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 @ 5:05 AM
Ignite Modification Date:
2025-12-26 @ 4:09 AM
NCT ID:
NCT01567527
Group ID:
EG000
Title:
Conversion Phase.
Description:
During the Oral Conversion Phase, subjects were cross-titrated from other antipsychotics to oral non-generic aripiprazole monotherapy. Received Oral aripiprazole at a target starting dose of 15 mg/day.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
32
Serious Number At Risk:
459
Other Number Affected:
180
Other Number At Risk:
459
Study:
NCT01567527
Results Section:
NCT01567527
Adverse Events Module:
NCT01567527