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基于FDA不良事件报告系统的mepolizumab的现实世界不成比例分析

Huqun Li1, Chongshu Wang2, Aiping Deng1

  • 1Department of Pharmacy, The Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

Frontiers in pharmacology
|December 25, 2023
PubMed
概括

这项研究分析了关于梅波利祖马布不良事件 (AE) 的现实数据. 虽然常见的副作用被注意到,但长期儿科使用中咳和肺炎等意想不到的信号需要进一步调查.

关键词:
喘 喘 是一种这是不成比例的不成比例.长期的长期的长期的这就是Mepolizumab.儿科 儿科 儿科药物监督和药物监督

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Pharmacovigilance01:19

Pharmacovigilance

Post-marketing surveillance is a critical component of pharmaceutical regulation, often uncovering unanticipated adverse drug reactions (ADRs) once a drug is widely used over an extended period.
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...
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