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 @ 7:02 PM
Ignite Modification Date:
2025-12-25 @ 4:35 PM
NCT ID:
NCT03829657
Group ID:
EG001
Title:
OL Treatment Period: 0169 Ampreloxetine Rollover
Description:
Participants who received ampreloxetine in study 0169, received 10 mg oral ampreloxetine QD for up to 16 weeks.
Deaths Number Affected:
3
Deaths Number At Risk:
None
Serious Number Affected:
8
Serious Number At Risk:
85
Other Number Affected:
48
Other Number At Risk:
85
Study:
NCT03829657
Results Section:
NCT03829657
Adverse Events Module:
NCT03829657