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 @ 4:58 AM
Ignite Modification Date:
2025-12-26 @ 3:58 AM
NCT ID:
NCT01435018
Group ID:
EG002
Title:
Paclitaxel (PTX) Plus Co-formulated EFV/FTC/TDF
Description:
Paclitaxel plus ART (co-formulated Efavirenz/Emtricitabine/Tenofovir Disoproxil Fumarate)
Deaths Number Affected:
55
Deaths Number At Risk:
None
Serious Number Affected:
55
Serious Number At Risk:
138
Other Number Affected:
133
Other Number At Risk:
138
Study:
NCT01435018
Results Section:
NCT01435018
Adverse Events Module:
NCT01435018