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Derived biotech safety-and-event intelligence API: openFDA adverse events, enforcement recalls and drug labels fused with SEC EDGAR filings, exposed as computed outputs rather than raw records — composite drug risk scores (0-1) with explainable breakdowns, PRR/ROR pharmacovigilance signals with Evans' criteria classification, therapeutic-class benchmarks, monthly adverse-event trend series with anomaly flags, a regulatory ledger, drug-to-company-to-ticker entity resolution, and AI-generated analyst briefs
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