FAERS Count Seriousness By Drug Event
Count the number of adverse event reports classified as serious or non-serious. Only medicinalproduct is required; all other filters (patientsex, patientagegroup, occurcountry) are optional. Use filters sparingly to avoid overly restrictive searches. In results, term Serious means: "The adverse event resulted in death, a life threatening condition, hospitalization, disability, congenital anomaly, or other serious condition", term Non-serious means "The adverse event did not result in any of the…
Overview
Count the number of adverse event reports classified as serious or non-serious. Only medicinalproduct is required; all other filters (patientsex, patientagegroup, occurcountry) are optional. Use filters sparingly to avoid overly restrictive searches. In results, term Serious means: "The adverse event resulted in death, a life threatening condition, hospitalization, disability, congenital anomaly, or other serious condition", term Non-serious means "The adverse event did not result in any of the above". Data source: FDA Adverse Event Reporting System (FAERS).
Schema
JSON Schema the agent (or your API call) must match.
Examples (1)
Default FAERS Count Seriousness By Drug Event call
Anonymous-safe example. Rate-limited; no sign-in required.
Identifiers
- Catalog ID
- tu_FAERS_count_seriousness_by_drug_event
- Tool name
- FAERS_count_seriousness_by_drug_event
- Added
- 2026-04-30 22:47Z
- Tags
- tooluniverse