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 @ 1:16 AM
Ignite Modification Date:
2025-12-25 @ 11:25 PM
NCT ID:
NCT01399593
Group ID:
EG000
Title:
Eculizumab
Description:
Patients were to receive eculizumab 1200 mg prior to allograft transplantation (Day 0, starting approximately one hour prior to kidney allograft reperfusion), eculizumab 900 mg (Days 1, 7, 14, 21, and 28), and eculizumab 1200 mg (Weeks 5, 7 and 9). All doses of eculizumab were administered intravenously.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
43
Serious Number At Risk:
51
Other Number Affected:
51
Other Number At Risk:
51
Study:
NCT01399593
Results Section:
NCT01399593
Adverse Events Module:
NCT01399593