Sign in to view source links and access this dataset
Description
928,991 structured adverse event reports for oncology drugs from the FDA's FAERS database, covering the years 2020 to 2025. The dataset includes serious adverse events such as hospitalization, life-threatening outcomes, and death. It was created by RubyIntelligence and last updated on June 17, 2026.
Use Cases
Signal detection for serious adverse drug reactions based on MedDRA-coded reported reactions.
Analyzing temporal trends in oncology drug safety based on reports from 2020 to 2025.
Profiling patient demographics associated with adverse outcomes based on patient demographics fields.
Assessing reporter geographic distribution based on reporter country data.
Strengths
928,991 records provide a substantial volume for analysis.
Covers a defined five-year period from 2020 to 2025.
Focuses on serious adverse events, which are critical for safety monitoring.
Includes structured fields such as suspect drugs, patient demographics, and outcome codes.
Limitations
Column-level documentation is absent; field semantics must be inferred after download.
The dataset is limited to oncology drugs and serious events, excluding other therapeutic areas and non-serious events.
Freshness should be verified as the last update was in 2026.
Provenance
Source
FDA FAERS database.
Collection Method
Likely extracted and filtered from the public FAERS quarterly data files.
Time Range
2020–2025
Freshness
Last updated 2026-06-17 06:24:08
Geography
Global, as indicated by reporter country field.
License is unknown; terms of use should be verified before application.