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 @ 3:48 AM
Ignite Modification Date:
2025-12-26 @ 2:36 AM
NCT ID:
NCT01495702
Group ID:
EG001
Title:
NNRTI+FTC/TDF (Randomized Phase)
Description:
Adverse events for this reporting group include those occurring in participants receiving NNRTI+FTC/TDF in the randomized phase.
Participants stayed on their baseline treatment regimen consisting of an NNRTI (EFV, NVP, or RPV) plus FTC/TDF (200/300 mg) (administered according to prescribing information) for up to 96 weeks in the randomized phase, and may have switched to Stribild in the extension phase.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
7
Serious Number At Risk:
143
Other Number Affected:
66
Other Number At Risk:
143
Study:
NCT01495702
Results Section:
NCT01495702
Adverse Events Module:
NCT01495702