Reimbursement

For your convenience, below are the NDC, HCPCS, CPT, and ICD-9-CM reimbursement codes for Humate-P^®. (Note: All codes should be verified between the provider and the payer.)

NDC	HCPCS	ICD-9-CM	CPT Code
00053-7615-05 00053-7615-10 00053-7615-20	J7187 (Injection, von Willebrand factor, per IU)	286.4 von Willebrand disease	90765 90766 C8950 C8951 C8957

Our Reimbursement Resource Center provides additional information on insurance matters, coverage trends, patient assistance, and more.

Or, call CSL Behring's Reimbursement Answerline (1-800-676-4266) for assistance with individual case inquiries on a variety of reimbursement services, including:

claim processing reviews
appeals
insurance investigations into product coverage
prior approvals for therapies authorization

You can also write to:
CSL Behring
1020 First Avenue
P.O. Box 61501
King of Prussia, PA 19406-0901
Patient Assistance Program

Important Safety Information

Humate-P is indicated for treatment and prevention of bleeding in adult patients with hemophilia A (classical hemophilia). Humate-P is also indicated in adult and pediatric patients with von Willebrand disease (VWD) for (1) treatment of spontaneous and trauma-induced bleeding episodes, and (2) prevention of excessive bleeding during and after surgery. This applies to patients with severe VWD, and patients with mild and moderate VWD for whom use of desmopressin is known or suspected to be inadequate. Humate-P is not indicated for the prophylaxis of spontaneous bleeding episodes.

Humate-P is contraindicated in individuals with a history of anaphylactic or severe systemic response to antihemophilic factor or von Willebrand factor preparations.

Monitor for intravascular hemolysis and decreasing hematocrit values in patients with A, B, and AB blood groups who are receiving large or frequent doses. Also monitor VWF:RCo and FVIII levels in VWD patients, especially those undergoing surgery.

Thromboembolic events have been reported in VWD patients receiving coagulation factor replacement. Caution should be exercised and antithrombotic measures considered, particularly in patients with known risk factors for thrombosis.

Humate-P is derived from human plasma. The risk of transmission of infectious agents, including viruses and, theoretically, the Creutzfeldt-Jakob disease (CJD) agent, cannot be completely eliminated.

In patients receiving Humate-P in clinical studies for treatment of VWD, the most commonly reported adverse reactions observed by >5% of subjects are allergic-anaphylactic reactions, including urticaria (hives), chest tightness, rash, pruritus (itching), and edema (swelling). For patients undergoing surgery, the most common adverse reactions are postoperative wound or injection-site bleeding, and epistaxis (nosebleed).

Please see full prescribing information.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088.

The information provided herein is solely for use by physicians and healthcare professionals in the United States. The CSL Behring product listed may not have been approved in other countries and may not be available everywhere.