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 @ 1:33 PM
Ignite Modification Date:
2025-12-25 @ 12:33 PM
NCT ID:
NCT02121795
Group ID:
EG001
Title:
FTC/TDF + 3rd Agent (Double-Blind)
Description:
Double-Blind Phase: FTC/TDF 200/300 mg tablet + F/TAF placebo tablet + third agent administered orally once daily for at least 96 weeks.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
31
Serious Number At Risk:
330
Other Number Affected:
226
Other Number At Risk:
330
Study:
NCT02121795
Results Section:
NCT02121795
Adverse Events Module:
NCT02121795