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 @ 12:53 AM
Ignite Modification Date:
2025-12-25 @ 11:08 PM
NCT ID:
NCT02287467
Group ID:
EG000
Title:
Arm A: hIVIG
Description:
Participants will receive a single infusion of intravenous hyperimmune immunoglobulin (IVIG), administered over approximately 2 hours on Day 0. Participants will also receive SOC treatment for the flu.
Intravenous hyperimmune immunoglobulin (IVIG): Administered intravenously (IV) at a dose of 0.25 g/kg (up to a maximum of 24.75 g, corresponding to approximately 100 kg actual body weight)
Deaths Number Affected:
6
Deaths Number At Risk:
None
Serious Number Affected:
25
Serious Number At Risk:
156
Other Number Affected:
13
Other Number At Risk:
156
Study:
NCT02287467
Results Section:
NCT02287467
Adverse Events Module:
NCT02287467