Mabthera 500 mg concentrate for solution for infusion. Roches mabthera rituximab blood cancer and inflammatory diseases drug faces cheaper competition for the first time in europe after regulators approved. Mabthera 1400 mg solution for subcutaneous injection. Rituximab is a genetically engineered chimeric mousehuman monoclonal antibody. Qualitative and quantitative composition 1 singleuse vial contains 100 mg in 10 ml of rituximab. Statistical process control is not an abstract theoretical exercise for mathematicians. No total, 321 no total, 321 pacientes 162 rcvp, 159 cvp receberam o tratamento e foram analisados quanto a eficacia. Mabthera monotherapy is indicated for treatment of patients with stage iii iv follicular lymphoma who are chemoresistant or are in their second or subsequent relapse after chemotherapy. Click, drag, and drop to reorder files or press delete to remove any content you dont want. Click add files and select the files you want to include in your pdf. Relevant identified uses of the substance or mixture and uses advised against use pharmaceutical active substance antineoplastic 1. Mabthera maintenance therapy is indicated for the treatment of follicular lymphoma patients responding to induction therapy.
Minimization of administration route errors with subcutaneous rituximab article pdf available in journal of oncology pharmacy practice 221 october 2014 with 28 reads how we measure reads. Pdf minimization of administration route errors with. Novartis nvs announced that the ema has accepted its generic arm sandozs maa for its proposed biosimilar of roches rhhby mabthera. Mabthera maintenanc e therapy is indicated for the treatment of follicular lymphoma patients responding to induction therapy. Sukl ensures that all human pharmaceuticals available on the czech market meet appropriate standards of quality, safety and efficiency and only safe and functional medical devices are used. Novartis filing for mabthera biosimilar accepted in the eu.
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