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 @ 2:17 AM
Ignite Modification Date:
2025-12-26 @ 12:48 AM
NCT ID:
NCT02652260
Group ID:
EG001
Title:
Deferred Switch to MK-1439A (Day 1 to Week 12)
Description:
Participants continued their ongoing ATRIPLA™ regimen orally, once daily for 12 weeks.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
43
Other Number Affected:
25
Other Number At Risk:
43
Study:
NCT02652260
Results Section:
NCT02652260
Adverse Events Module:
NCT02652260