Lenalidomide Sandoz 20 mg Norvegija - norvegų - Statens legemiddelverk

lenalidomide sandoz 20 mg

sandoz - københavn - lenalidomid - kapsel, hard - 20 mg

Lenalidomide Sandoz 25 mg Norvegija - norvegų - Statens legemiddelverk

lenalidomide sandoz 25 mg

sandoz - københavn - lenalidomid - kapsel, hard - 25 mg

Lenalidomid Zentiva 2.5 mg Norvegija - norvegų - Statens legemiddelverk

lenalidomid zentiva 2.5 mg

zentiva k.s. - lenalidomid - kapsel, hard - 2.5 mg

Lenalidomid Zentiva 7.5 mg Norvegija - norvegų - Statens legemiddelverk

lenalidomid zentiva 7.5 mg

zentiva k.s. - lenalidomid - kapsel, hard - 7.5 mg

Imbruvica Europos Sąjunga - norvegų - EMA (European Medicines Agency)

imbruvica

janssen-cilag international nv - ibrutinib - lymphoma, mantle-cell; leukemia, lymphocytic, chronic, b-cell - antineoplastic agents, protein kinase inhibitors - imbruvica as a single agent is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (mcl). imbruvica as a single agent or in combination with rituximab or obinutuzumab or venetoclax is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (cll) (see section 5. imbruvica as a single agent or in combination with bendamustine and rituximab (br) is indicated for the treatment of adult patients with cll who have received at least one prior therapy. imbruvica as a single agent is indicated for the treatment of adult patients with waldenström’s macroglobulinaemia (wm) who have received at least one prior therapy, or in first line treatment for patients unsuitable for chemo immunotherapy. imbruvica in combination with rituximab is indicated for the treatment of adult patients with wm.