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Description
338,263 structured reports of serious adverse events linked to gastroenterology drugs from the FDA's FAERS database. The dataset covers events from 2020 to 2025, focusing on outcomes like hospitalization, life-threatening conditions, and death. It was created by RubyIntelligence and includes suspect drugs, MedDRA-coded reactions, patient demographics, and outcome codes.
Use Cases
Signal detection for drug safety based on reported adverse reactions.
Temporal trend analysis of adverse events based on the 2020–2025 coverage.
Demographic profiling of patient outcomes based on included patient variables.
Comparative safety analysis of gastroenterology drugs based on suspect drug listings.
Strengths
338,263 records provide a substantial volume for analysis.
Covers a defined 5-year period from 2020 to 2025.
Focuses on serious adverse events, which are clinically significant.
Limitations
Column-level documentation is absent; field semantics must be inferred after download.
Data may reflect geographic or reporting bias inherent to the FAERS system.
Provenance
Source
FDA FAERS (FDA Adverse Event Reporting System).
Collection Method
Structured adverse event reports submitted to the FDA.
Time Range
2020–2025
Freshness
Last updated 2026-06-17 06:24:14; freshness should be verified.
Geography
Reporter country is included per record; global coverage is likely.
License is unknown; terms of use must be verified before application.