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 @ 12:03 PM
Ignite Modification Date:
2025-12-25 @ 11:58 AM
NCT ID:
NCT01051661
Group ID:
EG003
Title:
Arepanrix 1D 3Y-10Y Group
Description:
Subjects, male and female, aged 3 years (Y) to 10 years, received 1 dose (D) of the Arepanrix™ vaccine followed by 1 dose of saline placebo at a 21-day interval at a 21-day interval (Days 0 and 21). First doses were administered in the deltoid region of the non-dominant arm (or left arm if dominance is not yet identified). Second doses were administered at a 21-day interval in the deltoid region of the dominant arm (or right arm).
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
37
Serious Number At Risk:
1436
Other Number Affected:
1047
Other Number At Risk:
1436
Study:
NCT01051661
Results Section:
NCT01051661
Adverse Events Module:
NCT01051661