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 @ 1:49 PM
Ignite Modification Date:
2025-12-25 @ 12:42 PM
NCT ID:
NCT01008995
Group ID:
EG002
Title:
Placebo -> Ustekinumab 45 mg (After CP)
Description:
After controlled period (Week 12-36) - receiving Placebo at Weeks 0 and 4 -\> receiving ustekinumab 45 mg at Week 12 and Week 16
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
2
Serious Number At Risk:
158
Other Number Affected:
27
Other Number At Risk:
158
Study:
NCT01008995
Results Section:
NCT01008995
Adverse Events Module:
NCT01008995