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 @ 3:02 AM
Ignite Modification Date:
2025-12-26 @ 1:42 AM
NCT ID:
NCT00087633
Group ID:
EG000
Title:
Prophylaxis Arm
Description:
Pegylated interferon alfa-2a subcutaneously (SC) 135 μg/week for 4 weeks, then increased to 180 μg/week for the next 44 weeks, plus Ribavirin orally 400 mg/day (initial) to 1000 mg/day for patients \<75 kg or 1200 mg/day for patients ≥75 kg PO (escalated) (maximum) administered orally
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
25
Serious Number At Risk:
54
Other Number Affected:
54
Other Number At Risk:
54
Study:
NCT00087633
Results Section:
NCT00087633
Adverse Events Module:
NCT00087633