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 @ 2:53 PM
Ignite Modification Date:
2025-12-25 @ 1:19 PM
NCT ID:
NCT01691859
Group ID:
EG000
Title:
Mepolizumab
Description:
Subjects will receive 100 mg of mepolizumab (in 1ml polypropylene syringe) injected subcutaneously (SC) approximately every 4 weeks.
Deaths Number Affected:
6
Deaths Number At Risk:
None
Serious Number Affected:
79
Serious Number At Risk:
347
Other Number Affected:
314
Other Number At Risk:
347
Study:
NCT01691859
Results Section:
NCT01691859
Adverse Events Module:
NCT01691859