Reported Reactions

About Reported Reactions

Reported Reactions is an independent public-data reference site. It counts the adverse event reports that the U.S. Food and Drug Administration has received about human drugs and biologics (20,646,523 reports in FAERS since 2004) and about medical devices (26,136,888 reports in MAUDE) and presents them by drug name, pharmacologic class, device brand, device type, manufacturer, reaction term and month. It is not affiliated with FDA, with any manufacturer, or with any clinical practice.

What it is for

FDA publishes these reports as bulk files and an interface built for programmers. A patient who wants to know what has been reported about a medication or an implant, a pharmacist who wants the reporting history of a product, or a researcher who wants the trend for a reaction term has no simple way to look. This site does the counting and sets each number beside the context needed to read it: the pharmacologic class, the whole database, the trend, and FDA's own statement of what the data cannot show.

What it leaves out

Funding

The site is free to use and funded by advertising that is clearly labelled. Advertisers have no influence over which products appear or how their reports are presented, no advertising is placed inside the caveat block, and the site carries no affiliate links for any health product.

Updates and corrections

The site is rebuilt daily and picks up each openFDA release (FAERS quarterly, MAUDE monthly) as it appears. FDA's record is authoritative. Manufacturers and anyone else who finds a processing error can use the corrections channel; see the methodology for how counts are made.

Contact: contact page.

Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.