This information is intended for U.S. audiences only.

Intended for U.S. audiences only

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Available Vial Sizes

  • 1 mL dose in a single-use vial (>312 IU)
  • 5 mL dose in a single-use vial (>1560 IU)

Handling and Storage

  • Prior to use, Nabi-HB® [Hepatitis B Immune Globulin (Human)] is stable for up to 39 months when stored unopened between 2 to 8°C (36 to 46°F)1,2
  • Do not freeze
  • Do not use after expiration date
  • Use within 6 hours after the vial has been entered
  • Protect from physical damage

References:

  1. Nabi-HB® Prescribing Information, Biotest Pharmaceuticals Corporation, 2008.
  2. Data on File, ADMA Biologics.

Important Safety Information for Nabi-HB®

Individuals known to have had an anaphylactic or severe systemic reaction to human globulin should not receive Nabi-HB® [Hepatitis B Immune Globulin (Human)] or any other human immune globulin. Individuals who are deficient in IgA have the potential to develop antibodies against IgA and anaphylactic reactions.

In patients who have severe thrombocytopenia or any coagulation disorder that would contraindicate intramuscular injections, Nabi-HB should be given only if the expected benefits outweigh the potential risks.

Nabi-HB is made from human plasma. Products made from human plasma may carry a risk of transmitting infectious agents (e.g., viruses) and, theoretically, the Creutzfeldt-Jakob disease (CJD) agent.

Nabi-HB [Hepatitis B Immune Globulin (Human)], must be administered only intramuscularly for post-exposure prophylaxis.

Vaccination with live virus vaccines (e.g., MMR) should be deferred until approximately three months after administration of Nabi-HB.

The most common adverse reactions associated with Nabi-HB in clinical trials were erythema and ache at the injection site as well as systemic reactions such as headache, myalgia, malaise, nausea and vomiting. No anaphylactic reactions with Nabi-HB have been reported.

Please see the full Prescribing Information for Nabi-HB [Hepatitis B Immune Globulin (Human)].

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.