VPRIV

Generic name: Velaglucerase Alfa
Drug class: Lysosomal enzymes

Usage of VPRIV

VPRIV is a man-made form of an enzyme that occurs naturally in the body in healthy people. Some people lack this enzyme because of a genetic disorder. Vvelaglucerase alfa is used as an enzyme replacement in people with Type I Gaucher disease.

Gaucher disease is a genetic condition in which the body lacks the enzyme needed to break down certain fatty materials (lipids). Lipids can build up in the body, causing symptoms such as easy bruising or bleeding, weakness, anemia, bone or joint pain, enlarged liver or spleen, or weakened bones that are easily fractured.

VPRIV may improve the condition of the liver, spleen, bones, and blood cells in people with Type I Gaucher disease, however, VPRIV is not a cure for this condition.

VPRIV side effects

Get emergency medical help if you have signs of an allergic reaction to VPRIV: hives; fever; chest discomfort, difficult breathing; swelling of your face, lips, tongue, or throat.

An allergic reaction may occur during or shortly after infusion of this medicine. Tell your caregivers or get emergency medical help right away if you have any signs of a severe allergic reaction, such as headache, dizziness, fever, nausea, feeling weak or tired, and feeling like you might pass out.

Common VPRIV side effects may include:

  • headache;
  • dizziness;
  • feeling weak or tired;
  • nausea, stomach pain;
  • joint pain, back pain; or
  • fever.
  • This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

    Before taking VPRIV

    You should not use VPRIV if you are allergic to velaglucerase alfa.

    Tell your doctor if you are pregnant or breastfeeding.

    It is not known whether velaglucerase alfa will harm an unborn baby. However, having untreated Type I Gaucher disease during pregnancy may cause complications such as miscarriage or stillbirth. Type I Gaucher disease also can get worse during pregnancy and may cause medical problems in both mother and baby. The benefit of treating this disease with velaglucerase alfa may outweigh any risks to the baby

    VPRIV is not approved for use by anyone younger than 4 years old.

    Relate drugs

    How to use VPRIV

    Usual Adult Dose for Gaucher Disease:

    Starting dose for patients naive to enzyme replacement therapy (ERT): 60 units/kg IV every other week Switching from imiglucerase to VPRIV: Patients currently being treated with stable doses of imiglucerase may switch by starting this drug at the previous imiglucerase dose 2 weeks after the last imiglucerase dose. Comments: -This drug should be administered as a 60-minute IV infusion under the supervision of a healthcare professional. Use: For long-term ERT for patients with type 1 Gaucher disease

    Usual Pediatric Dose for Gaucher Disease:

    4 years or older: -Starting dose for patients naive to ERT: 60 units/kg IV every other week -Switching from imiglucerase to VPRIV: Patients currently being treated with stable doses of imiglucerase may switch by starting this drug at the previous imiglucerase dose 2 weeks after the last imiglucerase dose. Comments: -This drug should be administered as a 60-minute IV infusion under the supervision of a healthcare professional. Use: For long-term ERT for patients with type 1 Gaucher disease

    Warnings

    Some people receiving a VPRIV injection have had a reaction to the infusion (when the medicine is injected into the vein). Most infusion reactions have been mild. However, tell your caregiver right away if you experionce any of the following symptoms; headache, dizziness, fever, nausea, feeling weak or tired, and feeling like you might pass out. VPRIV is not a cure for Gaucher disease.

    Follow all directions on your medicine label and package. Tell each of your healthcare providers about all your medical conditions, allergies, and all medicines you use.

    What other drugs will affect VPRIV

    Other drugs may interact with velaglucerase alfa, including prescription and over-the-counter medicines, vitamins, and herbal products. Tell each of your health care providers about all medicines you use now and any medicine you start or stop using.

    Disclaimer

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