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 @ 4:48 PM
Ignite Modification Date:
2025-12-25 @ 2:33 PM
NCT ID:
NCT02865850
Group ID:
EG001
Title:
Darbepoetin Alfa
Description:
Participants were randomized to Darbepoetin alfa at an initial dose that was based on the current package insert for investigational sites in the United States (US), and the Summary of Product Characteristics (SmPC) for all other investigational sites (non-US) for adult participants with chronic kidney disease on dialysis. For participants already on Darbepoetin alfa, the initial dosing regimen in the study was based on the prior dosing regimen.
Deaths Number Affected:
20
Deaths Number At Risk:
None
Serious Number Affected:
105
Serious Number At Risk:
186
Other Number Affected:
83
Other Number At Risk:
186
Study:
NCT02865850
Results Section:
NCT02865850
Adverse Events Module:
NCT02865850