Adverse Events Leading to Discontinuation of Study Treatment

Select this option to include the Adverse Events Leading to Discontinuation of Study Treatment listing.

This listing includes the study identifier, planned treatment, USUBJID, body system or organ class affected, the start and end dates for the effect, severity, whether it was serious, the cause of the effect and the outcome.

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