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 @ 12:41 PM
Ignite Modification Date:
2025-12-25 @ 12:12 PM
NCT ID:
NCT02759861
Group ID:
EG000
Title:
Harvoni x 8 or 12 Weeks
Description:
patient will receive 8 or 12 weeks depending on clinical data
harvoni: 8 or 12 weeks of harvoni therapy with monthly nursing visit to monitor alcohol and adherence of harvoni therapy
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
15
Other Number Affected:
13
Other Number At Risk:
15
Study:
NCT02759861
Results Section:
NCT02759861
Adverse Events Module:
NCT02759861