Nicorette Cooldrops Hörð munnsogstafla 4 mg Իսլանդիա - իսլանդերեն - LYFJASTOFNUN (Icelandic Medicines Agency)

nicorette cooldrops hörð munnsogstafla 4 mg

mcneil denmark aps - nicotinum resin-komplex - hörð munnsogstafla - 4 mg

Pneumovax Stungulyf, lausn í áfylltri sprautu 25 míkróg Իսլանդիա - իսլանդերեն - LYFJASTOFNUN (Icelandic Medicines Agency)

pneumovax stungulyf, lausn í áfylltri sprautu 25 míkróg

merck sharp & dohme b.v. - pneumococcal polysaccharide danish types 1,2,3,4,5,6b,7f,8,9n,9v,10a,11a,12f,14,15b,17f,18,c,19a, 19f,20,22f,23f,33f - stungulyf, lausn í áfylltri sprautu - 25 míkróg

Zoonotic Influenza Vaccine Seqirus Եվրոպական Միություն - իսլանդերեն - EMA (European Medicines Agency)

zoonotic influenza vaccine seqirus

seqirus s.r.l.  - zoonotic influenza vaccine (h5n1) (surface antigen, inactivated, adjuvanted), influenza virus surface antigens (haemagglutinin and neuraminidase) of strain: a/turkey/turkey/1/05 (h5n1)-like strain (nibrg-23) - influenza a virus, h5n1 subtype - bóluefni - active immunisation against h5 subtype of influenza a virus.

Repevax Stungulyf, dreifa áfyllt sprauta Իսլանդիա - իսլանդերեն - LYFJASTOFNUN (Icelandic Medicines Agency)

repevax stungulyf, dreifa áfyllt sprauta

sanofi pasteur* - tetanus toxoid; diphtheria toxoid; pertussis toxoid; filamentous haemagglutinin; pertussis fimbrial agglutinogens (fim) 2 and 3; pertactin; poliovirus (inactivated) type 1 (mahoney strain); poliovirus (inactivated) type 2 (mef-1 strain); poliovirus (inactivated) type 3 (saukett strain) - stungulyf, dreifa - áfyllt sprauta

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

orphacol

theravia - cholic sýru - digestive system diseases; metabolism, inborn errors - galli sýra og afleiður - orphacol er ætlað fyrir meðferð meðfæddan villur í aðal galli-sýru myndun vegna 3β-hýdroxý-Δ5-c27-stera oxidoreductase skort eða Δ4-3-oxosteroid-5β-redúktasa skort á börn, börn og unglingar á aldrinum einn mánuð til 18 ára og fullorðnir.

FOMEPIZOLE SERB (Fomepizole EUSA Pharma) Innrennslisþykkni, lausn 5 mg/ml Իսլանդիա - իսլանդերեն - LYFJASTOFNUN (Icelandic Medicines Agency)

fomepizole serb (fomepizole eusa pharma) innrennslisþykkni, lausn 5 mg/ml

serb s.a. - fomepizolum súlfat - innrennslisþykkni, lausn - 5 mg/ml

Torphadine vet. Stungulyf, lausn 10 mg/ml Իսլանդիա - իսլանդերեն - LYFJASTOFNUN (Icelandic Medicines Agency)

torphadine vet. stungulyf, lausn 10 mg/ml

le vet beheer b.v. - butorphanolum tartrat - stungulyf, lausn - 10 mg/ml

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

vaxchora

bavarian nordic a/s - vibrio cholerae, álag cvd 103-hgr, lifandi - cholera - bóluefni - vaxchora is indicated for active immunisation against disease caused by vibrio cholerae serogroup o1 in adults and children aged 2 years and older. Þetta bóluefni ætti að vera notuð í samræmi við opinbera tillögur.

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

prehevbri

vbi vaccines b.v. - lifrarbólga b yfirborðs mótefnavaka - lifrarbólga b - bóluefni - prehevbri is indicated for active immunisation against infection caused by all known subtypes of the hepatitis b virus in adults. it can be expected that hepatitis d will also be prevented by immunisation with prehevbri as hepatitis d (caused by the delta agent) does not occur in the absence of hepatitis b infection. the use of prehevbri should be in accordance with official recommendations.

Clopidogrel BGR (previously Zylagren) Եվրոպական Միություն - իսլանդերեն - EMA (European Medicines Agency)

clopidogrel bgr (previously zylagren)

biogaran - clopidogrel (as hydrogen sulfate) - peripheral vascular diseases; stroke; myocardial infarction - blóðþurrðandi lyf - fyrirbyggja atherothrombotic atburðum sem eftir er ætlað:fullorðinn 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.