Observed arrival · 2026-10-01
Reported Reactions puts FDA adverse-event reports in reach
A searchable guide to adverse-event reports the FDA received for medicines and medical devices, with prominent cautions about what those reports can and cannot establish.
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- People researching reports about a medicine or medical device
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- Drug pages require at least 200 FDA reports and device pages at least 150; the site warns that report counts cannot establish incidence or compare device-event rates.
Field notes
The page sets separate thresholds for creating product pages: 200 reports for a drug name and 150 for a device name. Its latest closed-quarter figures cover April–June 2026, while the stated device-data cutoff extends through August 31, 2026. The site cites FDA and openFDA cautions that reports are not verified measures of causation or event rates.
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Editorial observations of this landing page, not a rating.
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