医学
肌病
横纹肌溶解症
他汀类
药物与药物的相互作用
内科学
药物相互作用
不利影响
运输机
药品
药理学
生物化学
基因
化学
作者
Wajd Alkabbani,Ryan Pelletier,Michael A. Beazely,Youssef Labib,Breanna Quan,John‐Michael Gamble
出处
期刊:Drug Safety
[Springer Nature]
日期:2022-03-01
卷期号:45 (3): 287-295
被引量:11
标识
DOI:10.1007/s40264-022-01166-3
摘要
IntroductionAn increased risk of myopathy due to a potential interaction between sodium glucose co-transporter-2 inhibitors (SGLT-2i) and HMG-CoA reductase inhibitors (statins) has been suggested by case reports.ObjectiveWe aimed to assess if the reporting of myopathy is disproportionally higher among people using both SGLT-2i and statins compared to using either SGLT-2i or statins alone.MethodsWe conducted a disproportionality analysis using data from the US Food and Drug Administration Adverse Event Reporting System (FAERS). We included reports with at least one antihyperglycemic agent. We compared the proportion of myopathy cases to non-cases between those not using SGLT-2i or statins, using SGLT-2i only, statins only, or both. We calculated the reporting odds ratio and 95% confidence interval. We further stratified by individual SGLT-2i and selected statins (rosuvastatin or atorvastatin).ResultsWe included 688,388 reports with at least one antihyperglycemic agent recorded, of which 9.80% had at least one SGLT-2i agent. Among all included reports, there were a total of 2202 myopathy cases with the majority, 61.26%, occurring among those using statins alone and only 2.72% of myopathy cases were among those using both SGLT-2i and statins together. Reporting of myopathy was not disproportionally higher among those reporting the use of SGLT-2i with statins (reporting odds ratio 2.95, 95% confidence interval 2.27–3.85) compared to statins alone (reporting odds ratio 6.41, 95% confidence interval 5.86–7.02).ConclusionsReports of myopathy were not disproportionally higher among those using SGLT-2i with statins compared to SGLT-2i or statins alone at the class level. Further observational studies may be needed to better assess this interaction at the agent level.
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