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 @ 12:49 PM
Ignite Modification Date:
2025-12-25 @ 12:15 PM
NCT ID:
NCT03298061
Group ID:
EG000
Title:
Mepolizumab 300 mg
Description:
Participants who participated in clinical study MEA115921, who required additional dose of \>=5 milligrams per day (mg/day) prednisolone for adequate control of their Eosinophilic Granulomatosis with Polyangiitis (EGPA) received 300 milligrams (mg) mepolizumab subcutaneous (SC) injection every 4 weeks.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
38
Serious Number At Risk:
100
Other Number Affected:
97
Other Number At Risk:
100
Study:
NCT03298061
Results Section:
NCT03298061
Adverse Events Module:
NCT03298061