Den Europæiske Union - dansk - EMA (European Medicines Agency)

valneva austria gmbh - japanese-encephalitis virus, inaktiveret (svækket stamme sa14-14-2 dyrket i vero celler) - encephalitis, japanese; immunization - vacciner - ixiaro er indiceret til aktiv immunisering mod japansk encephalitis hos voksne, unge, børn og spædbørn i alderen to måneder og ældre. ixiaro bør overvejes til brug hos personer i risiko for eksponering gennem rejser eller i forbindelse med udøvelsen af deres erhverv.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

roche registration gmbh - ocrelizumab - multipel sclerose - immunosuppressiva - behandling af voksne patienter med recidiverende former for multipel sklerose (rms) med aktiv sygdom defineret ved kliniske eller billeddannende egenskaber. behandling af voksne patienter med tidlig primær progressiv multipel sklerose (ppm) i form af sygdommens varighed og grad af handicap, og med billedbehandling funktioner karakteristisk for inflammatorisk aktivitet.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

laboratorios hipra, s.a. - mycoplasma hyopneumoniae, strain 7304 (nexhyon), expressing the capsid protein of porcine circovirus type 2a, inactivated - immunologicals for suidae, inactivated viral and inactivated bacterial vaccines - svin - for the active immunisation of pigs:to reduce lung lesions associated with porcine enzootic pneumonia caused by mycoplasma hyopneumoniae. also, to reduce the incidence of these lesions (as observed in field studies). to reduce viraemia, virus load in lungs and lymphoid tissues and the duration of the viraemic period associated with diseases caused by porcine circovirus type 2 (pcv2). efficacy against pcv2 genotypes a, b and d has been demonstrated in field studies. to reduce culling rate and the loss of daily weight gain caused by mycoplasma hyopneumoniae and/or pcv2 related diseases (as observed at 6 months of age in field studies). mycoplasma hyopneumoniae: onset of immunity: 3 weeks after vaccinationduration of immunity: 23 weeks after vaccinationporcine circovirus type 2:onset of immunity: 2 weeks after vaccinationduration of immunity: 22 weeks after vaccinationin addition, a reduction in nasal and faecal shedding and the duration of nasal excretion of pcv2 was demonstrated in animals challenged at 4 weeks and at 22 weeks after vaccination.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

intervet international b.v. - porcint circovirus type 2 (pcv2) orf2 subunit-antigen, mycoplasma hyopneumoniae j stamme inaktiverede - immunologicals for suidae, inactivated viral and inactivated bacterial vaccines - svin (slagtekyllinger) - til aktiv immunisering af svin for at reducere viraemia, virus belastning i lungerne og lymfoide væv, virus kaste forårsaget af porcint circovirus type 2 (pcv2) infektion, og sværhedsgraden af lunge læsioner forårsaget af mycoplasma hyopneumoniae infektion. for at reducere tabet af daglig vægtforøgelse i efterbehandlingstiden i lyset af infektioner med mycoplasma hyopneumoniae og / eller pcv2 (som observeret i feltundersøgelser).

Den Europæiske Union - dansk - EMA (European Medicines Agency)

zoetis belgium sa - inactivated recombinant chimeric porcine circovirus type 1 containing the porcine circovirus type 2 orf2 protein, inactivated mycoplasma hyopneumoniae, strain p-5722-3 - inaktiveret virus og bakterier inaktiverede vacciner - svin - til aktiv immunisering af svin fra 3 ugers alderen mod porcine circovirus type 2 (pcv2) for at reducere viral belastning i blod og lymfoide væv og fækalt afgivelse forårsaget af infektion med pcv2. til aktiv immunisering af svin over 3 uger mod mycoplasma hyopneumoniae for at reducere lungelæsioner forårsaget af infektion med m. hyopneumoniae.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

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 - immunologiske stoffer til suidae - svin (slagtekyllinger) - 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.

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

elanco gmbh - mycoplasma hyopneumoniae, stamme p-5722-3 (inaktiveret) - injektionsvæske, emulsion - 6000 ru/dosis - svin

Den Europæiske Union - dansk - EMA (European Medicines Agency)

resilience biomanufacturing ireland limited - influenzavaccine (hel virion, inaktiveret) indeholdende antigen af: a / vietnam / 1203/2004 (h5n1) - influenza, human; immunization; disease outbreaks - vacciner - prophylax af influenza i en officielt erklæret pandemisk situation. pandemic influenza vaccine bør anvendes i overensstemmelse med officielle retningslinjer.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

novartis vaccines and diagnostics s.r.l. - influenzavirusoverfladeantigener (hæmagglutinin og neuraminidase) af stamme a / viet nam / 1194/2004 (h5n1) - influenza, human; immunization; disease outbreaks - vacciner - aktiv immunisering mod h5n1-subtype af influenza 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.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

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.