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:
2025-12-26 @ 11:07 AM
Ignite Modification Date:
2025-12-26 @ 11:07 AM
NCT ID:
NCT04927312
Group ID:
EG000
Title:
PF-06947386 + Metronidazole
Description:
Participants received intravenous (IV) infusion of PF-06947386 (2.0 gram (g) of ceftazidime and 0.5 g of avibactam) every 8 hours, immediately followed by an IV administration of metronidazole (0.5 g) for 60 minutes. Participants received a minimum of 5 full days (15 doses) of IV study intervention up to a maximum of 14 full days (42 doses) of study intervention.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
3
Serious Number At Risk:
60
Other Number Affected:
34
Other Number At Risk:
60
Study:
NCT04927312
Results Section:
NCT04927312
Adverse Events Module:
NCT04927312