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 @ 4:23 AM
Ignite Modification Date:
2025-12-26 @ 3:26 AM
NCT ID:
NCT05850520
Group ID:
EG003
Title:
All Aflibercept 8 mg
Description:
Pooled aflibercept 8 mg administered every 8 weeks, after 3 or 5 initial injections at 4-week intervals.
Deaths Number Affected:
5
Deaths Number At Risk:
None
Serious Number Affected:
49
Serious Number At Risk:
591
Other Number Affected:
360
Other Number At Risk:
591
Study:
NCT05850520
Results Section:
NCT05850520
Adverse Events Module:
NCT05850520