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:
2025-12-25 @ 3:53 AM
Ignite Modification Date:
2025-12-26 @ 2:43 AM
NCT ID:
NCT02243202
Group ID:
EG003
Title:
Canagliflozin 300 mg/Phentermine 15 mg
Description:
Participants received co-administration of canagliflozin 300 mg and phentermine 15 mg orally for 26 weeks.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
1
Serious Number At Risk:
83
Other Number Affected:
42
Other Number At Risk:
83
Study:
NCT02243202
Results Section:
NCT02243202
Adverse Events Module:
NCT02243202