dacepton 5 mg/ml infusionsvätska, lösning
ever neuro pharma gmbh - apomorfinhydrokloridhemihydrat - infusionsvätska, lösning - 5 mg/ml - apomorfinhydrokloridhemihydrat 5 mg aktiv substans; natriummetabisulfit hjälpämne - apomorfin
japol orala droppar, lösning
salus haus gmbh & co kg - myntaolja, delvis avmentoliserad - orala droppar, lösning - myntaolja, delvis avmentoliserad 10 ml aktiv substans - medel vid funktionella mag-tarmsymtom
zolsketil pegylated liposomal
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.
celdoxome pegylated liposomal
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).
dacepton 10 mg/ml injektions-/infusionsvätska, lösning
ever neuro pharma gmbh - apomorfinhydrokloridhemihydrat - injektions-/infusionsvätska, lösning - 10 mg/ml - apomorfinhydrokloridhemihydrat 10 mg aktiv substans; natriummetabisulfit hjälpämne - apomorfin
buprenorphine g.l. pharma 2 mg resoriblett, sublingual
g.l. pharma gmbh - buprenorfinhydroklorid - resoriblett, sublingual - 2 mg - buprenorfinhydroklorid 2,16 mg aktiv substans; mannitol hjälpämne; laktosmonohydrat hjälpämne - buprenorfin
buprenorphine g.l. pharma 4 mg resoriblett, sublingual
g.l. pharma gmbh - buprenorfinhydroklorid - resoriblett, sublingual - 4 mg - mannitol hjälpämne; laktosmonohydrat hjälpämne; buprenorfinhydroklorid 4,32 mg aktiv substans - buprenorfin
buprenorphine g.l. pharma 8 mg resoriblett, sublingual
g.l. pharma gmbh - buprenorfinhydroklorid - resoriblett, sublingual - 8 mg - laktosmonohydrat hjälpämne; mannitol hjälpämne; buprenorfinhydroklorid 8,64 mg aktiv substans - buprenorfin
riastap 1 g pulver till injektions-/infusionsvätska, lösning
csl behring gmbh - fibrinogen, humant - pulver till injektions-/infusionsvätska, lösning - 1 g - fibrinogen, humant 1000 mg aktiv substans - humant
fluconazol krka 100 mg kapsel, hård
krka sverige ab - flukonazol - kapsel, hård - 100 mg - natriumlaurilsulfat hjälpämne; flukonazol 100 mg aktiv substans; laktosmonohydrat hjälpämne - flukonazol