Processes | Clinical | Adverse Event Report

Adverse Event Report
This process generates SAS reports of adverse events counts and percentages by treatment arm, sex, and race.
What do I need?
This process requires AE and either DM or ADSL. Required variables include USUBJID, TRT01A, ARM, AEDECOD, AEBODSYS, AESER, AGE, SEX, and RACE.
Output/Results
Running this process generates a PDF, rtf, or text file summary of the adverse events contained within the SV domain. Refer to the Adverse Events Report output documentation for detailed descriptions and guides to interpreting your results.