Penthrox Innöndunargufa, gegndreyptur stabbi 3 ml Islanda - Iżlandiż - LYFJASTOFNUN (Icelandic Medicines Agency)

penthrox innöndunargufa, gegndreyptur stabbi 3 ml

medical developments ned b.v. - methoxyflurane - innöndunargufa, gegndreyptur stabbi - 3 ml

SevoFlo Unjoni Ewropea - Iżlandiż - EMA (European Medicines Agency)

sevoflo

zoetis belgium sa - sevofluran - deyfilyf, hershöfðingi - dogs; cats - til að framkalla og viðhald í svæfingu hundar og kettir.

Sevohale (previously known as Sevocalm) Unjoni Ewropea - Iżlandiż - EMA (European Medicines Agency)

sevohale (previously known as sevocalm)

chanelle pharmaceuticals manufacturing limited - sevofluran - deyfilyf, hershöfðingi - dogs; cats - til að framkalla og viðhalda svæfingu.

Neuraceq Unjoni Ewropea - Iżlandiż - EMA (European Medicines Agency)

neuraceq

life molecular imaging gmbh - florbetaben (18f) - radionuclide imaging; alzheimer disease - greining geislavirkja - Þetta lyf er eingöngu ætlað til greiningar. neuraceq er radiopharmaceutical fram í sneiðmyndatöku losun höfði (gÆludÝr) hugsanlegur beta amyloid neuritic sýklum þéttleika í heila fullorðinn sjúklinga með vitsmunalegum skert sem eru metin fyrir alzheimer (ad) og aðrar ástæður vitsmunalegum skert. neuraceq ætti að vera notuð í tengslum við mat klínískum. neikvæð skanna sýnir dreifður eða enginn skellum, sem er ekki í samræmi við greiningu á ad.

Padcev Unjoni Ewropea - Iżlandiż - EMA (European Medicines Agency)

padcev

astellas pharma europe b.v. - enfortumab vedotin - carcinoma, transitional cell; urologic neoplasms - Æxlishemjandi lyf - padcev as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic urothelial cancer who have previously received a platinum-containing chemotherapy and a programmed death receptor 1 or programmed death ligand 1 inhibitor.

Roctavian Unjoni Ewropea - Iżlandiż - 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).

Vyvgart Unjoni Ewropea - Iżlandiż - EMA (European Medicines Agency)

vyvgart

argenx - efgartigimod alfa - myasthenia gravis - Ónæmisbælandi lyf - vyvgart is indicated as an add on to standard therapy for the treatment of adult patients with generalised myasthenia gravis (gmg) who are anti acetylcholine receptor (achr) antibody positive.

Opnol Augndropar, lausn 1 mg/ml Islanda - Iżlandiż - LYFJASTOFNUN (Icelandic Medicines Agency)

opnol augndropar, lausn 1 mg/ml

karo pharma ab* - dexamethasonum fosfat - augndropar, lausn - 1 mg/ml