Output Overview Descriptions | Clinical | Adverse Events Report

Adverse Events Report
Running this process generates a pdf, rtf, or html file summary of the adverse events experienced by the subjects in the trial grouped by treatment, gender and race. The inclusion of an additional table showing counts of each adverse event by severity level can be specified.
The PDF and HTML formats also contain hyperlinks in their left pane for ease of navigation to specific reports.
Note: Adverse events must meet or exceed the specified threshold occurrence to be included.
Refer to the Adverse Event Report process description for more information.