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 @ 11:02 PM
Ignite Modification Date:
2025-12-25 @ 8:32 PM
NCT ID:
NCT04707469
Group ID:
EG001
Title:
Oral Semaglutide 25 mg
Description:
Participants were to take oral semaglutide tablets once daily in a dose escalation manner from week 0 to week 68: 3 mg from week 0 to week 4, 7 mg from week 4 to week 8, 14 mg from week 8 to 12 and 25 mg from week 12 to week 68.
Deaths Number Affected:
6
Deaths Number At Risk:
None
Serious Number Affected:
57
Serious Number At Risk:
534
Other Number Affected:
294
Other Number At Risk:
534
Study:
NCT04707469
Results Section:
NCT04707469
Adverse Events Module:
NCT04707469