Comirnaty Europeiska unionen - svenska - 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 - 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.

Oxbryta Europeiska unionen - svenska - EMA (European Medicines Agency)

oxbryta

pfizer europe ma eeig  - voxelotor - anemia; anemia, hemolytic; anemia, sickle cell - other hematological agents - oxbryta is indicated for the treatment of haemolytic anaemia due to sickle cell disease (scd) in adults and paediatric patients 12 years of age and older as monotherapy or in combination with hydroxycarbamide.

ReoPro 2 mg/ml Injektions-/infusionsvätska, lösning Sverige - svenska - Läkemedelsverket (Medical Products Agency)

reopro 2 mg/ml injektions-/infusionsvätska, lösning

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

Reopro 2 mg/ml Injektions-/infusionsvätska, lösning Sverige - svenska - Läkemedelsverket (Medical Products Agency)

reopro 2 mg/ml injektions-/infusionsvätska, lösning

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

Reopro 2 mg/ml Injektions-/infusionsvätska, lösning Sverige - svenska - Läkemedelsverket (Medical Products Agency)

reopro 2 mg/ml injektions-/infusionsvätska, lösning

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

Reopro 2 mg/ml Injektions-/infusionsvätska, lösning Sverige - svenska - Läkemedelsverket (Medical Products Agency)

reopro 2 mg/ml injektions-/infusionsvätska, lösning

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

Reopro 2 mg/ml Injektions-/infusionsvätska, lösning Sverige - svenska - Läkemedelsverket (Medical Products Agency)

reopro 2 mg/ml injektions-/infusionsvätska, lösning

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

ReoPro 2 mg/ml Injektions-/infusionsvätska, lösning Sverige - svenska - Läkemedelsverket (Medical Products Agency)

reopro 2 mg/ml injektions-/infusionsvätska, lösning

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

Grazax 75 000 SQ-T Frystorkad sublingual tablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

grazax 75 000 sq-t frystorkad sublingual tablett

alk-abelló a/s - allergen, timotejpollen - frystorkad sublingual tablett - 75 000 sq-t - allergen, timotejpollen 75000 sq-t aktiv substans; mannitol hjälpämne - gräspollen

Grazax 75 000 SQ-T Frystorkad tablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

grazax 75 000 sq-t frystorkad tablett

medartuum ab - allergen, timotejpollen - frystorkad tablett - 75 000 sq-t - mannitol hjälpämne; allergen, timotejpollen 75000 sq-t aktiv substans - gräspollen