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.

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.

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https://x402-filings.datalayer.workers.dev/v1/fda/adverse-events?device=insulin+pump&drug=ibuprofen&limit=10

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https://x402-filings.datalayer.workers.dev/v1/fda/adverse-events?device=insulin+pump&drug=ibuprofen&limit=10

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cap_01M1A59RGHC17E84NEA62N5SNQ

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