Rixubis 유럽 연합 - 노르웨이어 - EMA (European Medicines Agency)

rixubis

baxalta innovations gmbh - nonacog gamma - hemofili b - antihemoragika - behandling og profylakse av blødning hos pasienter med hemofili b (medfødt faktor ix-mangel).

Jorveza 유럽 연합 - 노르웨이어 - EMA (European Medicines Agency)

jorveza

dr. falk pharma gmbh - budesonide - esophageal sykdommer - antidiarrheals, intestinal betennelsesdempende / antiinfective agents - jorveza er indisert for behandling av eosinofiløsofagitt (eoe) hos voksne (eldre enn 18 år).

Namuscla 유럽 연합 - 노르웨이어 - EMA (European Medicines Agency)

namuscla

lupin europe gmbh - mexiletine hydrochloride - myotonic lidelser - hjertetapi - namuscla er indikert for symptomatisk behandling av myotonia hos voksne pasienter med ikke-dystrophic myotonic lidelser.

Giapreza 유럽 연합 - 노르웨이어 - EMA (European Medicines Agency)

giapreza

paion deutschland gmbh - angiotensin ii-acetat - hypotension; shock - agenter som virker på renin-angiotensinsystemet - giapreza er angitt for behandling av refraktær hypotensjon hos voksne med septisk eller andre distributive sjokk som fortsatt hypotensive til tross for tilstrekkelig volum restitusjon og bruk av katekolaminer og andre tilgjengelige vasopressor terapi.

Berinert 3000 IU 노르웨이 - 노르웨이어 - Statens legemiddelverk

berinert 3000 iu

csl behring gmbh (2) - c1-esteraseinhibitor, human - pulver og væske til injeksjonsvæske, oppløsning - 3000 iu

Berinert 2000 IU 노르웨이 - 노르웨이어 - Statens legemiddelverk

berinert 2000 iu

csl behring gmbh (2) - c1-esteraseinhibitor, human - pulver og væske til injeksjonsvæske, oppløsning - 2000 iu

Comirnaty 유럽 연합 - 노르웨이어 - EMA (European Medicines Agency)

comirnaty

biontech manufacturing gmbh - single-stranded, 5’-capped messenger rna 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 - vaksiner - comirnaty 30 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty original/omicron ba. 1 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older who have previously received at least a primary vaccination course against covid-19. comirnaty original/omicron ba. 4-5 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty original/omicron ba. 4-5 (1. 5/1. 5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty omicron xbb. 5 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty omicron xbb. 5 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 10 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years. bruk av denne vaksinen skal være i samsvar med offisielle anbefalinger.

Sugammadex Fresenius Kabi 유럽 연합 - 노르웨이어 - EMA (European Medicines Agency)

sugammadex fresenius kabi

fresenius kabi deutschland gmbh - sugammadex sodium - neuromuskulær blokkade - alle andre terapeutiske produkter - reversal of neuromuscular blockade induced by rocuronium or vecuronium in adults. for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.

Sugammadex Amomed 유럽 연합 - 노르웨이어 - EMA (European Medicines Agency)

sugammadex amomed

aop orphan pharmaceuticals gmbh - sugammadex sodium - neuromuskulær blokkade - alle andre terapeutiske produkter - reversering av nevromuskulær blokade indusert av rocuronium eller vecuronium. for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.