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揭示lecanemab的安全性概况:使用FDA不良事件报告系统数据对不良事件的全面分析

Wukun Ge1, Yingyan Yan2, Yaoyao Hu1

  • 1Department of Clinical Pharmacy, Ninghai First Hospital, Ninghai, Ningbo, China.

Journal of Alzheimer's disease : JAD
|January 13, 2025
PubMed
概括

对于阿尔茨海默病的Lecanemab治疗显示了影响神经系统的安全性,并导致像微出血这样的成像异常. 警监控对于优化其使用至关重要.

关键词:
阿尔茨海默病的疾病阿尔茨海默病的疾病.公平的人是公平的.不良事件不良事件不良事件不成比例性分析分析莱卡内马布 (lecanemab) 是一个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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