prabotulinumtoxinA for injection

  

Information on Injecting PrNUCEIVATM

This content has been created for HCPs.

For further information, please contact nuceivainfo@clarionmedical.com

 

Indications and Usage

PrNUCEIVATM  is indicated for the temporary improvement in the appearance of moderate to severe glabellar lines in adult patients < 65 years of age.

Product Monograph

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Reconstituion

PrNUCEIVATM is supplied as a single dose 100 unit vial. Prior to intramuscular injection, reconstitute each vacuum-dried vial of Nuceiva with sterile 0.9% preservative-free sodium chloride.

Download Nuceiva Reconstitution Instructions

 

Physician Brochure

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Serious Warnings and Precautions

DISTANT SPREAD OF TOXIN EFFECT: The effects of NUCEIVA and all botulinum toxin products may spread from the area of injection to produce symptoms consistent with botulinum toxin effects. These symptoms have been reported hours to weeks after injection. Swallowing and breathing difficulties can be life-threatening and there have been reports of death. The risk of symptoms is probably greatest in children treated for spasticity, but symptoms can occur in adults, particularly in those patients who have underlying conditions that would predispose them to these symptoms.