Lenalidomide Grindeks 5 mg Norveška - norveščina - Statens legemiddelverk

lenalidomide grindeks 5 mg

grindeks as - lenalidomideammoniumklorid - kapsel, hard - 5 mg

Lenalidomide Grindeks 10 mg Norveška - norveščina - Statens legemiddelverk

lenalidomide grindeks 10 mg

grindeks as - lenalidomideammoniumklorid - kapsel, hard - 10 mg

Lenalidomide Grindeks 15 mg Norveška - norveščina - Statens legemiddelverk

lenalidomide grindeks 15 mg

grindeks as - lenalidomideammoniumklorid - kapsel, hard - 15 mg

Lenalidomide Grindeks 20 mg Norveška - norveščina - Statens legemiddelverk

lenalidomide grindeks 20 mg

grindeks as - lenalidomideammoniumklorid - kapsel, hard - 20 mg

Ivemend Evropska unija - norveščina - EMA (European Medicines Agency)

ivemend

merck sharp & dohme b.v. - fosaprepitant - vomiting; cancer - antiemetika og antinauseants, - forebygging av kvalme og oppkast forbundet med svært høy og moderat emetogenic kreft, kjemoterapi, i voksne og paediatric pasienter i alderen 6 måneder og eldre. ivemend 150 mg er gitt som en del av en kombinasjon terapi.

Yondelis Evropska unija - norveščina - EMA (European Medicines Agency)

yondelis

pharma mar s.a. - trabectedin - ovarian neoplasms; sarcoma - antineoplastiske midler - yondelis er indisert for behandling av pasienter med avansert mykosvikt sarkom, etter at antracykliner og ifosfamid har sviktet, eller som ikke er egnet til å motta disse midlene. effekten dataene er basert på liposarcoma og leiomyosarcoma pasienter. yondelis i kombinasjon med pegylated liposomal doxorubicin (pld) er indisert for behandling av pasienter med tilbakefall platinum-sensitive eggstokkreft.

Vidalta vet 15 mg Norveška - norveščina - Statens legemiddelverk

vidalta vet 15 mg

intervet international bv - 5831 an - karbimazol - depottablett - 15 mg

Vidalta vet 10 mg Norveška - norveščina - Statens legemiddelverk

vidalta vet 10 mg

intervet international bv - 5831 an - karbimazol - depottablett - 10 mg

Emgality Evropska unija - norveščina - EMA (European Medicines Agency)

emgality

eli lilly nederland b.v. - galcanezumab - migrene lidelser - analgesics, galcanezumab - emgality er indisert for profylakse av migrene hos voksne som har minst 4 migrene dager per måned.

Zolsketil pegylated liposomal Evropska unija - norveščina - EMA (European Medicines Agency)

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.