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 @ 4:54 PM
Ignite Modification Date:
2025-12-25 @ 2:36 PM
NCT ID:
NCT03596450
Group ID:
EG000
Title:
Semaglutide
Description:
Participants received semaglutide subcutaneous (s.c.) injection once weekly in addition to up to 2 oral antidiabetic medications as treatment intensification for 2 years. Medication dose and dose escalation was at the discretion of the study physician according to routine practice for medications for glycemic control in participants.
Deaths Number Affected:
9
Deaths Number At Risk:
None
Serious Number Affected:
38
Serious Number At Risk:
634
Other Number Affected:
0
Other Number At Risk:
634
Study:
NCT03596450
Results Section:
NCT03596450
Adverse Events Module:
NCT03596450