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 @ 2:01 PM
Ignite Modification Date:
2025-12-25 @ 12:46 PM
NCT ID:
NCT03562195
Group ID:
EG000
Title:
Mepolizumab 100mg
Description:
Participants received 100mg of Mepolizumab subcutaneously every 4 weeks during the total treatment period of 52 weeks in addition to their baseline Standard of Care (SOC) treatment for asthma. Participants received salbutamol as a rescue medication on need basis.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
18
Serious Number At Risk:
149
Other Number Affected:
134
Other Number At Risk:
149
Study:
NCT03562195
Results Section:
NCT03562195
Adverse Events Module:
NCT03562195