FDA adverse event reports as a graph

Real reports from the FDA Adverse Event Reporting System (FAERS) quarterly extracts (—), de-duplicated the way FDA describes: one report per case, its latest version, with cases FDA lists as deleted removed. Each question runs live against xrayGraphDB.

Read this first: a report shows that a product and a reaction were reported together. It does not show that the product caused the reaction. FAERS has duplicates and under-reporting, and counts here are not rates. This is a technology demonstration, not a clinical tool.