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Field Name fda Segment 1, 2, 3 Edition 1, 2, 3
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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 adverse events associated with the use of a medical product.
Field Type
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Responses
Yes
No
Additional Guidance
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Guide for Use
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History
Start Date |
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2012 | |
End Date | n/a |
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Change History | n/a |
Field Name | fda |