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 @ 2:42 AM
Ignite Modification Date:
2025-12-26 @ 1:20 AM
NCT ID:
NCT00090233
Group ID:
EG000
Title:
RotaTeq™
Description:
Three oral doses (\~6.5x10\^7 to \~1.2x10\^8 IU/dose) of RotaTeq™ (rotavirus vaccine, live, oral, pentavalent) administered at 3 separate visits scheduled 4 to 10 weeks (28 to 70 days) apart.
The Not Completed total includes participants discontinued at any time before the completion of the third study vaccination and/or the 42-day safety follow-up period post vaccination 3.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
863
Serious Number At Risk:
34904
Other Number Affected:
4000
Other Number At Risk:
4800
Study:
NCT00090233
Results Section:
NCT00090233
Adverse Events Module:
NCT00090233