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 @ 1:20 AM
Ignite Modification Date:
2025-12-25 @ 11:28 PM
NCT ID:
NCT00458393
Group ID:
EG000
Title:
TDF/FTC
Description:
Daily oral emtricitabine/tenofovir disoproxil fumarate
Emtricitabine/tenofovir disoproxil fumarate: Fixed-dose coformulation of 200 mg emtricitabine and 300 mg tenofovir disoproxil fumarate
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
92
Serious Number At Risk:
1226
Other Number Affected:
906
Other Number At Risk:
1226
Study:
NCT00458393
Results Section:
NCT00458393
Adverse Events Module:
NCT00458393