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 @ 11:15 PM
Ignite Modification Date:
2025-12-25 @ 8:52 PM
NCT ID:
NCT02607956
Group ID:
EG000
Title:
B/F/TAF
Description:
Blinded Phase: B/F/TAF (50/200/25 mg) FDC + DTG placebo + F/TAF placebo orally once daily for at least 144 weeks, without regard to food.
Deaths Number Affected:
4
Deaths Number At Risk:
None
Serious Number Affected:
64
Serious Number At Risk:
320
Other Number Affected:
250
Other Number At Risk:
320
Study:
NCT02607956
Results Section:
NCT02607956
Adverse Events Module:
NCT02607956