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Research tool·drug discovery·fda_drug_adverse_event

FAERS Count Reporter Qualification

Aggregate FDA adverse event (FAERS) reports for a drug by the primary-source reporter qualification (who submitted the report): Physician, Pharmacist, Other health professional, Lawyer, or Consumer or non-health professional. Answers 'what share of adverse-event reports for drug X came from physicians/pharmacists versus consumers/lawyers?' - a report-quality and reliability dimension (clinician-sourced reports are generally considered more reliable). Only medicinalproduct is required; the optio…

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Overview

Aggregate FDA adverse event (FAERS) reports for a drug by the primary-source reporter qualification (who submitted the report): Physician, Pharmacist, Other health professional, Lawyer, or Consumer or non-health professional. Answers 'what share of adverse-event reports for drug X came from physicians/pharmacists versus consumers/lawyers?' - a report-quality and reliability dimension (clinician-sourced reports are generally considered more reliable). 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 Reporter Qualification 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_reporter_qualification
Tool name
FAERS_count_reporter_qualification
Added
2026-07-29 18:13Z
Tags
tooluniverse
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