Uniunea Europeană - suedeză - EMA (European Medicines Agency)

baxter holding b.v. - doxorubicinhydroklorid - sarcoma, kaposi; multiple myeloma; ovarian neoplasms; breast neoplasms - antineoplastiska medel - caelyx pegylerat liposomala anges:som monoterapi för patienter med metastaserad bröstcancer, där det finns en ökad risk för hjärt -; för behandling av framskriden äggstockscancer hos kvinnor som har misslyckats med en första linje platinum-baserad kemoterapi behandling, i kombination med bortezomib för behandling av progressiv multipelt myelom hos patienter som har fått minst en tidigare behandling och som redan har genomgått eller är olämpliga för benmärgstransplantation, för behandling av aids-relaterat kaposis sarkom (ks) i patienter med låga cd4 räknas (.

Uniunea Europeană - suedeză - EMA (European Medicines Agency)

accord healthcare s.l.u. - doxorubicin hydrochloride, liposomal - ovarian neoplasms; sarcoma, kaposi; multiple myeloma - doxorubicin - zolsketil pegylated liposomal is a medicine used to treat the following types of cancer in adults:• breast cancer that has spread to other parts of the body in patients at risk of heart problems. zolsketil pegylated liposomal is used on its own for this disease;• advanced ovarian cancer in women whose previous treatment including a platinum-based cancer medicine has stopped working;• multiple myeloma (a cancer of the white blood cells in the bone marrow), in patients with progressive disease who have received at least one other treatment in the past and have already had, or are unsuitable for, a bone marrow transplantation. zolsketil pegylated liposomal is used in combination with bortezomib (another cancer medicine);• kaposi’s sarcoma in patients with aids who have a very damaged immune system. kaposi’s sarcoma is a cancer that causes abnormal tissue to grow under the skin, on moist body surfaces or on internal organs. zolsketil pegylated liposomal contains the active substance doxorubicin and is a ‘hybrid medicine’. this means that it is similar to a ‘reference medicine’ containing the same active substance called adriamycin. however, in zolsketil pegylated liposomal the active substance is enclosed in tiny fatty spheres called liposomes, whereas this is not the case for adriamycin.

Uniunea Europeană - suedeză - EMA (European Medicines Agency)

yes pharmaceutical development services gmbh - doxorubicinhydroklorid - breast neoplasms; ovarian neoplasms; multiple myeloma; sarcoma, kaposi - antineoplastiska medel - 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).

Suedia - suedeză - Läkemedelsverket (Medical Products Agency)

octapharma ab - koagulationsfaktor viii, human; von willebrandfaktor, human - pulver och vätska till injektionsvätska, lösning - 1000 ie vwf/1000 ie fviii - sackaros hjälpämne; koagulationsfaktor viii, human 1000 ie aktiv substans; von willebrandfaktor, human 1000 ie aktiv substans - von willebrandfaktor och koagulationsfaktor viii i kombination

Suedia - suedeză - Läkemedelsverket (Medical Products Agency)

octapharma ab - koagulationsfaktor viii, human; von willebrandfaktor, human - pulver och vätska till injektionsvätska, lösning - 500 ie vwf/500 ie fviii - von willebrandfaktor, human 500 ie aktiv substans; sackaros hjälpämne; koagulationsfaktor viii, human 500 ie aktiv substans - von willebrandfaktor och koagulationsfaktor viii i kombination

Suedia - suedeză - Läkemedelsverket (Medical Products Agency)

le vet beheer b.v. - klenbuterolhydroklorid - sirap - 25 mikrogram/ml - etanol, vattenfri hjälpämne; klenbuterolhydroklorid 25 mikrog aktiv substans; propylparahydroxibensoat hjälpämne; sackaros hjälpämne; glycerol 85% hjälpämne; metylparahydroxibensoat hjälpämne - klenbuterol - häst

Uniunea Europeană - suedeză - EMA (European Medicines Agency)

les laboratoires servier - irinotecan anhydrous free-base - bukspottskörtelnoplasmer - antineoplastiska medel - behandling av metastatisk adenokarcinom i bukspottkörteln i kombination med 5 fluorouracil (5 fu) och leucovorin (lv) hos vuxna patienter som har utvecklats efter gemcitabinbaserad terapi.

Suedia - suedeză - Läkemedelsverket (Medical Products Agency)

csl behring gmbh - koagulationsfaktor ii, human; koagulationsfaktor ix, human; koagulationsfaktor vii, human; koagulationsfaktor x, human; protein c, humant; protein s, humant - pulver och vätska till injektionsvätska, lösning - 1000 ie - protein s, humant 480 - 1520 ie aktiv substans; heparinnatrium hjälpämne; protein c, humant 600 - 1800 ie aktiv substans; koagulationsfaktor ix, human 800 - 1240 ie aktiv substans; koagulationsfaktor x, human 880 - 2400 ie aktiv substans; koagulationsfaktor vii, human 400 - 1000 ie aktiv substans; koagulationsfaktor ii, human 800 - 1920 ie aktiv substans - vii och x i kombination

Suedia - suedeză - Läkemedelsverket (Medical Products Agency)

orpha-devel handels und vertriebs gmbh - argipressinacetat - koncentrat till infusionsvätska, lösning - 40 ie/2 ml - argipressinacetat 0,147 mg aktiv substans

Suedia - suedeză - Läkemedelsverket (Medical Products Agency)

octapharma ab - koagulationsfaktor viii, human; von willebrandfaktor, human - pulver och vätska till injektionsvätska, lösning - 450 ie fviii / 400 ie vwf - von willebrandfaktor, human 400 ie aktiv substans; koagulationsfaktor viii, human 450 ie aktiv substans; sackaros hjälpämne - von willebrandfaktor och koagulationsfaktor viii i kombination