Drug-drug interaction between remdesivir and immunosuppressant agents in a kidney transplant recipient.

IF 0.9 4区 医学 Q4 PHARMACOLOGY & PHARMACY International journal of clinical pharmacology and therapeutics Pub Date : 2022-10-01 DOI:10.5414/CP204239
Toshinori Hirai, Akari Mizuta, Takeshi Sasaki, Kouhei Nishikawa, Takahiro Inoue, Takuya Iwamoto
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引用次数: 4

Abstract

A 60-year-old man was treated with a regimen of controlled-release tacrolimus (2 mg once daily), everolimus (0.5 mg twice daily), methylprednisolone (4 mg once daily), and mizoribine (100 mg twice daily) as an anti-rejection regimen following living-donor kidney transplantation. One year after transplantation, the recipient was admitted to Mie University Hospital (day X; admission date) to treat coronavirus disease 2019 pneumonia. The latest trough concentrations of tacrolimus and everolimus before admission (day X-65) were 4.5 ng/mL and 4.4 ng/mL, respectively. Since tacrolimus concentration was 4.2 ng/mL on day X+3, the dose was adjusted to 1.5 mg once daily to reach the target concentration of 3.0 ng/mL due to the introduction of remdesivir. After starting remdesivir on day X+4, the increased trough concentrations of tacrolimus on day X+6 (6.9 ng/mL) and everolimus on day X+7 (9.2 ng/mL) were observed, which resulted in dose reduction of tacrolimus (0.5 mg once daily) and discontinuation of everolimus. After discontinuation of remdesivir on day X+9, dose titration of controlled-release tacrolimus and restart of everolimus (0.5 mg twice daily) were performed from day X+15. The dose of controlled-release tacrolimus was titrated and fixed to 2 mg once daily at discharge (day X+21). There was no toxicity due to immunosuppressive agents during hospitalization. This case report indicated that remdesivir might interact with cytochrome P450 3A4 substrates, such as tacrolimus and everolimus, and elevate their blood concentrations under high inflammatory conditions.

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肾移植受者中瑞德西韦与免疫抑制剂的药物-药物相互作用。
一名60岁男性在活体肾移植后接受控释他克莫司(2 mg每日1次)、依维莫司(0.5 mg每日2次)、甲基强的松龙(4 mg每日1次)和米佐利滨(100 mg每日2次)作为抗排斥治疗方案。移植后1年,受者入住Mie大学医院(第X天;入院日期)治疗冠状病毒病2019肺炎。入院前(X-65天)他克莫司和依维莫司的最新谷浓度分别为4.5 ng/mL和4.4 ng/mL。由于X+3天他克莫司浓度为4.2 ng/mL,由于引入瑞德西韦,剂量调整为1.5 mg,每日1次,达到3.0 ng/mL的目标浓度。在X+4天开始使用瑞德西韦后,观察到X+6天他克莫司谷浓度增加(6.9 ng/mL), X+7天依维莫司谷浓度增加(9.2 ng/mL),导致他克莫司剂量减少(0.5 mg每日1次)和依维莫司停药。在X+9天停用瑞德西韦后,从X+15天开始进行他克莫司控释剂量滴定和依维莫司重新开始(0.5 mg,每日两次)。他克莫司控释剂量滴定并固定为2mg,每日1次(X+21天)。住院期间无免疫抑制剂引起的毒性反应。该病例报告表明,瑞德西韦可能与细胞色素P450 3A4底物(如他克莫司和依维莫司)相互作用,并在高炎症条件下提高其血药浓度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.70
自引率
12.50%
发文量
116
审稿时长
4-8 weeks
期刊介绍: The International Journal of Clinical Pharmacology and Therapeutics appears monthly and publishes manuscripts containing original material with emphasis on the following topics: Clinical trials, Pharmacoepidemiology - Pharmacovigilance, Pharmacodynamics, Drug disposition and Pharmacokinetics, Quality assurance, Pharmacogenetics, Biotechnological drugs such as cytokines and recombinant antibiotics. Case reports on adverse reactions are also of interest.
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