Exploration of adverse events associated with risdiplam use: Retrospective cases from the US Food and Drug Administration Adverse Event Reporting System (FAERS) database

作者全名:"Yu, Lurong; Liu, Limei"

作者地址:"[Yu, Lurong] Chongqing Med Univ, Coll Tradit Chinese Med, Chongqing, Peoples R China; [Liu, Limei] Chongqing YouYou BaoBei Womens & Childrens Hosp, Pharm Dept, Chongqing, Peoples R China"

通信作者:"Liu, LM (通讯作者),Chongqing YouYou BaoBei Womens & Childrens Hosp, Pharm Dept, Chongqing, Peoples R China."

来源:PLOS ONE

ESI学科分类:Multidisciplinary

WOS号:WOS:001181701600029

JCR分区:Q1

影响因子:2.9

年份:2024

卷号:19

期号:3

开始页: 

结束页: 

文献类型:Article

关键词: 

摘要:"Risdiplam is a new drug for treating spinal muscular atrophy (SMA). However, pharmacovigilance analyses are necessary to objectively evaluate its safety-a crucial step in preventing severe adverse events (AEs). Accordingly, the primary objective of the current study was to examine the AEs associated with risdiplam use based on real-world data obtained from the US Food and Drug Administration Adverse Event Reporting System (FAERS) database. More specifically, we examined incidents reported between the third quarter of 2020 and the second quarter of 2023. The imbalance of risdiplam-related AEs was evaluated by computing the reporting odds ratio. A total of 5,406,334 reports were thoroughly reviewed. By removing duplicate reports, we identified 1588 reports in which risdiplam was the main suspected drug whose use was accompanied by 3470 associated AEs. Among the included AEs, 703 were categorized as serious and 885 as non-serious. Risdiplam use induced AEs across 18 organ systems, resulting in 130 positive signals. Notably, we detected new AE signals, including cardiac arrest, nephrolithiasis, tachycardia, loss of libido, and elevated hepatic enzyme activities; however, no ophthalmologic toxicity was reported. Although these new adverse reaction signals associated with risdiplam have been defined, long-term clinical studies are needed to confirm these findings. Nevertheless, our findings provide a valuable reference for improving the clinical management of SMA."

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