Europeiska unionen - svenska - EMA (European Medicines Agency)

n.v. organon - desloratadine, pseudophedrine sulfate - rhinit, allergisk, seasonal - nasalberedningar - symtomatisk behandling av säsongsallergisk rinit när den åtföljs av nasal congestion.

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

narodowe centrum badan jadrowych - tetrakis (1 isocyanid-2-metoxi-2-metylpropyl)koppar(i) tetrafluorborat - beredningssats för radioaktivt läkemedel - 1 mg - tetrakis (1 isocyanid-2-metoxi-2-metylpropyl)koppar(i) tetrafluorborat 1 mg aktiv substans; mannitol hjälpämne - teknetium(tc-99m)sestamibi

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

narodowe centrum badan jadrowych - natriummolybdat(mo-99); natriumperteknetat(tc-99m) - radionuklidgenerator - 8 - 175 gbq - natriumperteknetat(tc-99m) 8 - 175 gbq aktiv substans; natriummolybdat(mo-99) 9,1 - 200 gbq aktiv substans - teknetium(tc-99m)perteknetat

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

narodowe centrum badan jadrowych - hynic-(d-phe-1-tyr-3-oktreotid)-trifluoroacetat (1:2) - beredningssats för radioaktivt läkemedel - 20 mikrogram - mannitol hjälpämne; hynic-(d-phe-1-tyr-3-oktreotid)-trifluoroacetat (1:2) 50 mikrog aktiv substans

Europeiska unionen - svenska - EMA (European Medicines Agency)

dynavax gmbh - hepatit b-ytantigen - hepatit b - vacciner - heplisav b is indicated for the active immunisation against hepatitis b virus infection (hbv) caused by all known subtypes of hepatitis b virus in adults 18 years of age and older. the use of heplisav b should be in accordance with official recommendations. it can be expected that hepatitis d will also be prevented by immunisation with heplisav b as hepatitis d (caused by the delta agent) does not occur in the absence of hepatitis b infection.

Europeiska unionen - svenska - EMA (European Medicines Agency)

incline therapeutics europe ltd - fentanylhydroklorid - smärta, postoperativ - smärtstillande medel - ionsys är indicerat för hantering av akut måttlig till svår postoperativ smärta hos vuxna patienter.

Europeiska unionen - svenska - EMA (European Medicines Agency)

janssen-cilag international nv - fentanylhydroklorid - smärta, postoperativ - smärtstillande medel - hantering av akut måttlig till svår postoperativ smärta för användning i en sjukhusinställning.

Europeiska unionen - svenska - EMA (European Medicines Agency)

merck sharp dohme ltd - humant papillomvirus typ 6 l1 protein, humant papillomvirus typ 11 l1 protein, humant papillomvirus typ 16 l1 protein, humant papillomvirus typ 18 l1 protein - papillomavirus infections; uterine cervical dysplasia; condylomata acuminata; immunization - vacciner - silgard är ett vaccin för användning från 9 års ålder år för förebyggande av:premaligna genitala lesioner (cervix, vulva och vagina), premaligna anal lesioner, livmoderhalscancer och anal cancer kausalt relaterade till vissa onkogena humant papillomavirus (hpv) typer, genitala vårtor (kondylom) kausalt relaterade till specifika hpv-typer. se avsnitt 4. 4 och 5. 1 för viktig information om de data som stöder denna indikation. användning av silgard bör ske i enlighet med officiella rekommendationer.

Europeiska unionen - svenska - EMA (European Medicines Agency)

roche registration limited - emicizumab - hemofili a - hemostatika - hemlibra is indicated for routine prophylaxis of bleeding episodes in patients with haemophilia a (congenital factor viii deficiency):with factor viii inhibitorswithout factor viii inhibitors who have:severe disease (fviii < 1%)moderate disease (fviii ≥ 1% and ≤ 5%) with severe bleeding phenotype. hemlibra kan användas i alla åldersgrupper.

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.