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 @ 4:30 AM
Ignite Modification Date:
2025-12-26 @ 3:33 AM
NCT ID:
NCT03524118
Group ID:
EG002
Title:
MK-1654 75 mg in Pre-term Infants
Description:
Pre-term infants received clesrovimab 75mg via IM injection and were followed for up to 365 days.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
1
Serious Number At Risk:
40
Other Number Affected:
29
Other Number At Risk:
40
Study:
NCT03524118
Results Section:
NCT03524118
Adverse Events Module:
NCT03524118