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 @ 10:55 PM
Ignite Modification Date:
2025-12-25 @ 8:23 PM
NCT ID:
NCT02831569
Group ID:
EG000
Title:
Loxoprofen Sodium/Methocarbamol [FDC]
Description:
The subjects were administered 2 Loxoprofen sodium/methocarbamol combination \[Fixed Dose Combination (FDC)\] film-coated tablets orally 3 times daily after each meal for 2 weeks.
Each 2 tablets contained Loxoprofen sodium hydrate 68.1 mg and methocarbamol 500 mg.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
80
Other Number Affected:
0
Other Number At Risk:
80
Study:
NCT02831569
Results Section:
NCT02831569
Adverse Events Module:
NCT02831569