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

comtan

orion corporation - entacapone - parkinsonsveiki - anti-parkinsonslyf - skammti er ætlað sem viðbót til að standard undirbúning algengari / benserazide eða algengari / ddc hemli til að nota í fullorðinn sjúklinga með parkinsonsveiki og enda-af-skammt mótor sveiflur, sem ekki er hægt að stöðug á þeim sturtu.

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

comtess

orion corporation - entacapone - parkinsonsveiki - anti-parkinsonslyf - entacapon er ætlað sem viðbót við staðlaða lyfjagjöf levodopa / benserazíðs eða levodopa / carbidopa til notkunar hjá sjúklingum með parkinsonsveiki og skammtahreyfingar í upphafi skammts sem ekki er hægt að koma á stöðugleika á þeim samsetningum.

Entacapone Orion Եվրոպական Միություն - իսլանդերեն - EMA (European Medicines Agency)

entacapone orion

orion corporation - entacapone - parkinsonsveiki - anti-parkinsonslyf - skammti er ætlað sem viðbót til að standard undirbúning algengari / benserazide eða algengari / ddc hemli til að nota í fullorðinn sjúklinga með parkinsonsveiki og enda-af-skammt mótor sveiflur, sem ekki er hægt að stöðug á þeim sturtu.

Spikevax (previously COVID-19 Vaccine Moderna) Եվրոպական Միություն - իսլանդերեն - EMA (European Medicines Agency)

spikevax (previously covid-19 vaccine moderna)

moderna biotech spain, s.l. - single-stranded, 5’-capped messenger rna (mrna) produced using a cell-free in vitro transcription from the corresponding dna templates, encoding the viral spike (s) protein of sars-cov-2 - covid-19 virus infection - bóluefni - spikevax is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older. spikevax bivalent original/omicron ba. 1 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 years of age and older who have previously received at least a primary vaccination course against covid-19. spikevax bivalent original/omicron ba. 4-5 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older.  spikevax xbb. 5 is indicated for active immunisation to prevent covid 19 caused by sars-cov-2 in individuals 6 months of age and older. the use of this vaccine should be in accordance with official recommendations.

Remodulin Innrennslislyf, lausn 1 mg/ml Իսլանդիա - իսլանդերեն - LYFJASTOFNUN (Icelandic Medicines Agency)

remodulin innrennslislyf, lausn 1 mg/ml

ferrer internacional s.a. - treprostinilum natríum - innrennslislyf, lausn - 1 mg/ml

Remodulin Innrennslislyf, lausn 10,0 mg/ml Իսլանդիա - իսլանդերեն - LYFJASTOFNUN (Icelandic Medicines Agency)

remodulin innrennslislyf, lausn 10,0 mg/ml

ferrer internacional s.a. - treprostinilum natríum - innrennslislyf, lausn - 10,0 mg/ml

Remodulin Innrennslislyf, lausn 2,5 mg/ml Իսլանդիա - իսլանդերեն - LYFJASTOFNUN (Icelandic Medicines Agency)

remodulin innrennslislyf, lausn 2,5 mg/ml

ferrer internacional s.a. - treprostinilum natríum - innrennslislyf, lausn - 2,5 mg/ml

Remodulin Innrennslislyf, lausn 5,0 mg/ml Իսլանդիա - իսլանդերեն - LYFJASTOFNUN (Icelandic Medicines Agency)

remodulin innrennslislyf, lausn 5,0 mg/ml

ferrer internacional s.a. - treprostinilum natríum - innrennslislyf, lausn - 5,0 mg/ml

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

beromun

belpharma s.a. - tasonermin - sarkmein - Ónæmisörvandi, - beromun er ætlað í fullorðnir sem viðbót í aðgerð fyrir brottnám æxli svo eins og að koma í veg eða tefja aflimunar, eða í líknandi ástandi, til irresectable mjúk-vefjum sarkmein af útlimum, notuð í ásamt melfalan gegnum vægt hyperthermic einangrað-útlim gegnflæði (ilp).