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:
2025-12-25 @ 1:39 AM
Ignite Modification Date:
2025-12-25 @ 11:55 PM
NCT ID:
NCT01478594
Group ID:
EG001
Title:
Bevacizumab + mFOLFOX6
Description:
Participants received a dose of 5 mg/kg bevacizumab via intravenous infusion every 2 weeks on Days 1 and 15 of each cycle. Participants also received mFOLFOX6 chemotherapy every 2 weeks on Days 1 and 15 of each cycle.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
42
Serious Number At Risk:
87
Other Number Affected:
85
Other Number At Risk:
87
Study:
NCT01478594
Results Section:
NCT01478594
Adverse Events Module:
NCT01478594