FDA Adverse Event Reporting System (FAERS) — Drug Safety & Pharmacovigilance Intelligence

The FDA Adverse Event Reporting System (FAERS) is the gold standard

source for post-market drug safety surveillance. This listing delivers

the complete FAERS database — structured, cleaned, and query-ready —

directly in your Snowflake environment.

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Covering 5.6 million adverse event reports from 2018 onwards across

200+ countries, this dataset gives drug safety teams, pharmacovigilance

analysts, regulatory affairs professionals, and medical affairs teams

instant access to the intelligence they need to detect safety signals,

monitor drug reactions, and support regulatory submissions — without

building or maintaining a single data pipeline.

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Every report is cross-linked across 6 structured tables: patient

demographics, suspect drugs, adverse reactions, serious outcomes

(including death, hospitalization, and disability), drug indications,

and therapy dates — all joinable on a single primary key for

multi-dimensional analysis in seconds.

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SCALE & COVERAGE:

- 5.6M+ adverse event reports (2018 Q1 — 2021 Q1)

- 23M+ drug exposure records

- 18M+ adverse reaction records

- 453,000+ death outcome reports

- 1.16M+ hospitalization reports

- 200+ countries represented

- 6 fully structured, cross-linked tables

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WHAT YOU CAN DO IN ONE QUERY:

- Detect emerging drug safety signals by quarter

- Rank drugs by death rate, hospitalization rate, and serious outcome score

- Compare adverse event profiles across drug classes

- Monitor global reporting trends by country and region

- Identify suspect drugs with highest fatality burden

- Support disproportionality analysis and signal detection

- Benchmark your drug's safety profile against the market

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WHO USES THIS DATA:

- Pharmacovigilance teams monitoring post-market drug safety

- Regulatory affairs teams preparing FDA submissions and PSURs

- Medical affairs teams building safety dossiers

- Drug safety officers at pharmaceutical and biotech companies

- CROs conducting safety surveillance for clients

- Health economics and outcomes research (HEOR) teams

- Life sciences consultants and data scientists

- Academic researchers studying drug safety epidemiology

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WHY THIS LISTING:

Most teams accessing FAERS today download raw quarterly ASCII files

from the FDA website, write custom parsers, maintain their own

databases, and spend weeks before running a single query. This listing

eliminates all of that. The data is structured, normalized, and live

in your Snowflake environment the moment you subscribe — query it

alongside your own internal safety data with no ETL, no pipelines,

and no infrastructure to maintain.

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搜集汇总

背景与挑战

背景概述

该数据集提供FDA不良事件报告系统（FAERS）的完整结构化数据，涵盖2018年以来560多万份报告，涉及200多个国家，包含6个相互关联的表，支持药物安全监测、信号检测和多维分析。数据已优化可直接在Snowflake环境中查询，无需额外数据管道维护，适用于药物安全和监管事务等专业团队。