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 @ 1:37 AM
Ignite Modification Date:
2025-12-25 @ 11:53 PM
NCT ID:
NCT04774094
Group ID:
EG000
Title:
CAZ-AVI
Description:
Participants received CAZ-AVI (Zavicefta), 2.5 g (ceftazidime 2g + avibactam 0.5g), IV as 2 hours infusion every 8 hours for a minimum of 7 days and a maximum of 14 days. Participants were followed up to maximum of 32 days after the last dose of study intervention.
Deaths Number Affected:
17
Deaths Number At Risk:
None
Serious Number Affected:
35
Serious Number At Risk:
235
Other Number Affected:
43
Other Number At Risk:
235
Study:
NCT04774094
Results Section:
NCT04774094
Adverse Events Module:
NCT04774094