الاتحاد الأوروبي - الأيسلاندية - EMA (European Medicines Agency)

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.

الاتحاد الأوروبي - الأيسلاندية - EMA (European Medicines Agency)

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.

أيسلندا - الأيسلاندية - LYFJASTOFNUN (Icelandic Medicines Agency)

krka, d.d., novo mesto - tramadolum hýdróklóríð - forðatafla - 200 mg

أيسلندا - الأيسلاندية - LYFJASTOFNUN (Icelandic Medicines Agency)

upjohn eesv - eletriptanum brómíð - filmuhúðuð tafla - 40 mg

أيسلندا - الأيسلاندية - LYFJASTOFNUN (Icelandic Medicines Agency)

krka, d.d., novo mesto - tramadolum hýdróklóríð - forðatafla - 100 mg

أيسلندا - الأيسلاندية - LYFJASTOFNUN (Icelandic Medicines Agency)

krka, d.d., novo mesto - tramadolum hýdróklóríð - forðatafla - 150 mg

الاتحاد الأوروبي - الأيسلاندية - EMA (European Medicines Agency)

janssen-cilag international n.v. - abiraterone acetate, niraparib tosilate monohydrate - stækkun Æxli, gelding-Þola - Æxlishemjandi lyf - treatment of adult patients with prostate cancer.

أيسلندا - الأيسلاندية - LYFJASTOFNUN (Icelandic Medicines Agency)

stada arzneimittel ag - abirateronum acetat - filmuhúðuð tafla - 500 mg

الاتحاد الأوروبي - الأيسلاندية - EMA (European Medicines Agency)

sanofi-aventis deutschland gmbh - leflúnómíð - arthritis, rheumatoid; arthritis, psoriatic - Ónæmisbælandi lyf - leflúnómíð er ætlað fyrir meðferð fullorðinn sjúklinga með:virk liðagigt sem 'sjúkdómur-að breyta verkjalyf eiturlyf' (dmard);virk psoriasis liðagigt. undanförnum eða samhliða meðferð með lifur eða haematotoxic sjúkdómstemprandi (e. stendur) getur leitt til aukinnar hættu alvarleg neikvæð viðbrögð; því upphaf leflúnómíð meðferð hefur verið vandlega um þetta gagnast / hættu þætti. Þar að auki, skipta úr leflúnómíð til annars dmard án eftir washout aðferð geta líka aukið hættuna af alvarlegum neikvæð viðbrögð jafnvel í langan tíma eftir að skipta.

الاتحاد الأوروبي - الأيسلاندية - EMA (European Medicines Agency)

sanofi winthrop industrie - teriflunomide - margvísleg sclerosis - valdar ónæmisbælandi lyf - aubagio is indicated for the treatment of adult patients and paediatric patients aged 10 years and older with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 for important information on the population for which efficacy has been established).