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 @ 3:29 AM
Ignite Modification Date:
2025-12-26 @ 2:10 AM
NCT ID:
NCT04607005
Group ID:
EG000
Title:
Mepolizumab
Description:
Participants received one dose of 100 mg/mL mepolizumab subcutaneous (SC) on top of Standard of Care (SoC) every 4 weeks during the 52-week treatment period.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
84
Other Number Affected:
47
Other Number At Risk:
84
Study:
NCT04607005
Results Section:
NCT04607005
Adverse Events Module:
NCT04607005