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 @ 9:48 PM
Ignite Modification Date:
2025-12-25 @ 7:27 PM
NCT ID:
NCT03480932
Group ID:
EG002
Title:
SOF+DAC, Standard
Description:
Sofosbuvir (400mg/daily) + Daclatasvir (60mg/daily) for 12 weeks with standard of care dispensation (4 monthly doses)
Sofosbuvir: Direct acting antiviral agent used for the treatment of hepatitis C
Daclatasvir: Direct acting antiviral agent used for the treatment of hepatitis C
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
50
Other Number Affected:
0
Other Number At Risk:
50
Study:
NCT03480932
Results Section:
NCT03480932
Adverse Events Module:
NCT03480932