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 @ 5:42 PM
Ignite Modification Date:
2025-12-25 @ 3:11 PM
NCT ID:
NCT02335268
Group ID:
EG000
Title:
Model Group A
Description:
Starting dose 750 µg of romiplostim once a week (7d ± 2d), subcutaneous injection, 4 months maximum duration for responders treatment period was extended for up to 1 year (8 months extension period). The dose was adjusted based on the subject's platelet count.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
12
Serious Number At Risk:
51
Other Number Affected:
10
Other Number At Risk:
51
Study:
NCT02335268
Results Section:
NCT02335268
Adverse Events Module:
NCT02335268