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 @ 11:25 PM
Ignite Modification Date:
2025-12-25 @ 9:10 PM
NCT ID:
NCT02453256
Group ID:
EG002
Title:
Placebo, Then Tocilizumab Open Label
Description:
Participants who received placebo during the double blind period from Baseline to Week 48, received tocilizumab from Week 48 to Week 96.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
7
Serious Number At Risk:
89
Other Number Affected:
46
Other Number At Risk:
89
Study:
NCT02453256
Results Section:
NCT02453256
Adverse Events Module:
NCT02453256