Some references to support "suspect drug" as the correct and standard way of reporting SAE/ADR
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Questions & Answers specific to adverse reaction reporting ...
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reporting of Suspected. Unexpected Suspected. Adverse Reactions .... (section A.2), one reaction/event (section B.2), and one "suspect drug" (section B.4). ...
ec.europa.eu/health/files/eudralex/vol-10/guideline.pdf
[DOC]
SAE Reporting Form V4 - SUSAR Reporting Form (Suspected ...
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14. "SUSPECT DRUG(S) "(include generic name). 20. DID REACTION ABATE AFTER STOPPING DRUG? ... Serious Adverse Event (SAE) Reporting Form, Guidance notes: ...
www.bartsandthelondon.nhs.uk/.../saereporting_form_v4_22120... - Similar
[PDF]
Guidance for Industry
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adverse event reporting as a tool for FDA to detect and alert the public to .... patient, identifiable reporter, "suspect drug", serious adverse event) is Day ...
www.fda.gov/downloads/Drugs/.../Guidances/ucm171672.pdf - Similar