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 @ 10:40 PM
Ignite Modification Date:
2025-12-25 @ 8:11 PM
NCT ID:
NCT00361335
Group ID:
EG000
Title:
IV Period: 2mg/kg Golimumab+ MTX
Description:
Participants who received 2mg/kg IV golimumab and methotrexate (MTX). Follow-up time was counted in this treatment group until the participant started to receive 4mg/kg IV golimumab. Participants may have missed one or more golimumab and/or MTX doses. Participants must have received MTX at some point while receiving 2mg/kg IV golimumab and before receiving 4mg/kg IV golimumab
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
25
Serious Number At Risk:
182
Other Number Affected:
109
Other Number At Risk:
182
Study:
NCT00361335
Results Section:
NCT00361335
Adverse Events Module:
NCT00361335