Reporter Relatedness For Spontaneous Cases

(Doc ID 863696.1)

Last updated on SEPTEMBER 13, 2009

Applies to:

Adverse Event Reporting System - Version: 4.6.1
Information in this document applies to any platform.


The Relatedness Reporter field in the "Event to drug assessment" tab under the Events tab is
disabled for spontaneous cases and enabled only for clinical study cases. Why it is not enabled
for spontaneous cases?


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