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:
2025-12-25 @ 1:40 AM
Ignite Modification Date:
2025-12-25 @ 11:55 PM
NCT ID:
NCT00419094
Group ID:
EG001
Title:
Keppra XR 2000 mg/Day
Description:
2000 mg/day once daily for 18 weeks (administered as four Keppra XR tablets once daily)
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
12
Serious Number At Risk:
171
Other Number Affected:
87
Other Number At Risk:
171
Study:
NCT00419094
Results Section:
NCT00419094
Adverse Events Module:
NCT00419094