Labeling.cslbehring.ca

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Website: Labeling.cslbehring.ca
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Administer reconstituted Kcentra at a rate of 0.12 mL/kg

CSL Behring FULL PRESCRIBING INFORMATION Kcentra® Prothrombin Complex Concentrate (Human) WARNING: ARTERIAL AND VENOUS THROMBOEMBOLIC COMPLICATIONS

https://labeling.cslbehring.com/PI/US/Kcentra/EN/Kcentra-Prescribing-Information.pdf

Privigen Coding Information - labeling.cslbehring.com

Your single source for Ig solutions Call us now for reimbursement support Privigen reimbursement support is available free of charge through IgIQ, See full prescribing information for complete boxed warning. Privigen

https://labeling.cslbehring.com/PRODUCT-DOCUMENT/US/Privigen/EN/Privigen-Coding-Guide.pdf

Corporate Responsibility - cslbehring.com

At CSL, Corporate Responsibility is about conducting our business ethically and contributing to the economic, social and environmental well-being of our communities.

https://www.cslbehring.com/our-company/corporate-responsibility

IDELVION® 3500 IU Vials Now Available to Provide

KING OF PRUSSIA, Pa. – 23 August 2018 – Global biotherapeutics leader CSL Behring today announced that IDELVION ® [Coagulation Factor IX (Recombinant), Albumin Fusion Protein (rFIX-FP)], its novel, long-acting recombinant albumin fusion protein for treating hemophilia B is now available in a 3500 IU (international unit) vial size. For some patients, the 3500 IU vial size will reduce the

https://www.cslbehring.com/newsroom/2018/20180823-idelvion-3500iu-available-in-us

Clotting Factors - Medical Clinical Policy Bulletins | Aetna

Number: 0131. Policy. Note: REQUIRES PRECERTIFICATION Footnotes for precertifiation required *. Aetna considers anti-hemophilic factor (factor VIII) (e.g., Novoeight, Hemofil M, Koate DVI, Monoclate-P), factor IX (e.g., AlphanineSD, Mononine), and Humate-P or Alphanate medically necessary to prevent or treat hemorrhagic complications in adults and children with hemophilia A, hemophilia B or

http://www.aetna.com/cpb/medical/data/100_199/0131.html

Management of the Bleeding Patient Receiving New Oral

4. Protocols. Our institution has created protocols to help direct the use of factor concentrates in the treatment of life threatening bleeding in patients taking new oral anticoagulants (Figure 1).The initial measures are the same for any bleeding patient, with local intervention and supportive care.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4127295/

FDA Accepts Behring's License Application for Hizentra®

FDA Accepts CSL Behring’s Supplemental Biologics License Application for Hizentra ® Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) Indication . KING OF PRUSSIA, Pa. — 07-19-2017. Global biotherapeutics leader CSL Behring today announced that the U.S. Food and Drug Administration (FDA) has accepted for review the company’s supplemental Biologics License Application (BLA) for

http://kankakee.cslbehring.com/news/csl-behring/FDA-Accepts-Behrings-License-Application-for-Hizentra

Pharmacy Policy Bulletin - PA

Pharmacy Policy Bulletin Title: Hereditary Angioedema Agents Policy #: Rx.01.109 Application of pharmacy policy is determined by benefits and contracts. Benefits may vary based on product line, group, or contract. Some medications may be subject to precertification, age, quantity, or formulary restrictions (ie limits on non-preferred drugs).

https://www.ibx.com/pdfs/providers/pharmacy_information/pharmacy_policies/hereditary_angioedema_agents.pdf

HIGHLIGHTS OF PRESCRIBING INFORMATION

HIGHLIGHTS OF PRESCRIBING INFORMATION These highlights do not include all the information needed to use IDELVION® safely and effectively. See full prescribing information for

https://www.fda.gov/media/96526/download

FDA Approves Hizentra for CIDP Treatment | MDedge Neurology

CSL Behring recently announced that the US Food and Drug Administration (FDA) has approved Hizentra (immune globulin subcutaneous [human] 20% liquid) as the first and only subcutaneous immunoglobulin (SCIg) for the treatment of chronic inflammatory demyelinating polyneuropathy (CIDP) as maintenance therapy to prevent relapse of neuromuscular disability and impairment.

https://www.mdedge.com/neurology/clinical-edge/summary/fda-actions/fda-approves-hizentra-cidp-treatment

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