Celsunax Eiropas Savienība - īslandiešu - EMA (European Medicines Agency)

celsunax

pinax pharma gmbh - ioflupane (123i) - radionuclide imaging; dementia; movement disorders - greining geislavirkja - Þetta lyf er eingöngu ætlað til greiningar. celsunax is indicated for detecting loss of functional dopaminergic neuron terminals in the striatum:in adult patients with clinically uncertain parkinsonian syndromes, for example those with early symptoms, in order to help differentiate essential tremor from parkinsonian syndromes related to idiopathic parkinson’s disease, multiple system atrophy and progressive supranuclear palsy.  celsunax is unable to discriminate between parkinson's disease, multiple system atrophy and progressive supranuclear palsy. Í fullorðinn sjúklingar, til að hjálpa greina líklega með heilabilun lewy líkama frá alzheimer.  celsunax is unable to discriminate between dementia with lewy bodies and parkinson’s disease dementia.

Kirsty (previously Kixelle) Eiropas Savienība - īslandiešu - EMA (European Medicines Agency)

kirsty (previously kixelle)

biosimilar collaborations ireland limited - insúlín aspart - sykursýki - lyf notuð við sykursýki - kirsty is indicated for treatment of diabetes mellitus in adults, adolescents and children aged 1 year and above.

Riltrava Aerosphere Eiropas Savienība - īslandiešu - EMA (European Medicines Agency)

riltrava aerosphere

astrazeneca ab - budesonide, formoterol fumarate dihydrate, glycopyrronium bromide - lungnasjúkdómur, langvarandi hindrandi - lyf til veikindi öndunarvegi sjúkdómum, - riltrava aerosphere is indicated as a maintenance treatment in adult patients with moderate to severe chronic obstructive pulmonary disease (copd) who are not adequately treated by a combination of an inhaled corticosteroid and a long-acting beta2 agonist or combination of a long-acting beta2 agonist and a long-acting muscarinic antagonist (for effects on symptoms control and prevention of exacerbations see section 5.

Roctavian Eiropas Savienība - īslandiešu - EMA (European Medicines Agency)

roctavian

biomarin international limited - valoctocogene roxaparvovec - antihemorrhagics - treatment of severe haemophilia a (congenital factor viii deficiency) in adult patients without a history of factor viii inhibitors and without detectable antibodies to adeno-associated virus serotype 5 (aav5).

Lomudal Augndropar, lausn 20 mg/ml Īslande - īslandiešu - LYFJASTOFNUN (Icelandic Medicines Agency)

lomudal augndropar, lausn 20 mg/ml

stada arzneimittel ag - sodium cromoglicate - augndropar, lausn - 20 mg/ml

Lioresal Stungulyf/innrennslislyf, lausn 0,5 mg/ml Īslande - īslandiešu - LYFJASTOFNUN (Icelandic Medicines Agency)

lioresal stungulyf/innrennslislyf, lausn 0,5 mg/ml

novartis healthcare a/s - baclofenum inn - stungulyf/innrennslislyf, lausn - 0,5 mg/ml

Lioresal Stungulyf/innrennslislyf, lausn 2 mg/ml Īslande - īslandiešu - LYFJASTOFNUN (Icelandic Medicines Agency)

lioresal stungulyf/innrennslislyf, lausn 2 mg/ml

novartis healthcare a/s - baclofenum inn - stungulyf/innrennslislyf, lausn - 2 mg/ml

Lioresal Stungulyf/innrennslislyf, lausn 50 míkróg/ml Īslande - īslandiešu - LYFJASTOFNUN (Icelandic Medicines Agency)

lioresal stungulyf/innrennslislyf, lausn 50 míkróg/ml

novartis healthcare a/s - baclofenum inn - stungulyf/innrennslislyf, lausn - 50 míkróg/ml