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 @ 3:39 PM
Ignite Modification Date:
2025-12-25 @ 1:50 PM
NCT ID:
NCT01681992
Group ID:
EG001
Title:
Inv_MMR_Med Group
Description:
Subjects received one dose of Inv\_MMR, from a mid-range or medium potency lot (Inv\_MMR\_Med), co-administered with VV and HAV vaccines at Day 0. All US subjects were also co-administered PCV-13 vaccine. Approximately 6 weeks later, at Day 42, subjects were administered a dose from a separate lot of the Inv\_MMR vaccine (Inv\_MMR\_Release), for the second dose. Inv\_MMR and VV vaccines were administered subcutaneously in the triceps region of the left and right arm, respectively. HAV and PCV-13 vaccines were administered intramuscularly in the anterolateral region of the right and left thigh, respectively.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
102
Serious Number At Risk:
1497
Other Number Affected:
1311
Other Number At Risk:
1497
Study:
NCT01681992
Results Section:
NCT01681992
Adverse Events Module:
NCT01681992