Associations between Suspected Adverse Drug Reactions of HMG-CoA Reductase Inhibitors and Polypharmacology Using a National Registry Approach

Hasan Yousaf, A. M. Jones
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引用次数: 1

Abstract

Aims: The aim of this study was to explore the suspected adverse drug reaction (ADR) data of five licensed statins in the UK: atorvastatin, fluvastatin, pravastatin, rosuvastatin, and simvastatin. A secondary aim was to determine if there are any associations between the polypharmacological properties of the statins and their associated muscle-related side effects. Methods: The chemical database of bioactive molecules with drug-like properties, European Molecular Biology Laboratory (ChEMBL), was used to obtain data on the pharmacological interactions of statins with human proteins. The Medicines and Healthcare Products Regulatory Agency’s (MHRA) Yellow Card scheme was used to obtain reports of suspected ADRs from 2018 to 2022. The OpenPrescribing database was used to obtain the prescribing rates for statistical interpretation. Results: The study found no significant difference between the statins association with suspected ADRs across all organ classes (X2, p > 0.05). Fluvastatin was found to have a higher incidence of ADRs/100,000 Rx across multiple system organ classes. Conclusions: No significant difference was found between the suspected ADR incidence of the statins across all system organ classes.
采用国家登记方法分析 HMG-CoA 还原酶抑制剂的可疑不良药物反应与多重药理作用之间的关系
目的:本研究旨在探讨英国五种已获许可的他汀类药物(阿托伐他汀、氟伐他汀、普伐他汀、罗苏伐他汀和辛伐他汀)的疑似药物不良反应(ADR)数据。另一个目的是确定他汀类药物的多药理特性与肌肉相关副作用之间是否存在关联。研究方法利用欧洲分子生物学实验室(ChEMBL)具有类药物特性的生物活性分子化学数据库,获取他汀类药物与人类蛋白质的药理相互作用数据。利用药品和保健品监管局(MHRA)的黄卡计划获取了2018年至2022年的疑似药物不良反应报告。使用 OpenPrescribing 数据库获取处方率,以便进行统计解释。结果:研究发现,在所有器官类别中,他汀类药物与疑似不良反应的关联没有明显差异(X2,P > 0.05)。在多个系统器官类别中,氟伐他汀的不良反应发生率较高/100,000 Rx。结论:在所有系统器官类别中,他汀类药物的疑似 ADR 发生率无明显差异。
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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