Bevacizumab

    Bevacizumab — package

    info General information

    Name Bevacizumab, 25 mg/mL, concentrate for solution for infusion
    INN Bevacizumab
    Active substance Bevacizumab
    Pharmacotherapeutic group Antineoplastic agents. Monoclonal antibodies and antibody conjugates. VEGF/VEGFR (vascular endothelial growth factor) inhibitors. Bevacizumab
    Dosage form Concentrate for solution for infusion
    Packaging

    4 mL or 16 mL of the product in a vial. 1 vial (4 mL or 16 mL) is placed in a cardboard box.

    Manufacturer Karaganda Pharmaceutical Complex LLP EU GMP

    assignment_turned_in Indications

    Bevacizumab is used to treat adult patients with:

    • advanced colorectal cancer, in combination with fluoropyrimidine-based chemotherapy.
    • metastatic breast cancer, in combination with capecitabine or paclitaxel.
    • non-small cell lung cancer, in combination with platinum-based chemotherapy.
    • advanced non-small cell lung cancer in which the cancer cells have specific mutations of a protein called epidermal growth factor receptor (EGFR). Bevacizumab will be given in combination with erlotinib.
    • kidney cancer, in combination with medicines called interferons.
    • advanced epithelial ovarian, fallopian tube or primary peritoneal cancer, in combination with carboplatin and paclitaxel.
    • advanced epithelial ovarian, fallopian tube or primary peritoneal cancer in which symptoms have returned at least 6 months after the last platinum-based chemotherapy. These patients will receive Bevacizumab in combination with carboplatin and gemcitabine.
    • advanced epithelial ovarian, fallopian tube or primary peritoneal cancer in which symptoms have returned less than 6 months after the last platinum-based chemotherapy. These patients will receive Bevacizumab in combination with paclitaxel, or topotecan, or pegylated liposomal doxorubicin.
    • persistent, recurrent or metastatic cervical cancer, in combination with paclitaxel and cisplatin, or paclitaxel and topotecan if the patient cannot receive platinum therapy.