Description
Determination of whether or not event was reported to the FDA’s voluntary reporting system, MedWatch.
On-Screen Instructions
Note: MedWatch is the Food and Drug Administration’s (FDA’s) voluntary reporting system for an adverse events associated with the use of a medical product.
Field Type
Radio button (single select)Responses
Yes
No
Guide for Use
No additional information provided.History
Start Date | Spring 2012 |
|---|---|
End Date | n/a |
Change History | n/a |