{"meta":{"dataset":"drug-events","title":"Serious drug adverse event reports by active ingredient (openFDA FAERS)","version":"1.0.0","doi":"10.5281/zenodo.23752994","doiUrl":"https://doi.org/10.5281/zenodo.23752994","conceptDoi":"10.5281/zenodo.23752993","license":"CC BY 4.0","licenseUrl":"https://creativecommons.org/licenses/by/4.0/","attribution":"Source: Probative, Serious drug adverse event reports by active ingredient (openFDA FAERS), version 1.0.0, https://doi.org/10.5281/zenodo.23752994, licensed CC BY 4.0.","citation":"Probative. (2026). Serious drug adverse event reports by active ingredient (openFDA FAERS) (Version 1.0.0) [Data set]. Zenodo. https://doi.org/10.5281/zenodo.23752994","disclaimer":"Not legal advice. This is not medical advice either. A report in the FDA Adverse Event Reporting System is not proof that a drug caused an event; reports come from patients, clinicians and manufacturers, can be duplicated and are not verified. Questions about a medicine are for a health professional, and questions about an injury are for a licensed attorney.","notice":"Probative is a marketing firm, not a law firm; not legal advice.","lastChecked":"2026-10-29","url":"https://probativegrowth.com/data/v1/drug-events/changes.json","humanUrl":"https://probativegrowth.com/data/drug-events/","statusCodes":{"P":"primary source","S":"secondary source","D":"ABA model default","U":"open question"}},"changes":[{"id":"drug-events-2026-10-29-first","date":"2026-10-29","jurisdiction":"US","records":["drug-events:US"],"status":"P","title":"Serious drug adverse event reports by ingredient first published","summary":"FAERS reports received 2024Q3 to 2026Q2 for 312 active ingredients: 2,649,395 drug reports in all, 1,430,033 serious.","source":{"label":"openFDA drug adverse event API","url":"https://open.fda.gov/apis/drug/event/"},"dataset":"drug-events"}]}