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 @ 9:31 PM
Ignite Modification Date:
2025-12-25 @ 7:16 PM
NCT ID:
NCT03631732
Group ID:
EG002
Title:
B/F/TAF After Week 24
Description:
Participants received B/F/TAF (50/200/25 mg) FDC tablet orally once daily from Week 24 to Week 48, without regard to food. At Week 48, participants who wished to continue on B/F/TAF were given the option to receive B/F/TAF FDC for up to an additional 24 weeks or until they had access to B/F/TAF, whichever occurred first.
Deaths Number Affected:
2
Deaths Number At Risk:
None
Serious Number Affected:
20
Serious Number At Risk:
319
Other Number Affected:
53
Other Number At Risk:
319
Study:
NCT03631732
Results Section:
NCT03631732
Adverse Events Module:
NCT03631732