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 @ 3:54 PM
Ignite Modification Date:
2025-12-25 @ 1:59 PM
NCT ID:
NCT03329092
Group ID:
EG001
Title:
Meropenem± Colistimethate
Description:
Participants hospitalized with cIAI or NP (including HAP and VAP) were randomized to receive 1000 mg meropenem every 8 hours by IV infusion. A higher dose of 2000 mg was given by IV infusion over 180 minutes if carbapenem resistant pathogen was strongly suspected. Participants were administered colistimethate sodium at investigator's discretion.
Deaths Number Affected:
11
Deaths Number At Risk:
None
Serious Number Affected:
25
Serious Number At Risk:
137
Other Number Affected:
45
Other Number At Risk:
137
Study:
NCT03329092
Results Section:
NCT03329092
Adverse Events Module:
NCT03329092