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 @ 2:45 AM
Ignite Modification Date:
2025-12-26 @ 1:25 AM
NCT ID:
NCT02809833
Group ID:
EG000
Title:
Tocilizumab for RA in Routine Practice
Description:
Participants from routine clinical practice in Germany who received tocilizumab for RA according to SmPC were observed for up to 12 months. Tocilizumab must have been selected by the treating physician in advance of the study and was not provided by the Sponsor. According to SmPC, tocilizumab was given as 8 mg/kg via IV infusion at 4-week intervals.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
104
Serious Number At Risk:
850
Other Number Affected:
320
Other Number At Risk:
850
Study:
NCT02809833
Results Section:
NCT02809833
Adverse Events Module:
NCT02809833