Infection-related adverse events comparison of Bortezomib, Carfilzomib and Ixazomib:A pharmacovigilance study based on FAERS

药物警戒 Carfilzomib公司 医学 不良事件报告系统 伊扎莫布 硼替佐米 不利影响 多发性骨髓瘤 药理学 肿瘤科 重症监护医学 内科学
作者
Tao Wang,Chenhuan Xiang,Rongrong Guo,Juanjuan Ti,Shaoli Zhang
出处
期刊:Expert Opinion on Drug Safety [Taylor & Francis]
标识
DOI:10.1080/14740338.2025.2494692
摘要

Bortezomib, carfilzomib and ixazomib are the most common proteasomeinhibitors (PIs) used to treat Multiple Myeloma (MM). We conducted a pharmacovigilanceanalysis using the Food and Drug Administration Adverse Event Reporting System(FAERS), aiming to offer a reference for safe and reasonable clinical use. Adverse drug reaction (ADR) signals of bortezomib, carfilzomiband ixazomib were analyzed by statistical methods including Reporting OddsRatio (ROR), Proportional Reporting Ratios (PRR), and Multi-item Gamma-PoissonShrinker (MGPS). A total of 13,977, 8263 and13296 ADRs of bortezomib, carfilzomib andixazomib were analyzed respectively from the FAERS database. The most frequent adverse reactionsignal for bortezomib was peripheral neuropathy; for carfilzomib, it was acutekidney injury; for ixazomib, it was vomiting. Then a total of 43, 23 and 10 infection-related adverseevents of bortezomib, carfilzomib and ixazomib were analyzed. The most commoninfection-related adverse event for bortezomib was cytomegalovirus infection;for carfilzomib, it was bacteremia; and for ixazomib, it was conjunctivitis. In real-world pharmacovigilance studies, PIs are associated withinfection-related adverse events, which is crucial for the safe use of PIs inthe treatment of MM. However, further research is needed to validate thehypotheses generated in this study.
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