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 @ 4:08 PM
Ignite Modification Date:
2025-12-25 @ 2:08 PM
NCT ID:
NCT01360866
Group ID:
EG000
Title:
Prior Placebo
Description:
Participants who received placebo with ADT in previous double blind phase 3 studies, received 0.5 to 3 mg/day Brexpiprazole + ADT for weeks 1, 2, 4, 8,14, 20, 26, 32, 38, 44 and 52 with dose adjustment.
Deaths Number Affected:
2
Deaths Number At Risk:
None
Serious Number Affected:
14
Serious Number At Risk:
516
Other Number Affected:
296
Other Number At Risk:
516
Study:
NCT01360866
Results Section:
NCT01360866
Adverse Events Module:
NCT01360866