Imbruvica Evropská unie - norština - 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.

Venclyxto 10 mg Norsko - norština - Statens legemiddelverk

venclyxto 10 mg

abacus medicine a/s - venetoklaks - tablett, filmdrasjert - 10 mg

Venclyxto 50 mg Norsko - norština - Statens legemiddelverk

venclyxto 50 mg

abacus medicine a/s - venetoklaks - tablett, filmdrasjert - 50 mg

Venclyxto 100 mg Norsko - norština - Statens legemiddelverk

venclyxto 100 mg

abacus medicine a/s - venetoklaks - tablett, filmdrasjert - 100 mg

Bendamustine Accord 2.5 mg/ ml Norsko - norština - Statens legemiddelverk

bendamustine accord 2.5 mg/ ml

accord healthcare b.v. - bendamustinhydrokloridmonohydrat - pulver til konsentrat til infusjonsvæske, oppløsning - 2.5 mg/ ml

Levact 2.5 mg/ ml Norsko - norština - Statens legemiddelverk

levact 2.5 mg/ ml

astellas pharma gmbh (1) - bendamustinhydroklorid - pulver til konsentrat til infusjonsvæske, oppløsning - 2.5 mg/ ml

Polivy Evropská unie - norština - EMA (European Medicines Agency)

polivy

roche registration gmbh - polatuzumab vedotin - lymfom, b-celle - antineoplastiske midler - polivy i kombinasjon med bendamustine og rituximab er indisert for behandling av voksne pasienter med tilbakefall/ildfast diffuse store b-celle lymfom (dlbcl) som ikke er kandidater for haematopoietic stamcelletransplantasjon. polivy in combination with rituximab, cyclophosphamide, doxorubicin, and prednisone (r-chp) is indicated for the treatment of adult patients with previously untreated diffuse large b-cell lymphoma (dlbcl).