FDATracker

FDA Adverse Event Intelligence — Before It Becomes a Regulatory Problem

The FDA receives millions of adverse event reports every year. Buried in that data are the early signals that precede safety label updates, market withdrawals, and litigation. FDATracker surfaces those signals — by drug, by reaction type, by manufacturer — so your pharmacovigilance team sees them before your regulator does.

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Every adverse event report in the FAERS database, organized into searchable, AI-summarized pages. Search by drug name and get a clean summary of the top reactions, severity distribution, and trend direction. No raw data downloads, no SQL queries — just the answer your compliance officer needs in 30 seconds.

Built for pharma compliance teams, biotech analysts, and regulatory consultants who can't afford to miss a safety signal. Starting at $299/month for a single drug class — a fraction of what a missed FAERS signal costs in regulatory response, litigation prep, or label update cycles.

$2499/mo
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