• Home
  • A-B index
  • Pharmacological Index
  • Drug Classes
  • Active Ingredients
  • Companies
  • News
  • Difolta
    / Rafa


    Active Ingredient
    Pralatrexate 20 mg/ml

    Status in Israel
    RX

    Presentation and Status in Health Basket

    Presentation Basket Yarpa Pharmasoft

    Solution for Injection

    1 x 20 mg/ml

    partial basket chart 40912 22363

    Related information


    Indications

    Treatment of relapsed or refractory peripheral T cell lymphoma (PTCL).


    Contra-Indications

    None.


    Special Precautions

    Patients should be instructed to receive folic acid and receive B12. Caution advised in moderate to severe renal impairment. Monitor patients for liver function. May suppress bone marrow function, cause mucositis, severe dermatological reactions, tumor lysis syndrome, liver toxicity. No experience in pediatric use.
    See prescribing information for full details.


    Side Effects

    Most common: mucositis, thrombocytopenia, nausea, and fatigue.
    See prescribing information for full details.

     


    Drug interactions

    Co-administration of increasing doses of probenecid resulted in delayed clearance of pralatrexate and a commensurate increase in exposure. When administering Difolta to patients receiving probenecid or other drugs that may affect relevant transporter systems (e.g., NSAIDs), monitor patients closely for signs of systemic toxicity due to increased drug exposure.


    Pregnancy and Lactation

    Pregnancy: Pregnancy category D.
    Lactation: Not advised during nursing.


    Manufacturer
    Brecon Pharmaceuticals
    CLOSE