BioMarin RareConnections™: Uncommon support for rare disease
BioMarin RareConnections™ is here to help
BioMarin RareConnections: Uncommon support for Morquio A syndrome (MPS IVA)
Rare diseases like Morquio A can bring uncommon challenges. BioMarin RareConnections is here to help you meet these challenges with the resources and assistance you need to gain access to VIMIZIM® (elosulfase alfa). When you enroll with BioMarin RareConnections, you will be connected with a Case Manager who can provide a wide array of personalized support services.
Our dedicated and experienced Case Managers will provide guidance on how you can gain access to VIMIZIM by:
- Helping you understand your insurance coverage and financial assistance options
- Providing you with ongoing product support
- Working with you and your care team to coordinate delivery and administration of your VIMIZIM
To enroll, visit BioMarinRareConnections.com.
Contact the BioMarin RareConnections team for more information by emailing email@example.com
or by calling 1-866-906-6100.
VIMIZIM® (elosulfase alfa) is indicated for patients with mucopolysaccharidosis type IVA (MPS IVA; Morquio A syndrome).
IMPORTANT SAFETY INFORMATION
VIMIZIM is a prescription medicine. Before treatment with VIMIZIM, it is important to discuss your medical history with your doctor. Tell your doctor if you are sick or taking any medication and if you are allergic to any medicines. Also tell your doctor if you are pregnant, planning to become pregnant, or are a nursing mother. Your doctor will decide if VIMIZIM is right for you. If you have questions or would like more information about VIMIZIM, contact your doctor.
Anaphylaxis can occur during any VIMIZIM infusion, as early as 30 minutes from the start and up to 3 hours after infusion, and as late into treatment as the 47th infusion. Hypersensitivity reactions have been observed as early as 30 minutes from the start of infusion but as late as 6 days after infusion.
Serious and severe reactions can happen with VIMIZIM treatment, including life-threatening allergic reactions (anaphylaxis), hives, swelling, cough, shortness of breath, and flushing. You should receive medication such as antihistamines before VIMIZIM infusions to reduce the risk of reactions. If a reaction occurs, the infusion should be slowed or stopped and you may be given additional medication. If a severe reaction occurs, the infusion should be stopped immediately and you will receive appropriate medical treatment.
If you have acute febrile or respiratory illness at the time of VIMIZIM infusion, you may be at higher risk of life-threatening complications from hypersensitivity reactions. If you use supplemental oxygen or continuous positive airway pressure (CPAP), you should have it available during your infusion in the event of a sudden reaction, or extreme drowsiness/sleep from antihistamines.
Spinal cord damage may occur due to the natural MPS IVA disease process. Signs of spinal cord injury include back pain, numbness and paralysis, and loss of bladder and bowel control. Contact your doctor immediately if you develop any of these symptoms.
The most common side effects reported during VIMIZIM infusions included fever, vomiting, headache, nausea, abdominal pain, chills, and fatigue. These are not all the possible side effects with VIMIZIM. Talk to your doctor if you have any symptoms that bother you or that do not go away.
Call your doctor for medical advice about side effects. You may report side effects to BioMarin at 1-866-906-6100 and the FDA by visiting www.fda.gov/medwatch or calling 1-800-FDA-1088.
For more information, call BioMarin RareConnectionsTM at 1-866-906-6100.
Please see accompanying full Prescribing Information, including important warning.