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:
2025-12-26 @ 10:58 AM
Ignite Modification Date:
2025-12-26 @ 10:58 AM
NCT ID:
NCT03638908
Group ID:
EG000
Title:
Fluoxetine
Description:
Dosing will be
* Week 1-4: 20 mg daily
* Week 5-8: 40 mg daily
* Week 9-12: 60 mg daily
* Week 13-24: 80 mg daily
Fluoxetine
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
8
Other Number Affected:
8
Other Number At Risk:
8
Study:
NCT03638908
Results Section:
NCT03638908
Adverse Events Module:
NCT03638908