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 @ 5:04 AM
Ignite Modification Date:
2025-12-26 @ 4:06 AM
NCT ID:
NCT04978818
Group ID:
EG001
Title:
Vaxelis
Description:
Participants received 0.5 mL doses of Vaxelis® (3.0 µg/mL PRP-OMP + diphtheria, tetanus, pertussis \[acellular, component\], poliomyelitis \[inactivated\], and hepatitis B \[recombinant deoxyribonucleic acid (rDNA)) administered intramuscularly at age 2 months, 4 months and 6 months along with their other routine immunizations according to the U.S. vaccination schedule for children.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
9
Serious Number At Risk:
167
Other Number Affected:
0
Other Number At Risk:
0
Study:
NCT04978818
Results Section:
NCT04978818
Adverse Events Module:
NCT04978818