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 @ 12:33 AM
Ignite Modification Date:
2025-12-25 @ 10:40 PM
NCT ID:
NCT00050167
Group ID:
EG000
Title:
Weekly Paclitaxel (WP)
Description:
Weekly Paclitaxel for 12 weeks followed by Fluorouracil + Epirubicin + Cyclophosphamide (FEC) every 3 weeks for 4 cycles
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
81
Serious Number At Risk:
301
Other Number Affected:
297
Other Number At Risk:
301
Study:
NCT00050167
Results Section:
NCT00050167
Adverse Events Module:
NCT00050167