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 @ 11:07 PM
Ignite Modification Date:
2025-12-25 @ 8:39 PM
NCT ID:
NCT02981069
Group ID:
EG002
Title:
Byetta/Bydureon Plus Dapagliflozin
Description:
Exenatide:
4 weeks of exenatide followed by 12 weeks of Bydureon 2mg sc once weekly PLUS
Dapagliflozin:
16 weeks Dapagliflozin, Farxiga, 10mg
Dapagliflozin: 10mg
Exenatide: Byetta 5 to 10 ug (twice daily) Bydureon 2mg (once weekly)
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
25
Other Number Affected:
7
Other Number At Risk:
25
Study:
NCT02981069
Results Section:
NCT02981069
Adverse Events Module:
NCT02981069