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 @ 9:28 PM
Ignite Modification Date:
2025-12-25 @ 7:14 PM
NCT ID:
NCT03713632
Group ID:
EG003
Title:
Any AIN457 Q2W
Description:
Subjects who received at least 1 dose of secukinumab 300 mg Q2W dose (including subjects who switched from placebo to secukinumab Q2W at Week 16). Adverse events were assessed up to Week 60
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
22
Serious Number At Risk:
261
Other Number Affected:
174
Other Number At Risk:
261
Study:
NCT03713632
Results Section:
NCT03713632
Adverse Events Module:
NCT03713632