Endpoint · researchGETx402-filings.datalayer.workers.dev /v1/fda/adverse-events ?device=insulin+pump&drug=ibuprofen&limit=10
Adverse event reports for a drug or medical device from the FDA's FAERS and MAUDE systems: total report count and the most frequently reported reactions, ranked.
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Adverse event reports for a drug or medical device from the FDA's FAERS and MAUDE systems: total report count and the most frequently reported reactions, ranked. Returns the interpretation caveat with the data — these are voluntary reports, a report does not establish causation, and counts scale with how widely a product is used.Overview
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