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 @ 12:44 AM
Ignite Modification Date:
2025-12-25 @ 10:57 PM
NCT ID:
NCT01229267
Group ID:
EG000
Title:
V212 [Including High Antigen Lot]
Description:
Participants received V212 Consistency Lot 1, 2, 3 or High Antigen Lot 0.5 mL administered by subcutaneous injection 30 days before and 30, 60, and 90 days after auto-HCT.
Deaths Number Affected:
136
Deaths Number At Risk:
None
Serious Number Affected:
420
Serious Number At Risk:
657
Other Number Affected:
625
Other Number At Risk:
657
Study:
NCT01229267
Results Section:
NCT01229267
Adverse Events Module:
NCT01229267