prepandemic influenza vaccine (h5n1) (surface antigen, inactivated, adjuvanted) novartis vaccines and diagnostics
novartis vaccines and diagnostics s.r.l. - influensavirusytantigener (hemagglutinin och neuraminidas) av stam a / viet nam / 1194/2004 (h5n1) - influenza, human; immunization; disease outbreaks - vacciner - aktiv immunisering mot h5n1-subtyp av influensa a-virus. , , this indication is based on immunogenicity data from healthy subjects from the age of 18 years onwards following administration of two doses of the vaccine containing a/vietnam/1194/2004 (h5n1)-like strain. , , prepandemic influenza vaccine (h5n1) novartis vaccines and diagnostic should be used in accordance with official recommendations.
covid-19 vaccine (inactivated, adjuvanted) valneva
valneva austria gmbh - covid-19 vaccine (inactivated, adjuvanted, adsorbed) - covid-19 virus infection - vacciner - covid-19 vaccine (inactivated, adjuvanted) valneva is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 18 to 50 years of age. the use of this vaccine should be in accordance with official recommendations.
pandemic influenza vaccine h5n1 astrazeneca (previously pandemic influenza vaccine h5n1 medimmune)
astrazeneca ab - reassortant influensavirus (levande dämpad) av följande stam: a / vietnam / 1203/2004 (h5n1) stam - influensa, människa - vacciner - profylax av influensa i en officiellt deklarerad pandemisk situation hos barn och ungdomar från 12 månader till yngre än 18 år. pandemic influenza vaccine h5n1 astrazeneca bör användas i enlighet med officiella riktlinjer.
prepandemic influenza vaccine (h5n1) (split virion, inactivated, adjuvanted) glaxosmithkline biologicals
glaxosmithkline biologicals s.a. - delat influensavirus, inaktiverat, innehållande antigen: a / vietnam / 1194/2004 (h5n1) som använt påfrestning (nibrg-14) - influenza, human; immunization; disease outbreaks - vacciner - aktiv immunisering mot h5n1-subtyp av influensa a-virus. denna indikation baseras på immunogenicitet data från friska individer från 18 år och framåt efter administrering av två doser av vaccinet beretts från a/vietnam/1194/2004 nibrg-14 (h5n1) (se avsnitt 5. prepandemic influenza vaccine (h5n1) (split virion, inaktiverat, med adjuvans) glaxosmithkline biologiska 3. 75 µg bör användas i enlighet med officiella riktlinjer.
zoonotic influenza vaccine seqirus
seqirus s.r.l. - zoonotic influenza vaccine (h5n1) (surface antigen, inactivated, adjuvanted), influenza virus surface antigens (haemagglutinin and neuraminidase) of strain: a/turkey/turkey/1/05 (h5n1)-like strain (nibrg-23) - influenza a virus, h5n1 subtype - vacciner - active immunisation against h5 subtype of influenza a virus.
pumarix
glaxosmithkline biologicals s.a. - pandemic influenza vaccine (h5n1) (split virion, inaktiverat, med adjuvans) - influenza, human; immunization; disease outbreaks - vacciner - profylax av influensa i en officiellt deklarerad pandemisk situation. pandemi-influensa-vaccinet bör användas i enlighet med officiella riktlinjer.
pandemic influenza vaccine h5n1 baxter ag
resilience biomanufacturing ireland limited - influensavaccin (helvirion, inaktiverad) innehållande antigen av: a / vietnam / 1203/2004 (h5n1) - influenza, human; immunization; disease outbreaks - vacciner - profylax av influensa i en officiellt deklarerad pandemisk situation. pandemiskt influensavaccin ska användas enligt officiell vägledning.
sandimmun neoral 100 mg/ml oral lösning
paranova läkemedel ab - ciklosporin - oral lösning - 100 mg/ml - makrogolglycerolhydroxistearat hjälpämne; ciklosporin 100 mg aktiv substans; propylenglykol hjälpämne; etanol, vattenfri hjälpämne - ciklosporin
vivotif oralt vaccin mot tyfoid enterokapsel, hård
paxvax ltd - salmonella typhi, stam ty21a, levande försvagad - enterokapsel, hård - salmonella typhi, stam ty21a, levande försvagad 9,3 log10 cfu aktiv substans; sackaros hjälpämne; laktos (vattenfri) hjälpämne - levande försvagat
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.