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 @ 6:29 PM
Ignite Modification Date:
2025-12-25 @ 3:59 PM
NCT ID:
NCT02506868
Group ID:
EG000
Title:
BCD-066
Description:
Patients in this arm received weekly subcutaneous injections of BCD-066 (darbepoetin alfa) with dose level titration to maintain target hemoglobin level (100 - 120 g/l) for 52 weeks
Darbepoetin alfa: Weekly sc administration of darbepoetin alfa
Deaths Number Affected:
5
Deaths Number At Risk:
None
Serious Number Affected:
19
Serious Number At Risk:
98
Other Number Affected:
84
Other Number At Risk:
98
Study:
NCT02506868
Results Section:
NCT02506868
Adverse Events Module:
NCT02506868