Ordering Information

HyperHEP B S/D is available through the following distributors:

ASD Specialty Healthcare 1-800-746-6273  

Cardinal Health SPD 1-866-677-4844  

Caribe 1-787-258-3444  

FFF Enterprises 1-800-843-7477  

Henry Schein 1-800-772-4346  

McKesson Medical-Surgical 1-855-571-2100  

McKesson Plasma and Biologics 1-877-625-2566  

Prodigy Health 1-877-693-4376  

Contact Grifols for more information on HyperHEP B S/D.

Customer Service: 1-800-243-4153

Medical Information: 1-800-520-2807

Email: customer.service@grifols.com

HyperHEP B® S/D (hepatitis B immune globulin [human]) is indicated for postexposure prophylaxis in the following situations: acute exposure to blood containing HBsAg, perinatal exposure of infants born to HBsAg-positive mothers, sexual exposure to an HBsAg-positive person, and household exposure to persons with acute HBV infection.

HyperHEP B S/D should be given with caution to patients with a history of prior systemic allergic reactions following the administration of human immunoglobulin preparations. Epinephrine should be available.

In patients who have severe thrombocytopenia or any coagulation disorder that would contraindicate intramuscular injections, hepatitis B immune globulin (human) should be given only if the expected benefits outweigh the risks.

Local pain and tenderness at the injection site, urticaria, and angioedema may occur; anaphylactic reactions, although rare, have been reported following the injection of human immunoglobulin preparations. Administration of live virus vaccines (eg, MMR) should be deferred for approximately 3 months after hepatitis B immune globulin (human) administration.

HyperHEP B S/D is made from human plasma. Products made from human plasma may contain infectious agents, such as viruses, and, theoretically, the Creutzfeldt-Jakob disease (CJD) agent that can cause disease. There is also the possibility that unknown infectious agents may be present in such products.

Please see full Prescribing Information for HyperHEP B S/D.

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.