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 @ 5:01 PM
Ignite Modification Date:
2025-12-25 @ 2:41 PM
NCT ID:
NCT03207750
Group ID:
EG000
Title:
HRV Porcine Circovirus (PCV)-Free Liquid Group
Description:
Healthy female or male subjects, between and including 6 and 12 weeks (42-90 days) of age at the time of the first study vaccination who received two doses of oral live-attenuated human rotavirus (HRV) vaccine in PCV-free liquid formulation, according to a 0, 2-month schedule, co-administered with one dose of each Pediarix, Hiberix and Prevnar-13 at three timepoints (day 1, month 2 and month 4). PCV-free implies no detection of PCV-1 and PCV-2 according to the limit of detection of the tests used.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
20
Serious Number At Risk:
632
Other Number Affected:
571
Other Number At Risk:
632
Study:
NCT03207750
Results Section:
NCT03207750
Adverse Events Module:
NCT03207750