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首页> Expert opinion on drug safety> Pregnancy-related adverse events associated with statins: a real-world pharmacovigilance study of the FDA Adverse Event Reporting System (FAERS).

Pregnancy-related adverse events associated with statins: a real-world pharmacovigilance study of the FDA Adverse Event Reporting System (FAERS).

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第一作者： Tingxi,Wu

第一单位： Department of Pharmacy, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.

作者： Tingxi,Wu ^[1] ; Yanfeng,Shi ^[2] ; Bin,Zhu ^[1] ; Dandan,Li ^[3] ; Zhe,Li ^[3] ; Zhigang,Zhao ^[1] ; Yang,Zhang ^[3]

作者单位： Department of Pharmacy, Beijing Tiantan Hospital, Capital Medical University, Beijing, China. ^[1] Center of excellence for Omics Research, National Clinical Research Center for Neurological Diseases, Beijing Tiantan Hospital, Capital Medical University, Beijing, China. ^[2] Department of Pharmacy, Beijing Friendship Hospital, Capital Medical University, Beijing, China. ^[3] Beijing Key Laboratory of Molecular Pharmaceutics and New Drug Delivery Systems, State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing, China. ^[4]

关键词 Bayesian analysis FAERS Pregnancy disproportionality analysis evolocumab fenofibrate statins

主题词人类(Humans);婴儿, 新生(Infant, Newborn);女(雌)性(Female);妊娠(Pregnancy);美国(United States);羟甲基戊二酰基CoA还原酶抑制剂(Hydroxymethylglutaryl-CoA Reductase Inhibitors);普伐他丁(Pravastatin);早产(Premature Birth);死产(Stillbirth);贝叶斯定理(Bayes Theorem);非诺贝特(Fenofibrate);洛伐他汀(Lovastatin);药物副反应报告系统(Adverse Drug Reaction Reporting Systems);美国食品和药物管理局(United States Food and Drug Administration)

DOI 10.1080/14740338.2023.2251888

PMID 37612600

发布时间 2024-03-08

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Expert opinion on drug safety

Expert opinion on drug safety

2024年23卷3期

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