Abiraterone Accord Europeiska unionen - svenska - EMA (European Medicines Agency)

abiraterone accord

accord healthcare s.l.u. - abirateronacetat - prostatiska neoplasmer - endokrin terapi - abiraterone accord is indicated with prednisone or prednisolone for:the treatment of newly diagnosed high risk metastatic hormone sensitive prostate cancer (mhspc) in adult men in combination with androgen deprivation therapy (adt)the treatment of metastatic castration resistant prostate cancer (mcrpc) in adult men who are asymptomatic or mildly symptomatic after failure of androgen deprivation therapy in whom chemotherapy is not yet clinically indicatedthe treatment of mcrpc in adult men whose disease has progressed on or after a docetaxel based chemotherapy regimen.

Abiraterone Mylan Europeiska unionen - svenska - EMA (European Medicines Agency)

abiraterone mylan

mylan ireland limited - abirateronacetat - prostatiska neoplasmer - endocrine therapy, other hormone antagonists and related agents - abiraterone mylan is indicated with prednisone or prednisolone for:the treatment of newly diagnosed high risk metastatic hormone sensitive prostate cancer (mhspc) in adult men in combination with androgen deprivation therapy (adt). the treatment of metastatic castration resistant prostate cancer (mcrpc) in adult men who are asymptomatic or mildly symptomatic after failure of androgen deprivation therapy in whom chemotherapy is not yet clinically indicated. the treatment of mcrpc in adult men whose disease has progressed on or after a docetaxel based chemotherapy regimen.

Abiraterone Krka Europeiska unionen - svenska - EMA (European Medicines Agency)

abiraterone krka

krka, d.d., novo mesto - abirateronacetat - prostatiska neoplasmer - endokrin terapi - abiraterone krka is indicated with prednisone or prednisolone for:the treatment of newly diagnosed high risk metastatic hormone sensitive prostate cancer (mhspc) in adult men in combination with androgen deprivation therapy (adt) (see section 5. 1)the treatment of metastatic castration resistant prostate cancer (mcrpc) in adult men who are asymptomatic or mildly symptomatic after failure of androgen deprivation therapy in whom chemotherapy is not yet clinically indicated (see section 5. 1)the treatment of mcrpc in adult men whose disease has progressed on or after a docetaxel-based chemotherapy regimen.

Amvuttra Europeiska unionen - svenska - EMA (European Medicines Agency)

amvuttra

alnylam netherlands b.v. - vutrisiran sodium - amyloid neuropathies, familial - andra nervsystemet droger - treatment of hereditary transthyretin-mediated amyloidosis (hattr amyloidosis) in adult patients with stage 1 or stage 2 polyneuropathy.

Polyvar 275 mg Bikupestrip Sverige - svenska - Läkemedelsverket (Medical Products Agency)

polyvar 275 mg bikupestrip

bayer animal health gmbh - flumetrin - bikupestrip - 275 mg - flumetrin 275 mg aktiv substans; propylenglykoldikaprylokaprat hjälpämne - bi

Formic acid NOD 68,2 g Bikupestrip Sverige - svenska - Läkemedelsverket (Medical Products Agency)

formic acid nod 68,2 g bikupestrip

nod apiary ireland limited - myrsyra - bikupestrip - 68,2 g - sackaros, flytande hjälpämne; myrsyra 68,2 g aktiv substans - bi

Apiguard vet 12,5 g Gel Sverige - svenska - Läkemedelsverket (Medical Products Agency)

apiguard vet 12,5 g gel

vita bee health limited - tymol - gel - 12,5 g - tymol 12,5 g aktiv substans - tymol - bi

Apiguard vet 12,5 g/dos Bikupegel Sverige - svenska - Läkemedelsverket (Medical Products Agency)

apiguard vet 12,5 g/dos bikupegel

vita bee health limited - tymol - bikupegel - 12,5 g/dos - tymol 12,5 g aktiv substans - bi

Apivar vet 500 mg Bikupestrip Sverige - svenska - Läkemedelsverket (Medical Products Agency)

apivar vet 500 mg bikupestrip

veto-pharma - amitraz - bikupestrip - 500 mg - amitraz 500 mg aktiv substans - bi

Dasatinib Sandoz 20 mg Filmdragerad tablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

dasatinib sandoz 20 mg filmdragerad tablett

sandoz a/s - dasatinib (vattenfri) - filmdragerad tablett - 20 mg - dasatinib (vattenfri) 20 mg aktiv substans; natriumlaurilsulfat hjälpämne; laktosmonohydrat hjälpämne