June 30, 2016
Recommended Topic Related To:

Definity

"The U.S. Food and Drug Administration today expanded the approved use of the CoreValve System to treat certain patients who have previously had a tissue aortic valve replacement and are in need of a second one.

This first-of-its-kind use is"...

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Definity

PATIENT INFORMATION

Patients receiving activated DEFINITY® should be instructed to inform their healthcare provider if they:

Last reviewed on RxList: 8/31/2015
This monograph has been modified to include the generic and brand name in many instances.

Report Problems to the Food and Drug Administration

 

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.


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