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 @ 2:10 PM
Ignite Modification Date:
2025-12-25 @ 12:50 PM
NCT ID:
NCT02581995
Group ID:
EG000
Title:
Aflibercept
Description:
Participants were treated according to the EU-PI for treatment of DME for the first year of treatment and received 1 dose of 2 mg aflibercept injected IVT every 4 weeks for 5 consecutive doses, followed by dosing every 8 weeks thereafter until the end of the 52 week treatment period.
Deaths Number Affected:
5
Deaths Number At Risk:
None
Serious Number Affected:
66
Serious Number At Risk:
560
Other Number Affected:
0
Other Number At Risk:
560
Study:
NCT02581995
Results Section:
NCT02581995
Adverse Events Module:
NCT02581995