Sverige - svenska - Läkemedelsverket (Medical Products Agency)

prothya biosolutions netherlands b.v - koagulationsfaktor ii, human; koagulationsfaktor ix, human; koagulationsfaktor vii, human; koagulationsfaktor x, human; protein c, humant; protein s, humant - pulver och vätska till injektionsvätska, lösning - 500 ie - koagulationsfaktor ii, human 280 - 700 ie aktiv substans; koagulationsfaktor vii, human 140 - 400 ie aktiv substans; koagulationsfaktor ix, human 500 ie aktiv substans; koagulationsfaktor x, human 280 - 700 ie aktiv substans; protein c, humant 220 - 780 ie aktiv substans; protein s, humant 20 - 160 ie aktiv substans

Europeiska unionen - svenska - EMA (European Medicines Agency)

amryt pharmaceuticals dac - dry extract from birch bark (der 5-10 : 1), extraction solvent n-heptane 95% (w/w) - epidermolysis bullosa dystrophica; epidermolysis bullosa, junctional - förberedelser för behandling av sår och sår - treatment of partial thickness wounds associated with dystrophic and junctional epidermolysis bullosa (eb) in patients 6 months and older.

Europeiska unionen - svenska - EMA (European Medicines Agency)

almirall, s.a. - lebrikizumab - dermatit, atopisk - andra dermatologiska preparat - ebglyss is indicated for the treatment of moderate-to-severe atopic dermatitis in adults and adolescents 12 years and older with a body weight of at least 40 kg who are candidates for systemic therapy.

Europeiska unionen - svenska - EMA (European Medicines Agency)

allergan pharmaceuticals international limited - eluxadoline - irritable bowel syndrome; diarrhea - antidiarrheals, tarm -, antiinflammatoriska / antiinfective agenter - truberzi är indicerat hos vuxna för behandling av irritabelt tarmsyndrom med diarré (ibs d).

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

galderma nordic ab - adapalen; bensoylperoxid, hydratiserad - gel - 0,3 %/2,5 % - bensoylperoxid, hydratiserad 34 mg aktiv substans; glycerol hjälpämne; adapalen 3 mg aktiv substans; propylenglykol hjälpämne

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

orifarm ab - adapalen; bensoylperoxid, hydratiserad - gel - 0,3 %/2,5 % - propylenglykol hjälpämne; adapalen 3 mg aktiv substans; bensoylperoxid, hydratiserad 34 mg aktiv substans; glycerol hjälpämne

Europeiska unionen - svenska - 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 - vacciner - 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. användning av detta vaccin bör ske i enlighet med officiella rekommendationer.

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

janssen biologics b.v. - abciximab - injektions-/infusionsvätska, lösning - 2 mg/ml - abciximab 2 mg aktiv substans - abciximab

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

orifarm ab - abciximab - injektions-/infusionsvätska, lösning - 2 mg/ml - abciximab 2 mg aktiv substans - abciximab

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

orifarm ab - abciximab - injektions-/infusionsvätska, lösning - 2 mg/ml - abciximab 2 mg aktiv substans - abciximab