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  • Pomalidomide Teva
    / Teva Israel LTD, Israel


    Active Ingredient
    Pomalidomide 1 mg, 2 mg, 3 mg, 4 mg

    Status in Israel
    RX

    Presentation and Status in Health Basket

    Presentation Basket Yarpa Pharmasoft

    Hard Capsules

    21 x 1 mg

    partial basket chart 69260 24997

    Hard Capsules

    21 x 2 mg

    partial basket chart 69270 24998

    Hard Capsules

    21 x 3 mg

    partial basket chart 69275 5782

    Hard Capsules

    21 x 4 mg

    partial basket chart 69278 5783

    Related information


    Dosage

    Pomalidomide in combination with bortezomib and dexamethasone
    The recommended starting dose of pomalidomide is 4 mg taken orally once daily on Days 1 to 14 of repeated 21-day cycles.
    Treatment with pomalidomide combined with bortezomib and dexamethasone should be given until disease progression or until unacceptable toxicity occurs.
    Pomalidomide in combination with dexamethasone
    The recommended starting dose of pomalidomide is 4 mg taken orally once daily on Days 1 to 21 of each 28-day cycle.
    Treatment with pomalidomide combined with dexamethasone should be given until disease progression or until unacceptable toxicity occurs.
    Please refer to the license holder for further details.


    Indications

    Pomalidomide in combination with dexamethasone
    Treatment of adult patients with relapsed and refractory multiple myeloma who have received at least two prior treatment regimens, including both lenalidomide and bortezomib, and have demonstrated disease progression on the last therapy.
    Pomalidomide in combination with bortezomib and dexamethasone
    Treatment of adult patients with multiple myeloma who have received at least one prior treatment regimen including lenalidomide.


    Contra-Indications

    * Pregnancy.
    * Women of childbearing potential, unless all the conditions of the Imnovid Risk Management Program – Pregnancy Prevention Program (RMP-PPP) are met.
    * Male patients unable to follow or comply with the required contraceptive measures.
    * Hypersensitivity to the active substance or to any of the excipients.


    Special Precautions

    Please refer to the license holder for further details.


    Side Effects

    Please refer to the license holder for further details.


    Drug interactions

    Please refer to the license holder for further details.


    Pregnancy and Lactation

    Please refer to the license holder for further details.


    Overdose

    Please refer to the license holder for further details.

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