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 @ 9:20 PM
Ignite Modification Date:
2025-12-25 @ 7:07 PM
NCT ID:
NCT03933904
Group ID:
EG000
Title:
Sirolimus
Description:
For adults, the treatment began with a loading dose of 5 mg/m² on Day 1, designed to quickly achieve therapeutic levels of sirolimus. This loading dose was rounded to the nearest milligram and could be adjusted at the discretion of the prescribing physician based on individual tolerability and clinical judgment.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
1
Serious Number At Risk:
7
Other Number Affected:
7
Other Number At Risk:
7
Study:
NCT03933904
Results Section:
NCT03933904
Adverse Events Module:
NCT03933904