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Pharmacy Safe Moderate Evidence
FAERS count additive seriousness classification
by Harvard MIMS Lab (ToolUniverse)
Description
Quantify serious vs non-serious classifications across medicinal products. Only medicinalproducts is required; all other filters (patientsex, patientagegroup, occurcountry) are optional. Use filters sparingly to avoid overly restrictive searches. Data source: FDA Adverse Event Reporting System (FAERS).
Installation
pip install tooluniverseStatus
Published
Reviewer
Automated import
Date Added
2026-03-30
Tags
tooluniverse fda-drug-adverse-event fda adverse-events pharmacovigilance