Xtandi Evrópusambandið - íslenska - EMA (European Medicines Agency)

xtandi

astellas pharma europe b.v. - enzalutamíð - blöðruhálskirtli - innkirtla meðferð - 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.

Vanflyta Evrópusambandið - íslenska - EMA (European Medicines Agency)

vanflyta

daiichi sankyo europe gmbh - quizartinib dihydrochloride - kyrningahvítblæði, mergbólga - antineoplastic agents, protein kinase inhibitors - vanflyta is indicated in combination with standard cytarabine and anthracycline induction and standard cytarabine consolidation chemotherapy, followed by vanflyta single-agent maintenance therapy for adult patients with newly diagnosed acute myeloid leukaemia (aml) that is flt3-itd positive.

Vectibix Evrópusambandið - íslenska - EMA (European Medicines Agency)

vectibix

amgen europe b.v. - panitumumab - litlaræxli - Æxlishemjandi lyf - vectibix is indicated for the treatment of adult patients with wild-type ras metastatic colorectal cancer (mcrc): , in first-line in combination with folfox or folfiri. , í öðru-línu í ásamt folfiri fyrir sjúklinga sem hafa fengið fyrsta lína fluoropyrimidine byggir lyfjameðferð (án irínótecan). , eitt og sér eftir bilun fluoropyrimidine-, oxaliplatin-og irínótecan-inniheldur lyfjameðferð meðferð.

Amiloride/HCT Alvogen (Diuramin) Tafla 5/50 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

amiloride/hct alvogen (diuramin) tafla 5/50 mg

alvogen ehf. - amiloridum hýdróklóríð; hydrochlorothiazidum inn - tafla - 5/50 mg

Amiloride/HCT Alvogen (Diuramin mite) Tafla 2,5/25 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

amiloride/hct alvogen (diuramin mite) tafla 2,5/25 mg

alvogen ehf. - amiloridum hýdróklóríð; hydrochlorothiazidum inn - tafla - 2,5/25 mg