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Research tool·drug discovery·fda_drug_adverse_event

FAERS Count Drug Characterization

Aggregate FDA adverse event (FAERS) reports for a drug by drugcharacterization, i.e. the role the drug played in the report: Suspect (the drug is suspected of causing the event), Concomitant (co-administered but not suspected), or Interacting (involved in a drug-drug interaction). Answers 'in what fraction of adverse-event reports is drug X the SUSPECT drug versus merely a concomitant/co-administered drug?'. Only medicinalproduct is required; the optional serious filter restricts to serious/non…

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Overview

Aggregate FDA adverse event (FAERS) reports for a drug by drugcharacterization, i.e. the role the drug played in the report: Suspect (the drug is suspected of causing the event), Concomitant (co-administered but not suspected), or Interacting (involved in a drug-drug interaction). Answers 'in what fraction of adverse-event reports is drug X the SUSPECT drug versus merely a concomitant/co-administered drug?'. Only medicinalproduct is required; the optional serious filter restricts to serious/non-serious reports. Data source: FDA Adverse Event Reporting System (FAERS).

Schema

JSON Schema the agent (or your API call) must match.

JSON · 20 lines · 456 chars

Examples (1)

Default FAERS Count Drug Characterization call

public-safeinput
JSON · 4 lines · 56 chars
Expected response keys: success

Anonymous-safe example. Rate-limited; no sign-in required.

Identifiers

Catalog ID
tu_FAERS_count_drug_characterization
Tool name
FAERS_count_drug_characterization
Added
2026-07-29 18:13Z
Tags
tooluniverse
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