May 28, 2017
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Digitek

"SILVER SPRING, MD ” The US Food and Drug Administration (FDA) issued a MedWatch safety alert today regarding premature battery depletion in some implantable cardioverter defibrillators (ICDs) and cardiac-resynchronization-therapy defibrillators ("...

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Digitek




PATIENT INFORMATION

No information provided. Please refer to the WARNINGS and PRECAUTIONS sections.

Last reviewed on RxList: 2/23/2017
This monograph has been modified to include the generic and brand name in many instances.

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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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