Event Group
Event Groups are part of the Adverse Events Module within the Results Section. They provide a way to organize and summarize adverse event data by grouping related events together.
Each Event Group typically represents a category or class of adverse events and includes statistical information such as the number of participants affected and at risk for different event types: deaths, serious events, and other events.
Event Group path is as follows:
Study -> Results Section -> Adverse Events Module -> Event Group
Event Group
Ignite Creation Date:
2025-12-24 @ 11:53 PM
Ignite Modification Date:
2025-12-25 @ 9:49 PM
NCT ID:
NCT00881751
Group ID:
EG001
Title:
Arm II
Description:
Subjects who were enrolled to the sorafenib arm and received at least one dose of study drug.
Sorafenib: oral administration on days 1-28 of a 28 day cycle
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
19
Serious Number At Risk:
43
Other Number Affected:
43
Other Number At Risk:
43
Study:
NCT00881751
Results Section:
NCT00881751
Adverse Events Module:
NCT00881751