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 @ 10:51 PM
Ignite Modification Date:
2025-12-25 @ 8:20 PM
NCT ID:
NCT00543569
Group ID:
EG000
Title:
Tacrolimus/MMF/Basiliximab
Description:
Participants received tacrolimus at a starting dose of 0.20 mg/kg/day, mycophenolate mofetil (MMF) 750 or 1000 mg twice daily (BID), basiliximab administered as a 20 mg bolus injection 2 hours prior to transplantation on Day 0 and a 20 mg bolus injection on Day 3 and tapered corticosteroids for 6 months.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
41
Serious Number At Risk:
79
Other Number Affected:
79
Other Number At Risk:
79
Study:
NCT00543569
Results Section:
NCT00543569
Adverse Events Module:
NCT00543569