Venofer
FDA Approves Procysbi for Rare Genetic Condition »
"The U.S. Food and Drug Administration today approved Procysbi (cysteamine bitartrate) for the management of nephropathic cystinosis in children and adults. Procysbi was granted orphan product designation because it is intended to treat a rare dis"...
Read the FDA Approves Procysbi for Rare Genetic Condition article »
Venofer
PATIENT INFORMATION
Prior to Venofer administration:
- Question patients regarding any prior history of reactions to parenteral iron products
- Advise patients of the risks associated with Venofer
- Advise patients to report any symptoms of hypersensitivity that may develop during and following Venofer administration, such as rash, itching, dizziness, light-headedness, swelling, and breathing problems [see WARNINGS AND PRECAUTIONS]
Last reviewed on RxList: 10/10/2012
This monograph has been modified to include the generic and brand name in many instances.
Additional Venofer Information
Venofer - User Reviews
Venofer User Reviews
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