Serious Adverse Events Related to Study Treatment

Select this option to include the Serious Adverse Events Related to Study Treatment listing.

This listing includes the study identifier, planned treatment, USUBJID, Country/Sex/Age, body system or organ class affected, the start and end dates for the effect, outcome, Treatment Start/End/Duration, and average daily dose.

Note: This listing is included in the RTF/PDF output only. It is not included in the interactive output.