Ezetimibe-associated rhabdomyolysis: A comprehensive assessment of the USFDA adverse event reporting system using disproportionality analysis, case reviews and meta-analysis of randomized clinical trials.

IF 3.6 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Kannan Sridharan, Gowri Sivaramakrishnan
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引用次数: 0

Abstract

Background: Ezetimibe, a Niemann-Pick C1-like 1 inhibitor, is widely prescribed as a monotherapy or in combination with statins to reduce cholesterol levels. Although generally well-tolerated, concerns have emerged regarding the risk of rhabdomyolysis, particularly with combination therapies. This study aims to evaluate the association between ezetimibe and rhabdomyolysis using data from the United States Food and Drug Administration's Adverse Event Reporting System (USFDA AERS), case reviews, and a meta-analysis of clinical trials.

Methods: We analyzed reports from the USFDA AERS between Q1 2004 and Q2 2024, focusing on cases with rhabdomyolysis with ezetimibe alone or in combination with statins or bempedoic acid. Disproportionality analysis using both frequentist and Bayesian methods was conducted. We also reviewed published case reports and performed a meta-analysis of randomized clinical trials comparing ezetimibe monotherapy with placebo.

Results: Of 29,153,222 reports in AERS, 668 cases met the inclusion criteria. Frequentist and Bayesian analyses indicated an increased risk of rhabdomyolysis with ezetimibe alone and with statin combinations, particularly with simvastatin and atorvastatin. Interaction signal scores suggested statistically significant interactions between ezetimibe and certain statins (atorvastatin and rosuvastatin). Case reviews identified nine published cases, most of which involved ezetimibe in patients on a stable background therapy of statins. The meta-analysis of 3 trials did not show a significant risk for rhabdomyolysis with ezetimibe monotherapy.

Conclusion: This study suggests a potentially possible association between ezetimibe (monotherapy and in combination), and rhabdomyolysis risk. Clinicians should monitor patients closely, particularly those on combination therapies. Further prospective studies are needed to elucidate causality and inform safe prescribing practices.

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来源期刊
CiteScore
7.00
自引率
6.80%
发文量
209
审稿时长
49 days
期刊介绍: Because the scope of clinical lipidology is broad, the topics addressed by the Journal are equally diverse. Typical articles explore lipidology as it is practiced in the treatment setting, recent developments in pharmacological research, reports of treatment and trials, case studies, the impact of lifestyle modification, and similar academic material of interest to the practitioner. Sections of Journal of clinical lipidology will address pioneering studies and the clinicians who conduct them, case studies, ethical standards and conduct, professional guidance such as ATP and NCEP, editorial commentary, letters from readers, National Lipid Association (NLA) news and upcoming event information, as well as abstracts from the NLA annual scientific sessions and the scientific forums held by its chapters, when appropriate.
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