Medical & Healthcare

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.

Publisher / source
maziyarpanahi/openmed (found on GitHub top repositories)
Upstream record
maziyarpanahi/openmed
Version
Version 1
Published
Publication review
Approved for publication · recorded passed scan 2026-11-05
Content fingerprint
86cf2a21c1c2649860495566cabf0bef3bb7e5d0ca6a431d575ac5b9d983507c