Porcilis ColiClos Unia Europejska - polski - EMA (European Medicines Agency)

porcilis coliclos

intervet international bv - laseczka filtrów typu c / e. coli f4ab / f4ac e. coli / e. coli Ф5 / f6. e. coli / e. coli lt - immunologiczne - wieprzowy - dla pasywnej immunizacji potomstwa poprzez aktywną szczepień loch i подсвинков w celu zmniejszenia śmiertelności i objawów klinicznych w ciągu pierwszych dni życia, spowodowane jest tym, szczepy escherichia coli, które wyrażają адгезинов f4ab (k88ab), f4ac (k88ac), Ф5 (k99) lub f6 (987p) i spowodowane przez clostridium filtrów typu c.

Porcilis Porcoli Diluvac Forte (previously Porcilis Porcoli) Unia Europejska - polski - EMA (European Medicines Agency)

porcilis porcoli diluvac forte (previously porcilis porcoli)

intervet international bv - f4ab (k88ab) fimbrial адгезиного, f4ac (k88ac) fimbrial адгезиного, Ф5 (k99) fimbrial адгезиного, f6. (987p) fimbrial адгезиного, lt anatoksinu - immunologiczne - Świnie (loszki i maciory) - dla pasywnej immunizacji prosiąt aktywnej szczepień loch / remontowych świnek w celu zmniejszenia śmiertelności i objawów klinicznych, takich jak biegunka z powodu enterotoxicosis noworodków w pierwszych dniach życia, spowodowane tym, e. szczepy coli eksprymujące adhezyny fimbrialne f4ab (k88ab), f4ac (k88ac), f5 (k99) lub f6 (987p).

Enteroporc Coli AC Unia Europejska - polski - EMA (European Medicines Agency)

enteroporc coli ac

ceva santé animale - clostridium perfringens type c, beta1 toxoid / clostridium perfringens, type a, alpha toxoid / clostridium perfringens, type a, beta2 toxoid / escherichia coli, fimbrial adhesin f4ab / escherichia coli, fimbrial adhesin f4ac / escherichia coli, fimbrial adhesin f5 / escherichia coli, fimbrial adhesin f6 - immunologicals for suidae, inactivated bacterial vaccines (including mycoplasma, toxoid and chlamydia) escherichia + clostridium - wieprzowy - for the passive immunisation of progeny by active immunisation of pregnant sows and gilts to reduce:-           clinical signs (severe diarrhoea) and mortality caused by escherichia coli strains expressing the fimbrial adhesins f4ab, f4ac, f5 and f6-           clinical signs (diarrhoea during the first days of life) associated with clostridium perfringens type a expressing alpha and beta 2 toxins-           clinical signs and mortality associated with haemorrhagic and necrotising enteritis caused by clostridium perfringens type c expressing beta1 toxin.

Enteroporc Coli Unia Europejska - polski - EMA (European Medicines Agency)

enteroporc coli

ceva santé animale - inactivated fimbrial adhesins of escherichia coli f4ab, inactivated fimbrial adhesins of escherichia coli f4ac, inactivated fimbrial adhesins of escherichia coli f5, inactivated fimbrial adhesins of escherichia coli f6 - immunologiczne dla suidae - wieprzowy - for the passive immunisation of progeny by active immunisation of pregnant sows and gilts to reduce clinical signs (severe diarrhoea) and mortality caused by escherichia coli strains expressing the fimbrial adhesins f4ab, f4ac, f5 and f6.

Prepandemic influenza vaccine (H5N1) (surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics Unia Europejska - polski - EMA (European Medicines Agency)

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

novartis vaccines and diagnostics s.r.l. - antygeny powierzchniowe wirusa grypy (hemaglutynina i neuraminidaza) szczepu a / viet nam / 1194/2004 (h5n1) - influenza, human; immunization; disease outbreaks - szczepionki - aktywna immunizacja przeciwko podtypowi h5n1 wirusa grypy a.. , , 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 Unia Europejska - polski - EMA (European Medicines Agency)

covid-19 vaccine (inactivated, adjuvanted) valneva

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

Zoonotic Influenza Vaccine Seqirus Unia Europejska - polski - EMA (European Medicines Agency)

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 - szczepionki - active immunisation against h5 subtype of influenza a virus.

Mhyosphere PCV ID Unia Europejska - polski - EMA (European Medicines Agency)

mhyosphere pcv id

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 - wieprzowy - 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.

Pandemic influenza vaccine H5N1 AstraZeneca (previously Pandemic influenza vaccine H5N1 Medimmune) Unia Europejska - polski - EMA (European Medicines Agency)

pandemic influenza vaccine h5n1 astrazeneca (previously pandemic influenza vaccine h5n1 medimmune)

astrazeneca ab - reasortant wirusa grypy (żywego atenuowanego) następującego szczepu: a / vietnam / 1203/2004 (h5n1) - grypa, człowiek - szczepionki - profilaktyka grypy w oficjalnie ogłoszonej pandemii u dzieci i młodzieży w wieku od 12 miesięcy do poniżej 18 lat. szczepionki przeciwko pandemii grypy h5n1 АстраЗенека powinny być stosowane zgodnie z oficjalnym kierunkiem.