Cabazitaxel "Medac" 20 mg/ml koncentrat til infusionsvæske, opløsning Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

cabazitaxel "medac" 20 mg/ml koncentrat til infusionsvæske, opløsning

medac gesellschaft für klinische spezialpräparate mbh - cabazitaxel - koncentrat til infusionsvæske, opløsning - 20 mg/ml

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

cabazitaxel teva

teva b.v. - cabazitaxel - prostatiske neoplasmer - antineoplastiske midler - behandling af prostatakræft.

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

jevtana

sanofi winthrop industrie - cabazitaxel - prostatiske neoplasmer - antineoplastiske midler - jevtana i kombination med prednison eller prednisolon er indiceret til behandling af patienter med hormon-ildfast metastatisk prostatacancer, der tidligere er behandlet med en docetaxelholdig behandling.

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

xtandi

astellas pharma europe b.v. - enzalutamide - prostatiske neoplasmer - endokrine terapi - xtandi is indicated for:the treatment of adult men with metastatic hormone-sensitive prostate cancer (mhspc) in combination with androgen deprivation therapy (see section 5. the treatment of adult men with high-risk non-metastatic castration-resistant prostate cancer (crpc) (see section 5. the treatment of adult men with metastatic crpc who are asymptomatic or mildly symptomatic after failure of androgen deprivation therapy in whom chemotherapy is not yet clinically indicated (see section 5. the treatment of adult men with metastatic crpc whose disease has progressed on or after docetaxel therapy.

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

ketoconazole hra

hra pharma rare diseases - ketoconazol - cushing syndrome - antimykotika til systemisk brug - ketoconazol hra er indiceret til behandling af endogent cushings syndrom hos voksne og unge over 12 år.

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

tafinlar

novartis europharm limited - dabrafenib mesilate - melanom - antineoplastiske midler - melanomadabrafenib as monotherapy or in combination with trametinib is indicated for the treatment of adult patients with unresectable or metastatic melanoma with a braf v600 mutation (see sections 4. 4 og 5. adjuverende behandling af melanomadabrafenib i kombination med trametinib er angivet for den adjuverende behandling af voksne patienter med stadium iii melanom med en braf v600 mutation, efter komplet resektion. non-small cell lung cancer (nsclc)dabrafenib in combination with trametinib is indicated for the treatment of adult patients with advanced non-small cell lung cancer with a braf v600 mutation.