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 @ 12:43 PM
Ignite Modification Date:
2025-12-25 @ 12:13 PM
NCT ID:
NCT03824561
Group ID:
EG000
Title:
Vedolizumab 300 mg
Description:
Vedolizumab IV infusion 300 mg, at Weeks 0, 2 and 6, and every 8 weeks thereafter, for up to 54 weeks. Participants received IV infusion as part of routine normal practice.
Deaths Number Affected:
5
Deaths Number At Risk:
None
Serious Number Affected:
82
Serious Number At Risk:
1091
Other Number Affected:
29
Other Number At Risk:
1091
Study:
NCT03824561
Results Section:
NCT03824561
Adverse Events Module:
NCT03824561