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 @ 10:54 PM
Ignite Modification Date:
2025-12-25 @ 8:22 PM
NCT ID:
NCT00810069
Group ID:
EG002
Title:
Early Intervention (Double Blind)
Description:
Duloxetine flexible dose (60 or 120 milligram \[mg\] daily) for 12 weeks.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
8
Serious Number At Risk:
282
Other Number Affected:
110
Other Number At Risk:
282
Study:
NCT00810069
Results Section:
NCT00810069
Adverse Events Module:
NCT00810069