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reporting-adverse-events

Structures adverse-event mentions that OpenMed extracts into FAERS / ICH E2B(R3) reportable fields — suspect drug, reaction (MedDRA PT), seriousness criteria, and outcome. Use when the user needs to build an individual case safety report (ICSR), populate a FAERS submission, map a narrative to E2B(R3) data elements, classify seriousness (death, life-threatening, hospitalization, disability, congenital anomaly), or assign reaction outcomes. Trigger keywords: adverse event, ADR, ICSR, FAERS, E2B, E2B(R3), suspect drug, seriousness, MedDRA, reaction outcome, pharmacovigilance case. Pairs after OpenMed NER: consume Pharmaceutical/Chemical and Disease entities from openmed.analyze_text. MedDRA is licensed and user-supplied — never bundled. De-identify the narrative with openmed.deidentify before any external submission.

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maziyarpanahi/openmed

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