[ ADVERSE-EVENT SAFETY SIGNALS ]
What the post-market record is reporting
A bounded public snapshot across FAERS, MAUDE, CAERS, and veterinary reporting. SPEQ Intelligence adds complete source-level term patterns, cross-source context, signal-management actions, and evidence prompts.
Aggregate FDA adverse-event reporting over a rolling 12-month window. Counts reflect reporting activity and completeness, not confirmed causation or comparative risk.
PUBLIC SNAPSHOT
Rolling adverse-event reporting volume and reported-term patterns across FAERS, MAUDE, CAERS, and veterinary sources.
4,436,757Reported events
4Source systems
FAERS — drug adverse events · 910,106 reports · rolling 12 months
MAUDE — device adverse events · 3,475,527 reports · rolling 12 months
CAERS — food, supplement & cosmetic events · 2,668 reports · rolling 12 months