FDA Adverse Event Reporting System (FAERS)

FDA Adverse Event Reporting System (FAERS) is offered by S&P Global Market Intelligence from the U.S. Food and Drug Administration (FDA). The FAERS database contains records of adverse event reports, medication error reports and product quality complaints resulting in adverse events that were submitted to the FDA.

This dataset provides details for related events including:

- Demographics
- Drugs
- Indications
- Outcomes
- Reactions
- Sources
- Therapies

搜集汇总

背景与挑战

背景概述

FDA不良事件报告系统（FAERS）是由S&P Global Market Intelligence从美国FDA获取的数据集，收录了提交给FDA的不良事件报告、用药错误报告和产品质量投诉记录。该数据集详细涵盖了人口统计、药物、适应症、结果、反应、来源及疗法等相关事件信息。