FDA Adverse Event Reporting System (FAERS): Latest Quartely Data Files

The FDA Adverse Event Reporting System (FAERS) is a database that contains information on adverse event and medication error reports submitted to FDA. The database is designed to support the FDA's post-marketing safety surveillance program for drug and therapeutic biologic products.

美国食品药品监督管理局（FDA）的不良事件报告系统（FAERS）是一个包含提交给FDA的不良事件及药物错误报告信息的数据库。该数据库旨在支持FDA针对药物及治疗性生物制品的市场后安全性监测项目。