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Was the event reported to MedWatch?

Was the event reported to MedWatch?

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 adverse events associated with the use of a medical product.

Field Type

Responses

  • Yes

  • No

Guide for Use

History

Start Date

2012

End Date

n/a

Change History

n/a

Field Name

fda