
[1] Univ Toronto, Dept Med, Toronto, ON, Canada
[2] Mediprobe Res Inc, London, ON N5X 2P1, Canada
关键词
ketoconazole; azole antifungal; history; hepatotoxic; indication; HEPATIC-INJURY; LIVER-INJURY; ANTIFUNGAL; PHARMACOKINETICS; INVITRO; STEROIDOGENESIS; INHIBITION; CLEARANCE; IMIDAZOLE; EFFICACY;
D O I
10.1177/1203475415574970
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Ketoconazole was the first broad-spectrum oral antifungal agent available to treat systemic and superficial mycoses. Evidence of hepatotoxicity associated with its use emerged within the first few years of its approval. Growing evidence of serious side effects including endocrine dysregulation, several drug interactions, and death led to the review of oral ketoconazole in 2011. Objective: This article chronicles the use of oral ketoconazole from its introduction to its near replacement in medicine. Conclusion: Due to its hepatotoxic side effects, oral ketoconazole was withdrawn from the European and Australian markets in 2013. The United States imposed strict relabeling requirements and restrictions for prescription, with Canada issuing a risk communication echoing these concerns. Today, oral ketoconazole is only indicated for endemic mycoses, where alternatives are not available or feasible. Meanwhile, topical ketoconazole is effective, safe, and widely prescribed for superficial mycoses, particularly as the first-line treatment for tinea versicolor.
引用
收藏
页码:352 / 357
页数:6
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