Crysvita Եվրոպական Միություն - իսլանդերեն - EMA (European Medicines Agency)

crysvita

kyowa kirin holdings b.v. - burosumab - hypophosphatemia, familial; hypophosphatemic rickets, x-linked dominant; osteomalacia - lyf til að meðhöndla beinsjúkdóma - crysvita is indicated for the treatment of x-linked hypophosphataemia, in children and adolescents aged 1 to 17 years with radiographic evidence of bone disease, and in adults. crysvita is indicated for the treatment of fgf23-related hypophosphataemia in tumour-induced osteomalacia associated with phosphaturic mesenchymal tumours that cannot be curatively resected or localised in children and adolescents aged 1 to 17 years and in adults.

Lupkynis Եվրոպական Միություն - իսլանդերեն - EMA (European Medicines Agency)

lupkynis

otsuka pharmaceutical netherlands b.v. - voclosporin - lupus nephritis - Ónæmisbælandi lyf - lupkynis is indicated in combination with mycophenolate mofetil for the treatment of adult patients with active class iii, iv or v (including mixed class iii/v and iv/v) lupus nephritis (ln).

Acetylcystein Mylan Freyðitafla 200 mg Իսլանդիա - իսլանդերեն - LYFJASTOFNUN (Icelandic Medicines Agency)

acetylcystein mylan freyðitafla 200 mg

mylan ab* - acetylcysteinum inn - freyðitafla - 200 mg

Stamaril Stungulyfsstofn og leysir, dreifa Իսլանդիա - իսլանդերեն - LYFJASTOFNUN (Icelandic Medicines Agency)

stamaril stungulyfsstofn og leysir, dreifa

sanofi pasteur* - gulusóttarveira 17d-204 stofn (lifandi, veikluð) - stungulyfsstofn og leysir, dreifa

Amoxicillin Sandoz Mixtúruduft, dreifa 100 mg/ml Իսլանդիա - իսլանդերեն - LYFJASTOFNUN (Icelandic Medicines Agency)

amoxicillin sandoz mixtúruduft, dreifa 100 mg/ml

sandoz a/s* - amoxicillinum tríhýdrat - mixtúruduft, dreifa - 100 mg/ml

Mucolysin Freyðitafla 600 mg Իսլանդիա - իսլանդերեն - LYFJASTOFNUN (Icelandic Medicines Agency)

mucolysin freyðitafla 600 mg

sandoz a/s* - acetylcysteinum inn - freyðitafla - 600 mg

Calcium Sandoz Freyðitafla 500 mg Իսլանդիա - իսլանդերեն - LYFJASTOFNUN (Icelandic Medicines Agency)

calcium sandoz freyðitafla 500 mg

sandoz a/s - calcii carbonas; calcii lacto-gluconas - freyðitafla - 500 mg

Dolorin Junior Mixtúra, lausn 24 mg/ml Իսլանդիա - իսլանդերեն - LYFJASTOFNUN (Icelandic Medicines Agency)

dolorin junior mixtúra, lausn 24 mg/ml

williams & halls ehf. - paracetamolum inn - mixtúra, lausn - 24 mg/ml

Zofran Mixtúra, lausn 0,8 mg/ml Իսլանդիա - իսլանդերեն - LYFJASTOFNUN (Icelandic Medicines Agency)

zofran mixtúra, lausn 0,8 mg/ml

sandoz a/s - ondansetronum hýdróklóríð - mixtúra, lausn - 0,8 mg/ml

Bekemv Եվրոպական Միություն - իսլանդերեն - EMA (European Medicines Agency)

bekemv

amgen technology (ireland) uc - eculizumab - blóðrauði, ofsakláði - Ónæmisbælandi lyf - bekemv is indicated in adults and children for the treatment of paroxysmal nocturnal haemoglobinuria (pnh). sönnunargögn klínískum gagn er sýnt í sjúklinga með haemolysis með klínískum einkenni(s) marks um hár sjúkdómur starfsemi, óháð blóðgjöf sögu (sjá kafla 5.