Consider the risks and benefits of readministration of Brineura following an anaphylactic reaction. Tell the doctor if they are sick or taking any medication and if they are allergic to any medicines. If you have questions or would like more information about Brineura, contact your child’s doctor. BioMarin Pharmaceutical Inc. Before treatment with Brineura, it is important to discuss your child’s medical history with their doctor. cellulitis or abscess), or and with shunts used to drain extra fluid around the brain. Jean-Jacques Bienaimé - Chairman and … PALYNZIQ ® (pegvaliase-pqpz) Injection; Brineura ® (cerliponase alfa) Vimizim ® (elosulfase alfa) Kuvan ® (sapropterin dihydrochloride) Naglazyme ® (galsulfase) Aldurazyme ® … If anaphylaxis occurs, immediately discontinue infusion and initiate appropriate medical treatment. Serious and severe allergic reactions (anaphylaxis) may occur. We are committed to developing safe and effective therapies and providing those therapies to the broadest group of patients as quickly as possible. BioMarin Pharmaceutical Inc. is a biotechnology company. BioMarin Pharmaceutical Inc… For more information, please see our, Valoctocogene Roxaparvovec for Severe Hemophilia A, PALYNZIQ® (pegvaliase-pqpz) Injection for PKU, Kuvan® (sapropterin dihydrochloride) for PKU, Vimizim® (elosulfase alfa) for Morquio A Syndrome (MPS IVA). As of 2016, BioMarin has six products on the market, each of which is an orphan drug. Brineura® (cerliponase alfa) is indicated to slow the loss of ambulation in symptomatic pediatric patients 3 years of age and older with late infantile neuronal ceroid lipofuscinosis type 2 (CLN2), also known as tripeptidyl peptidase 1 (TPP1) deficiency. Each drug candidate we pursue is guided by a fundamental understanding of the genetics and underlying biology of the condition it will address. Biomarin Pharmaceutical Inc (NASDAQ:BMRN) Q2 2020 Earnings Call Aug 4, 2020, 4:30 p.m. This BioMarin process requires an in person interview at one of our company locations and never requires payment or fees from job applicants. Due to the potential for anaphylaxis, appropriate medical support should be readily available, and patients should be observed closely, during and after Brineura infusion. Talk to your child’s doctor if they have any symptoms that bother them or that do not go away. SAN RAFAEL, Calif., Dec. 21, 2020 /PRNewswire/ -- BioMarin Pharmaceutical Inc. (NASDAQ: BMRN) today announced that children in the open-label long-term extension of the Phase … ... Pharmaceutical Products Wholesale Pharmaceutical Products … You may report side effects to BioMarin Pharmaceutical Inc. at 1-866-906-6100, or the FDA at 1-800-FDA-1088 or go to www.fda.gov/medwatch. PALYNZIQ® (pegvaliase-pqpz) Injection for PKU; Kuvan® (sapropterin dihydrochloride) for PKU; Brineura® (cerliponase alfa) for CLN2 Disease; ALDURAZYME® (laronidase) for MPS I; … Inform patients/caregivers of the signs and symptoms of anaphylaxis and to seek immediate medical care should these occur. We are committed to the communities we treat beyond the therapies we develop. Your child’s doctor should inspect the scalp and collect samples of your child’s cerebrospinal fluid (CSF) prior to each infusion of Brineura, to check that there is no device failure or infections present. Brineura should not be used in patients with active intraventricular access device-related complications (e.g., leakage, device failure, or device-related infection, including meningitis), symptom of acute, unresolved localized infection around the device insertion site (e.g. Your child may receive medication such as antihistamines before Brineura infusions to reduce the risk of reactions. 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