Report Adverse Events

Preferred Label : Report Adverse Events;

NCIt definition : The healthcare provider or setting must report adverse events of interest to the Manufacturer, MedWatch, and/or a REMS Program.;

NCI Metathesaurus CUI : CL509312;

Details

Origin ID

C128520;

UMLS CUI

C4288300;

Automatic exact mappings (from CISMeF team)
- Reporter of adverse event [LOINC component]
- reports of adverse events [Blood Transfusion thesaurus concept]
Semantic type(s)
- Health Care Activity [UMLS semantic type]
concept_is_in_subset
- FDA Structured Product Labeling Terminology [NCIt concept]
- SPL REMS Requirement Terminology [NCIt concept]

Keyword's position in hierarchy(ies) :

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