Dolutegravir drug-drug interactions

被引:4
|
作者
Mondleki, E. [1 ]
Maartens, G. [1 ]
机构
[1] Univ Cape Town, Fac Hlth Sci, Dept Med, Div Clin Pharmacol, Cape Town, South Africa
来源
SAMJ SOUTH AFRICAN MEDICAL JOURNAL | 2022年 / 112卷 / 03期
关键词
PHARMACOKINETICS; PREVALENCE;
D O I
10.7196/SAMJ.2021.v112i3.16316
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Y Dolutegravir is neither an inducer nor an inhibitor of metabolising enzymes, and it therefore has a low propensity to act as a perpetrator of drug-drug interactions. Clinically significant decreases in dolutegravir exposure occur when it is co-administered with strong inducers (e.g. rifampicin, efavirenz) of drug metabolising enzymes and drug efflux transporters for which dolutegravir is a substrate - this can be overcome by increasing the dose of dolutegravir from 50 mg once daily to 50 mg twice daily. Dolutegravir significantly increases metformin plasma exposure: one must not exceed metformin 500 mg twice daily with concomitant dolutegravir. Divalent or trivalent cations chelate dolutegravir. Therefore, concomitant administration of dolutegravir with aluminium- and calcium-containing antacids should be avoided. Dolutegravir can be administered with calcium and iron supplements, provided these are taken together with food.
引用
收藏
页码:194 / 195
页数:2
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