April 28, 2017
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ReoPro

"SILVER SPRING, MD ” The US Food and Drug Administration (FDA) is warning of several treatment-related serious adverse events in association with implantable left ventricular assist devices (LVADs) in heart-failure patients.

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ReoPro

Overdosage
Contraindications

OVERDOSE

There has been no experience of overdosage in human clinical trials.

CONTRAINDICATIONS

Because Abciximab may increase the risk of bleeding, Abciximab is contraindicated in the following clinical situations:

Abciximab is also contraindicated in patients with known hypersensitivity to any component of this product or to murine proteins.

This monograph has been modified to include the generic and brand name in many instances.

Last reviewed on RxList: 4/3/2017

Overdosage
Contraindications

Additional ReoPro Information

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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