FDA Adverse Events Reporting System Drug Indication 2019

The FDA Adverse Event Reporting System (FAERS) contains information on medication errors, quality complaints and drug-related adverse events that were submitted to the FDA (U.S. Food and Drug Administration) in 2019. The Indication dataset contains all "Medical Dictionary for Regulatory Activities" (MedDRA) terms coded for the indications for use (diagnoses) for the reported drugs (0 or more per drug per event).

美国食品药品监督管理局（FDA）的不良事件报告系统（FAERS）收录了2019年提交至FDA的药物错误、质量投诉以及与药物相关的副作用信息。指示数据集包含了针对报告中药物的使用指示（诊断）所编码的所有“监管活动医学词典”（MedDRA）术语，每个药物每起事件可能有0个或多个。