Sporimune vet. (Sporimune) Mixtúra, lausn 50 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

sporimune vet. (sporimune) mixtúra, lausn 50 mg/ml

le vet beheer b.v. - ciclosporinum inn - mixtúra, lausn - 50 mg/ml

Equibactin vet. Pasta til inntöku 333 mg/g + 67 mg/g Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

equibactin vet. pasta til inntöku 333 mg/g + 67 mg/g

le vet b.v.* - trimethoprimum inn; sulfadiazinum inn - pasta til inntöku - 333 mg/g + 67 mg/g

Nerfasin vet. Stungulyf, lausn 100 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

nerfasin vet. stungulyf, lausn 100 mg/ml

le vet b.v.* - xylazinum hýdróklóríð - stungulyf, lausn - 100 mg/ml

Nerfasin vet. Stungulyf, lausn 20 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

nerfasin vet. stungulyf, lausn 20 mg/ml

le vet b.v.* - xylazinum hýdróklóríð - stungulyf, lausn - 20 mg/ml

Dimethyl fumarate Neuraxpharm Evrópusambandið - íslenska - EMA (European Medicines Agency)

dimethyl fumarate neuraxpharm

laboratorios lesvi s.l. - dímetýl fúmarat - heila-og mænusigg, köstum tilkynnt - Ónæmisbælandi lyf - dimethyl fumarate neuraxpharma is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Dimethyl fumarate Mylan Evrópusambandið - íslenska - EMA (European Medicines Agency)

dimethyl fumarate mylan

mylan ireland limited - dímetýl fúmarat - heila-og mænusigg, köstum tilkynnt - Ónæmisbælandi lyf - dimethyl fumarate mylan is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Dimethyl fumarate Polpharma Evrópusambandið - íslenska - EMA (European Medicines Agency)

dimethyl fumarate polpharma

zaklady farmafarmaceutyczne polpharma s.aceutyczne polpharma s.a. - dímetýl fúmarat - heila-og mænusigg, köstum tilkynnt - Ónæmisbælandi lyf - dimethyl fumarate polpharma is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Dimethyl fumarate Teva Evrópusambandið - íslenska - EMA (European Medicines Agency)

dimethyl fumarate teva

teva gmbh - dímetýl fúmarat - multiple sclerosis, relapsing-remitting; multiple sclerosis - Ónæmisbælandi lyf - dimethyl fumarate teva is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).

Dimethyl fumarate Accord Evrópusambandið - íslenska - EMA (European Medicines Agency)

dimethyl fumarate accord

accord healthcare s.l.u. - dímetýl fúmarat - multiple sclerosis, relapsing-remitting; multiple sclerosis - Ónæmisbælandi lyf - dimethyl fumarate accord is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).

Clopidogrel Qualimed Evrópusambandið - íslenska - EMA (European Medicines Agency)

clopidogrel qualimed

qualimed - clopidogrel (as hydrochloride) - peripheral vascular diseases; stroke; myocardial infarction - blóðþurrðandi lyf - eða er ætlað í fullorðnir til að fyrirbyggja atherothrombotic atburðum í:sjúklingar sem þjáist af kransæðastíflu (frá nokkrum dögum fyrr en minna en 35 dögum), blóðþurrðar heilablóðfall (frá 7 daga þar til að minna en 6 mánuðum) eða komið útlæga slagæð sjúkdómur. nánari upplýsingar er að vísa til kafla 5.