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 @ 5:23 PM
Ignite Modification Date:
2025-12-25 @ 2:58 PM
NCT ID:
NCT02699450
Group ID:
EG001
Title:
Arm B: 1.5 mg Faricimab
Description:
Participants received 1.5 mg faricimab every fourth week up to Week 20, for a total of 6 administrations, followed by an observational period up to Week 36. If a participant met pre-specified criteria they received a single dose of 0.3 mg ranibizumab and exited the study.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
7
Serious Number At Risk:
55
Other Number Affected:
31
Other Number At Risk:
55
Study:
NCT02699450
Results Section:
NCT02699450
Adverse Events Module:
NCT02699450