FDA不良反应

FDA不良反应数据库收集了上报FDA不良反应报告系统的数据，这些数据来源于发生在全球用药相关的自发性安全报告，该库收集了FDA在2004年至2023年期间公布的不良反应报告数据，目前有1.9KW+份报告数据，病例报告中包含患者用药药物信息、不良反应信息、患者治疗(疾病转归)信息、报告来源等信息。通过该库可以让用户了解上市药品存在的不良反应，及时有效控制用药风险，保障患者用药安全。

The FDA Adverse Event Database collects data submitted to the FDA Adverse Event Reporting System. These data originate from spontaneous drug-related safety reports across the globe. The database gathers adverse event report data released by the FDA between 2004 and 2023, and currently holds over 19 million report records. Each case report contains information such as the patient's medication details, adverse event records, patient treatment and disease outcome data, as well as report source information. This database enables users to gain insights into adverse events associated with marketed drugs, effectively control medication risks in a timely manner, and ensure patient medication safety.

搜集汇总

背景与挑战

背景概述

FDA不良反应数据集包含2004-2023年全球上报的1.9KW+份药品不良反应报告，涵盖用药信息、不良反应表现和治疗转归等详细信息，用于监测药品安全性和控制用药风险。