Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

octapharma ab - koagulationsfaktor viii, humant, von willebrand faktor, human - pulver og solvens til injektionsvæske, opløsning - 1000 ie+1000 ie

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

octapharma ab - koagulationsfaktor viii, humant, von willebrand faktor, human - pulver og solvens til injektionsvæske, opløsning - 500 ie+500 ie

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

paranova danmark a/s - methylprednisolonnatriumsuccinat - pulver og solvens til injektionsvæske, opløsning - 125 mg

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

paranova danmark a/s - hydrocortisonnatriumsuccinat - pulver og solvens til injektionsvæske, opløsning - 100 mg

Den Europæiske Union - dansk - EMA (European Medicines Agency)

baxter holding b.v. - doxorubicinhydrochlorid - sarcoma, kaposi; multiple myeloma; ovarian neoplasms; breast neoplasms - antineoplastiske midler - caelyx pegyleret liposomal er anført:som monoterapi til patienter med metastatisk brystkræft, hvor der er en øget cardiac risiko;til behandling af fremskreden kræft i æggestokkene hos kvinder, der har undladt en første linje platin-baseret kemoterapi, og i kombination med bortezomib til behandling af progressive myelomatose patienter, der har modtaget mindst én tidligere behandling, og som allerede har gennemgået eller er uegnet for bone marrow transplantation;til behandling af aids-relateret kaposis sarkom (ks) i patienter med lavt cd4-tæller (.

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

paranova danmark a/s - lanthanumcarbonathydrat - tyggetabletter - 1000 mg

Den Europæiske Union - dansk - EMA (European Medicines Agency)

teva pharma b.v. - mycophenolatmofetil - graft afvisning - immunosuppressiva - mycophenolatmofetil teva angives i kombination med ciclosporin og kortikosteroider til forebyggelse af akutte transplantation afvisning i patienter, allogen nyre, hjerte eller hepatisk transplantationer.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

accord healthcare s.l.u. - dabigatran etexilate mesilate - venous thromboembolism; arthroplasty, replacement - antitrombotiske midler - prevention of venous thromboembolic events.

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

medac gesellschaft für klinische - dacarbazincitrat - pulver til infusionsvæske, opløsning - 1000 mg

Den Europæiske Union - dansk - 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.