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 @ 5:30 PM
Ignite Modification Date:
2025-12-25 @ 3:04 PM
NCT ID:
NCT02064868
Group ID:
EG000
Title:
Serelaxin + Standard of Care
Description:
Serelaxin (30 μg/kg/day) as continuous 48 hour intravenous infusion plus standard of care.
Deaths Number Affected:
63
Deaths Number At Risk:
None
Serious Number Affected:
214
Serious Number At Risk:
1729
Other Number Affected:
637
Other Number At Risk:
1729
Study:
NCT02064868
Results Section:
NCT02064868
Adverse Events Module:
NCT02064868