Bleomycin Baxter 15000 IE Norge - norsk - Statens legemiddelverk

bleomycin baxter 15000 ie

baxter medical ab - bleomycinsulfat - pulver til injeksjons-/infusjonsvæske, oppløsning - 15000 ie

Cisplatin Accord 1 mg/ ml Norge - norsk - Statens legemiddelverk

cisplatin accord 1 mg/ ml

accord healthcare b.v. - cisplatin - konsentrat til infusjonsvæske, oppløsning - 1 mg/ ml

Medisinsk Oksygen Air Liquide 100 % Norge - norsk - Statens legemiddelverk

medisinsk oksygen air liquide 100 %

air liquide santé international - oksygen - medisinsk gass, komprimert - 100 %

Medisinsk Oksygen Air Liquide 100 % Norge - norsk - Statens legemiddelverk

medisinsk oksygen air liquide 100 %

air liquide santé international - oksygen - medisinsk gass, kryogen - 100 %

Celdoxome pegylated liposomal Den europeiske union - norsk - EMA (European Medicines Agency)

celdoxome pegylated liposomal

yes pharmaceutical development services gmbh - doxorubicin hydroklorid - breast neoplasms; ovarian neoplasms; multiple myeloma; sarcoma, kaposi - antineoplastiske midler - celdoxome pegylated liposomal is indicated in adults:as monotherapy for patients with metastatic breast cancer, where there is an increased cardiac risk. or treatment of advanced ovarian cancer in women who have failed a first-line platinum-based chemotherapy regimen. in combination with bortezomib for the treatment of progressive multiple myeloma in patients who have received at least one prior therapy and who have already undergone or are unsuitable for bone marrow transplant. for treatment of aids-related kaposi’s sarcoma (ks) in patients with low cd4 counts (< 200 cd4 lymphocytes/mm3) and extensive mucocutaneous or visceral disease. celdoxome pegylated liposomal may be used as first-line systemic chemotherapy, or as second line chemotherapy in aids-ks patients with disease that has progressed with, or in patients intolerant to, prior combination systemic chemotherapy comprising at least two of the following agents: a vinca alkaloid, bleomycin and standard doxorubicin (or other anthracycline).

Allopurinol Sandoz 100 mg Norge - norsk - Statens legemiddelverk

allopurinol sandoz 100 mg

sandoz - københavn - allopurinol - tablett - 100 mg

Allopurinol Sandoz 300 mg Norge - norsk - Statens legemiddelverk

allopurinol sandoz 300 mg

sandoz - københavn - allopurinol - tablett - 300 mg

Zyloric 100 mg Norge - norsk - Statens legemiddelverk

zyloric 100 mg

aspen pharma trading limited - allopurinol - tablett - 100 mg

Zyloric 300 mg Norge - norsk - Statens legemiddelverk

zyloric 300 mg

aspen pharma trading limited - allopurinol - tablett - 300 mg

Adcetris Den europeiske union - norsk - EMA (European Medicines Agency)

adcetris

takeda pharma a/s - brentuximab vedotin - lymphoma, non-hodgkin; hodgkin disease - antineoplastiske midler - hodgkin lymphomaadcetris is indicated for adult patients with previously untreated cd30+ stage iv hodgkin lymphoma (hl) in combination with doxorubicin, vinblastine and dacarbazine (avd). adcetris is indicated for the treatment of adult patients with cd30+ hl at increased risk of relapse or progression following autologous stem cell transplant (asct). adcetris is indicated for the treatment of adult patients with relapsed or refractory cd30+ hodgkin lymphoma (hl):following asct, orfollowing at least two prior therapies when asct or multi-agent chemotherapy is not a treatment option. systemic anaplastic large cell lymphomaadcetris in combination with cyclophosphamide, doxorubicin and prednisone (chp) is indicated for adult patients with previously untreated systemic anaplastic large cell lymphoma (salcl). adcetris is indicated for the treatment of adult patients with relapsed or refractory salcl. cutaneous t cell lymphomaadcetris is indicated for the treatment of adult patients with cd30+ cutaneous t cell lymphoma (ctcl) after at least 1 prior systemic therapy.