Den europeiske union - norsk - EMA (European Medicines Agency)

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.

Norge - norsk - Statens legemiddelverk

orifarm as - humant papillomavirus, type 6 l1 protein, rekombinant / humant papillomavirus, type 11 l1 protein, rekombinant / humant papillomavirus, type 16 l1 protein, rekombinant / humant papillomavirus, type 18 l1 protein, rekombinant / humant papillomavirus, type 31 l1 protein, rekombinant / humant papillomavirus, type 33 l1 protein, rekombinant / humant papillomavirus, type 45 l1 protein, rekombinant / humant papillomavirus, type 52 l1 protein, rekombinant / humant papillomavirus, type 58 l1 protein, rekombinant - injeksjonsvæske, suspensjon

Den europeiske union - norsk - EMA (European Medicines Agency)

pharmsure veterinary products europe ltd - mycoplasma synoviae stamme ms-h - immunologicals for aves, live bakteriell vaksiner - kylling - for aktiv immunisering av fremtidige kyllingfôrkyllinger, fremtidige lagfôrkyllinger og fremtidige lagkyllinger for å redusere luftsukleskader og redusere antall egg med unormal skalldannelse forårsaket av mycoplasma synoviae.

Norge - norsk - Statens legemiddelverk

bayer ab - solna - cyproteronacetat - tablett - 50 mg

Norge - norsk - Statens legemiddelverk

orifarm as - cyproteronacetat - tablett - 50 mg

Norge - norsk - Statens legemiddelverk

orifarm as - cyproteronacetat - tablett - 50 mg

Norge - norsk - Statens legemiddelverk

mcneil sweden ab - natriumsitrat / natriumlaurylsulfoacetat / sorbitol - rektalvæske, oppløsning - 90 mg/ ml / 9 mg/ ml / 625 mg/ ml

Den europeiske union - norsk - EMA (European Medicines Agency)

merck europe b.v. - cetrorelix (as acetate) - ovulation; ovulation induction - hypofysiske og hypotalamiske hormoner og analoger - forebygging av tidlig eggløsning hos pasienter som gjennomgår kontrollert ovarie-stimulering, etterfulgt av oocyt-pick-up og assistert reproduksjonsteknikker. i kliniske studier, cetrotide ble brukt i forbindelse med human menopausal gonadotropin (hmg), men begrenset erfaring med rekombinant follicule-stimulerende hormon (fsh) foreslo lignende effekt.

Den europeiske union - norsk - EMA (European Medicines Agency)

laboratoire hra pharma - ulipristal - prevensjon, postcoital - sex hormoner og modulatorer av genital systemet, , nødprevensjon - nødpreventjon innen 120 timer (fem dager) av ubeskyttet samleie eller prevensjonsfeil.

Den europeiske union - norsk - EMA (European Medicines Agency)

bial - portela ca, s.a. - eslikarbazepinacetat - epilepsi - antiepileptics, - exalief er angitt som tilleggsbehandling behandling hos voksne med delvis-utbruddet anfall med eller uten sekundær generalisering.