Nezeril Nefdropar, lausn 0,25 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

nezeril nefdropar, lausn 0,25 mg/ml

perrigo sverige ab - oxymetazolinum hýdróklóríð - nefdropar, lausn - 0,25 mg/ml

Nezeril Nefdropar, lausn 0,5 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

nezeril nefdropar, lausn 0,5 mg/ml

perrigo sverige ab - oxymetazolinum hýdróklóríð - nefdropar, lausn - 0,5 mg/ml

Nezeril Nefúði, lausn 0,25 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

nezeril nefúði, lausn 0,25 mg/ml

perrigo sverige ab - oxymetazolinum hýdróklóríð - nefúði, lausn - 0,25 mg/ml

Nezeril Nefúði, lausn 0,5 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

nezeril nefúði, lausn 0,5 mg/ml

perrigo sverige ab - oxymetazolinum hýdróklóríð - nefúði, lausn - 0,5 mg/ml

ellaOne Evrópusambandið - íslenska - EMA (European Medicines Agency)

ellaone

laboratoire hra pharma - ulipristal - getnaðarvörn, postcoital - hormón kynlíf og stillum á kynfærum kerfi, , neyðarástand getnaðarvarna - neyðartilvikum getnaðarvörn innan 120 klukkustundir (fimm daga) varnarlausa samfarir eða getnaðarvörn bilun.

Dupixent Evrópusambandið - íslenska - EMA (European Medicines Agency)

dupixent

sanofi winthrop industrie - dupilumab - dermatitis, atopic; prurigo; esophageal diseases; asthma; sinusitis - umboðsmenn fyrir húðbólgu, að undanskildu barkstera - atopic dermatitisadults and adolescentsdupixent is indicated for the treatment of moderate-to-severe atopic dermatitis in adults and adolescents 12 years and older who are candidates for systemic therapy. children 6 months to 11 years of agedupixent is indicated for the treatment of severe atopic dermatitis in children 6 months to 11 years old who are candidates for systemic therapy. asthmaadults and adolescentsdupixent is indicated in adults and adolescents 12 years and older as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils and/or raised fraction of exhaled nitric oxide (feno), see section 5. 1, who are inadequately controlled with high dose inhaled corticosteroids (ics) plus another medicinal product for maintenance treatment. children 6 to 11 years of agedupixent is indicated in children 6 to 11 years old as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils and/or raised fraction of exhaled nitric oxide (feno), who are inadequately controlled with medium to high dose inhaled corticosteroids (ics) plus another medicinal product for maintenance treatment. chronic rhinosinusitis with nasal polyposis (crswnp)dupixent is indicated as an add-on therapy with intranasal corticosteroids for the treatment of adults with severe crswnp for whom therapy with systemic corticosteroids and/or surgery do not provide adequate disease control. prurigo nodularis (pn)dupixent is indicated for the treatment of adults with moderate-to-severe prurigo nodularis (pn) who are candidates for systemic therapy. eosinophilic esophagitis (eoe)dupixent is indicated for the treatment of eosinophilic esophagitis in adults and adolescents 12 years and older, weighing at least 40 kg, who are inadequately controlled by, are intolerant to, or who are not candidates for conventional medicinal therapy.

Bluevac BTV (previously known as Bluevac BTV8) Evrópusambandið - íslenska - EMA (European Medicines Agency)

bluevac btv (previously known as bluevac btv8)

cz veterinaria s.a. - bluetongue virus vaccine serotypes 1 or 4 or 8 [inactivated] - Ónæmisfræðilegar upplýsingar - sheep; cattle - sheepactive bólusetningar gegn bluetongue veira serotype 8 til að koma í veg fyrir viraemia og til að draga úr klínískum merki. upphaf ónæmis: 20 dagar eftir annan skammt. lengd ónæmis: 1 ár eftir annan skammt. cattleactive bólusetningar gegn bluetongue veira serotype 8 til að koma í veg fyrir viraemia. upphaf ónæmis: 31 dagar eftir annan skammt. lengd ónæmis: 1 ár eftir annan skammt.

GUDAIR Stungulyf, fleyti ≥ 2 mm ITT avian PPD Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

gudair stungulyf, fleyti ≥ 2 mm itt avian ppd

cz vaccines, s.a.u. - mycobacterium paratuberculosis, inactivated strain 316 f - stungulyf, fleyti - ≥ 2 mm itt avian ppd

Estrogel Hlaup 0,6 mg/g Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

estrogel hlaup 0,6 mg/g

besins healthcare ireland limited - estradiol - hlaup - 0,6 mg/g