Abiraterone Mylan Euroopa Liit - islandi - EMA (European Medicines Agency)

abiraterone mylan

mylan ireland limited - abirateron asetat - blöðruhálskirtli - 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 Euroopa Liit - islandi - EMA (European Medicines Agency)

abiraterone krka

krka, d.d., novo mesto - abirateron asetat - blöðruhálskirtli - innkirtla meðferð - 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.

Lutetium (177Lu) chloride Billev (previously Illuzyce) Euroopa Liit - islandi - EMA (European Medicines Agency)

lutetium (177lu) chloride billev (previously illuzyce)

billev pharma aps - lutetium (177lu) chloride - radionuclide imaging - heilsueyðandi lyf - lutetium (177lu) chloride billev is a radiopharmaceutical precursor, and it is not intended for direct use in patients. it is to be used only for the radiolabelling of carrier molecules that have been specifically developed and authorised for radiolabelling with lutetium (177lu) chloride.

Omnic Hart hylki með breyttan losunarhraða 0,4 mg Island - islandi - LYFJASTOFNUN (Icelandic Medicines Agency)

omnic hart hylki með breyttan losunarhraða 0,4 mg

astellas pharma a/s* - tamsulosinum hýdróklóríð - hart hylki með breyttan losunarhraða - 0,4 mg

Atrovent Lausn í eimgjafa 0,25 mg/ml Island - islandi - LYFJASTOFNUN (Icelandic Medicines Agency)

atrovent lausn í eimgjafa 0,25 mg/ml

boehringer ingelheim international gmbh* - ipratropii bromidum inn - lausn í eimgjafa - 0,25 mg/ml

Atrovent Innúðalyf, lausn 20 míkróg/skammt Island - islandi - LYFJASTOFNUN (Icelandic Medicines Agency)

atrovent innúðalyf, lausn 20 míkróg/skammt

boehringer ingelheim international gmbh* - ipratropii bromidum inn - innúðalyf, lausn - 20 míkróg/skammt

Cutaquig Stungulyf, lausn 165 mg/ml Island - islandi - LYFJASTOFNUN (Icelandic Medicines Agency)

cutaquig stungulyf, lausn 165 mg/ml

octapharma ab - immunoglobulinum humanum inn - stungulyf, lausn - 165 mg/ml