Sensitivity of ivacaftor to drug-drug interactions with rifampin, a cytochrome P450 3A4 inducer

被引:20
|
作者
Guimbellot, Jennifer S. [1 ,2 ]
Acosta, Edward P. [1 ,3 ]
Rowe, Steven M. [1 ,2 ,4 ,5 ]
机构
[1] Univ Alabama Birmingham, Gregory Fleming James Cyst Fibrosis Res Ctr, Birmingham, AL USA
[2] Univ Alabama Birmingham, Div Pulm & Sleep Med, Dept Pediat, Birmingham, AL USA
[3] Univ Alabama Birmingham, Dept Pharmacol & Toxicol, Birmingham, AL USA
[4] Univ Alabama Birmingham, Dept Med, Birmingham, AL USA
[5] Univ Alabama Birmingham, Dept Cell Dev & Integrat Biol, Birmingham, AL USA
基金
美国国家卫生研究院;
关键词
CFTR; cytochrome P450; drug-drug interaction; ivacaftor; rifampin;
D O I
10.1002/ppul.23971
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
The CFTR potentiator ivacaftor is responsible for significant clinical improvements among a subset of patients with cystic fibrosis. Because it is a substrate of the cytochrome P450 system, specifically CYP3A4/5, ivacaftor is subject to significant drug-drug interactions, including due to commonly used antimicrobials such as rifampin. While the interaction of rifampin and ivacaftor has been examined in vitro, severe adverse events resulting from this interaction have not been reported in the literature. In this report, we describe the termination of steady, long-term improvement in a patient taking ivacaftor, resulting from the use of rifampin and precipitating a significant pulmonary exacerbation.
引用
收藏
页码:E6 / E8
页数:3
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