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 @ 7:19 PM
Ignite Modification Date:
2025-12-25 @ 4:58 PM
NCT ID:
NCT00576303
Group ID:
EG000
Title:
RO0503821 (1x/4 Weeks)
Description:
Eligible participants started RO0503821 (C.E.R.A) intravenously, at a dose of 120, 200 or 360 µg every four weeks. The dose of C.E.R.A was based on the ESA like epoetin alfa or beta dose of \<8000, 8000-16000, or \>16000 IU/week, administered during the SVP of 4 weeks. The SVP was followed by DTP of 16 weeks, EEP of 8 weeks and LTSP of 28 weeks
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
45
Serious Number At Risk:
200
Other Number Affected:
78
Other Number At Risk:
200
Study:
NCT00576303
Results Section:
NCT00576303
Adverse Events Module:
NCT00576303