COVID-19 Vaccine (inactivated, adjuvanted) Valneva Den europeiske union - norsk - EMA (European Medicines Agency)

covid-19 vaccine (inactivated, adjuvanted) valneva

valneva austria gmbh - covid-19 vaccine (inactivated, adjuvanted, adsorbed) - covid-19 virus infection - vaksiner - 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.

Innovax-ND-IBD Den europeiske union - norsk - EMA (European Medicines Agency)

innovax-nd-ibd

intervet international b.v. - celle-forbundet live rekombinant tyrkia herpes-virus (belastning hvp360), uttrykker fusion protein av nd-virus og vp2 protein av ibd virus - avian herpes virus (marek ' s sykdom) + avian smittsomme bursal disease virus (gumboro sykdom) + newcastle disease virus/paramyxovirus - chicken; embryonated chicken eggs - for active immunisation of one-day-old chicks or 18-19-day-old embryonated chicken eggs:to reduce mortality and clinical signs caused by newcastle disease (nd) virus,to prevent mortality and to reduce clinical signs and lesions caused by infectious bursal disease (ibd) virus,to reduce mortality, clinical signs and lesions caused by marek’s disease (md) virus.

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

abrysvo

pfizer europe ma eeig - respiratory syncytial virus, subgroup a, stabilized prefusion f protein / respiratory syncytial virus, subgroup b, stabilized prefusion f protein - respiratorisk syncytialvirusinfeksjoner - vaksiner - abrysvo is indicated for:passive protection against lower respiratory tract disease caused by respiratory syncytial virus (rsv) in infants from birth through 6 months of age following maternal immunisation during pregnancy. se avsnitt 4. 2 og 5. active immunisation of individuals 60 years of age and older for the prevention of lower respiratory tract disease caused by rsv. bruk av denne vaksinen skal være i samsvar med offisielle anbefalinger.

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

circomax myco

zoetis belgium - inactivated mycoplasma hyopneumoniae, strain p-5722-3, inactivated recombinant chimeric porcine circovirus type 1 containing the porcine circovirus type 2a open reading frame 2 (orf2) protein, inactivated recombinant chimeric porcine circovirus type 1 containing the porcine circovirus type 2b orf2 protein - immunologicals for suidae - griser (for fetende) - active immunisation of pigs against porcine circovirus type 2 to reduce viral load in blood and lymphoid tissues, fecal shedding and the lesions in lymphoid tissues associated with pcv2 infection. protection was demonstrated against porcine circovirus types 2a, 2b and 2d. active immunisation of pigs against mycoplasma hyopneumoniae to reduce the lung lesions associated with mycoplasma hyopneumoniae infection.  onset of immunity (both vaccination schedules): 3 weeks after (the last) vaccination.  duration of immunity (both vaccination schedules): 23 weeks after (the last) vaccination.  in addition, vaccination has been shown to reduce body weight gain losses under field conditions.

Innovax-ND-ILT Den europeiske union - norsk - EMA (European Medicines Agency)

innovax-nd-ilt

intervet international b.v. - cell-associated live recombinant turkey herpesvirus (strain hvt/ndv/ilt) expressing the fusion protein of newcastle disease virus and the glycoproteins gd and gi of infectious laryngotracheitis virus - immunologicals for aves - embryonated chicken eggs; chicken - for active immunisation of one-day-old chicks or embryonated chicken eggs:to reduce mortality and clinical signs caused by newcastle disease (nd) virus,to reduce mortality, clinical signs and lesions caused by avian infectious laryngotracheitis (ilt) virus and marek’s disease (md) virus.

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

zulvac btv

zoetis belgium sa - ett av følgende inaktivert bluetongue virusartene:inaktivert bluetongue virus, serotype 1, belastning btv-1/alg2006/01 e1inactivated bluetongue virus, serotype 8, belastning btv-8/bel2006/02inactivated bluetongue virus, serotype 4, belastning spa-1/2004 - immunologicals, immunologicals for bovidae, inaktivert viral vaksiner, bluetongue virus, sauer - sheep; cattle - aktiv vaksinering av sau fra 6 ukers alder for forebygging av viraemia forårsaket av bluetongue virus, serotypes 1 og 8, og for reduksjon av viraemia forårsaket av bluetongue virus, serotype 4 og aktiv vaksinering av storfe fra 12 ukers alder for forebygging av viraemia forårsaket av bluetongue virus, serotypes 1 og 8.

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

eravac

laboratorios hipra, s.a. - inactivated rabbit haemorrhagic disease type 2 virus (rhdv2), strainv-1037 - inaktivert viral vaksiner - kaniner - for aktive vaksinering av kaniner fra en alder av 30 dager for å redusere dødelighet forårsaket av kanin blødningssykdom type 2-viruset (rhdv2).

Prepandemic influenza vaccine (H5N1) (surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics Den europeiske union - norsk - EMA (European Medicines Agency)

prepandemic influenza vaccine (h5n1) (surface antigen, inactivated, adjuvanted) novartis vaccines and diagnostics

novartis vaccines and diagnostics s.r.l. - influensavirusoverflateantigener (hemagglutinin og neuraminidase) av stamme a / viet nam / 1194/2004 (h5n1) - influenza, human; immunization; disease outbreaks - vaksiner - aktiv immunisering mot h5n1 subtype 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.

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

celvapan

nanotherapeutics bohumil, s.r.o. - whole virion influenza vaccine, inactivated containing antigen of strain a/california/07/2009 (h1n1)v - disease outbreaks; influenza, human; immunization - vaksiner - profylakse av influensa forårsaket av a (h1n1) v 2009 virus. celvapan bør brukes i samsvar med offisielle veiledning.

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

eryseng parvo

laboratorios hipra, s.a. - porcine parvovirus, stamme nadl-2 og erysipelothrix rhusiopathiae, stamme r32e11 (inaktivert) - immunologicals for suidae, inactivated viral and inactivated bacterial vaccines - griser - for aktiv immunisering av kvinnelige griser for beskyttelse av avkom mot transplacental infeksjon forårsaket av svin parvovirus. for aktiv immunisering av hann og svin for å redusere kliniske tegn (hudlesjoner og feber) av svin erysipelas forårsaket av erysipelothrix rhusiopathiae, serotype 1 og serotype 2.