Quintanrix Europese Unie - Slowaaks - EMA (European Medicines Agency)

quintanrix

glaxosmithkline biologicals s.a. - preventívne očkovanie proti záškrtu toxoid, tetanus toxoid, inaktivované bordetella pertussis, hepatitída b povrchových antigénov (rdna), hemofilovm influenzae typ b polysacharid - hepatitis b; tetanus; immunization; meningitis, haemophilus; whooping cough; diphtheria - vakcíny - quintanrix je indikovaný na primárnu imunizáciu dojčiat (počas prvého roka života) proti diftérii, tetanu, čiernemu kašľu, hepatitíde b, invazívnych ochorení spôsobených haemophilus influenzae typu b a posilňovacej imunizácii malých detí počas druhom roku života. použitie quintanrix by mali byť stanovené na základe oficiálnych odporúčaní.

Evusheld Europese Unie - Slowaaks - EMA (European Medicines Agency)

evusheld

astrazeneca ab - tixagevimab, cilgavimab - covid-19 virus infection - prevention of covid-19.

Azibiot NEO 40 mg/ml prášok na perorálnu suspenziu Slowakije - Slowaaks - ŠÚKL (Štátny ústav pre kontrolu liečiv)

azibiot neo 40 mg/ml prášok na perorálnu suspenziu

krka, d.d., novo mesto, slovinsko - azitromycín - 15 - antibiotica (proti mikrob. a vÍrusovÝm infekciam)

Azibiot NEO 20 mg/ml prášok na perorálnu suspenziu Slowakije - Slowaaks - ŠÚKL (Štátny ústav pre kontrolu liečiv)

azibiot neo 20 mg/ml prášok na perorálnu suspenziu

krka, d.d., novo mesto, slovinsko - azitromycín - 15 - antibiotica (proti mikrob. a vÍrusovÝm infekciam)

Prevexxion RN+HVT+IBD Europese Unie - Slowaaks - EMA (European Medicines Agency)

prevexxion rn+hvt+ibd

boehringer ingelheim vetmedica gmbh - live recombinant marek’s disease virus, serotype 1, strain rn1250; live recombinant turkey herpesvirus, expressing the vp2 protein of infectious bursal disease virus, strain vhvt013-69 - immunologicals for aves, domestic fowl, avian herpes virus (marek's disease) + avian infectious bursal disease virus (gumboro disease) + newcastle disease virus/paramyxovirus - kura - for active immunisation of one-day-old chicks to prevent mortality and clinical signs and reduce lesions caused by marek’s disease (md) virus (including very virulent md virus), and to prevent mortality, clinical signs and lesions caused by infectious bursal disease (ibd) virus.

Ticagrelor Swyssi 90 mg Slowakije - Slowaaks - ŠÚKL (Štátny ústav pre kontrolu liečiv)

ticagrelor swyssi 90 mg

swyssi ag, nemecko - tikagrelor - 16 - anticoagulantia (fibrinolytica, antifibrinol.)

Ticagrelor Swyssi 60 mg Slowakije - Slowaaks - ŠÚKL (Štátny ústav pre kontrolu liečiv)

ticagrelor swyssi 60 mg

swyssi ag, nemecko - tikagrelor - 16 - anticoagulantia (fibrinolytica, antifibrinol.)

Purevax RCP FeLV Europese Unie - Slowaaks - EMA (European Medicines Agency)

purevax rcp felv

boehringer ingelheim vetmedica gmbh - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains), attenuated feline panleucopenia virus (pli iv), felv recombinant canarypox virus (vcp97) - immunologicals pre felidae, - mačky - active immunisation of cats aged 8 weeks and older:against feline viral rhinotracheitis to reduce clinical signs;against calicivirus infection to reduce clinical signs ;against feline panleucopenia to prevent mortality and clinical signs;against leukaemia to prevent persistent viraemia and clinical signs of the related disease. onsets of immunity are 1 week after primary vaccination course for rhinotracheitis, calicivirus and panleucopenia components, and 2 weeks after primary vaccination course for feline leukaemia component. the duration of immunity is one year after the last re-vaccination for the feline leukaemia component, and one year after primary vaccination course and three years after the last re-vaccination for the rhinotracheitis, calicivirosis and panleucopenia components.

Purevax RCPCh FeLV Europese Unie - Slowaaks - EMA (European Medicines Agency)

purevax rcpch felv

boehringer ingelheim vetmedica gmbh - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains), attenuated feline panleucopenia virus (pli iv), felv recombinant canarypox virus (vcp97), attenuated chlamydophila felis (905 strain) - immunologicals pre felidae, - mačky - active immunisation of cats aged 8 weeks and older:against feline viral rhinotracheitis to reduce clinical signs;against calicivirus infection to reduce clinical signs;against chlamydophila felis infection to reduce clinical signs;against feline panleucopenia to prevent mortality and clinical signs;against leukaemia to prevent persistent viraemia and clinical signs of the related disease. onsets of immunity are 1 week after primary vaccination course for rhinotracheitis, calicivirus, chlamydophila felis and panleucopenia components, and 2 weeks after primary vaccination course for feline leukaemia component. the duration of immunity is one year after the last re-vaccination for the chlamydiosis and feline leukaemia components, and one year after primary vaccination course and three years after the last re-vaccination for the rhinotracheitis, calicivirosis and panleucopenia components.

Nobivac DP Plus Europese Unie - Slowaaks - EMA (European Medicines Agency)

nobivac dp plus

intervet international b.v. - live attenuated canine distemper virus strain onderstepoort: 105.1 – 106.5 tcid50, live recombinant canine parvovirus strain 630a: 105.1 – 106.7 tcid50 - imunologické vyšetrenie pre kanáriky - dogs (small) - for the active immunisation of puppies from 4 weeks of age onwards to prevent clinical signs and mortality of canine distemper virus infection and canine parvovirus infection and to prevent viral excretion following canine distemper virus infection and following canine parvovirus infection.