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 @ 10:35 PM
Ignite Modification Date:
2025-12-25 @ 8:07 PM
NCT ID:
NCT00337935
Group ID:
EG001
Title:
PROCRIT (Epoetin Alfa)
Description:
epoetin alfa administered at 20,000 IU subcutaneously every 2 weeks for a period of 26 weeks
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
39
Serious Number At Risk:
118
Other Number Affected:
99
Other Number At Risk:
118
Study:
NCT00337935
Results Section:
NCT00337935
Adverse Events Module:
NCT00337935