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All plasma units used in the manufacture of Privigen (immune globulin intravenous) are tested using FDA-licensed serological assays for hepatitis B surface antigen and antibodies to HCV and HIV- as well as FDA-licensed Nucleic Acid Testing (NAT) for HCV and HIV-1 and found to be nonreactive (negative). For HBV, an investigational NAT procedure is used and the plasma units found to be negative; however, the significance of a negative result has not been established.

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MEDICAL ALERT: Your condition can cause complications in a medical emergency. For enrollment information call MedicAlert at 1-800-854-1166 (USA) or 1-800-668-1507 (Canada).

Your child should not receive a booster vaccine if he or she had a life-threatening allergic reaction after the first shot.

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