Enteroporc Coli AC Europäische Union - Deutsch - 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 - schweine - 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.

Suiseng Diff/A Europäische Union - Deutsch - EMA (European Medicines Agency)

suiseng diff/a

laboratorios hipra, s.a. - clostridioides difficile toxoid a, clostridioides difficile toxoid b, clostridium perfringens, type a, alpha toxoid - immunologicals for suidae, inactivated bacterial vaccines for pigs, clostridium - schweine - for the passive immunisation of neonatal piglets by means of the active immunisation of breeding sows and gilts:- to prevent mortality and reduce clinical signs and macroscopic lesions caused by clostridioides difficile toxins a and b. - to reduce clinical signs and macroscopic lesions caused by clostridium perfringens type a, alpha toxin.

Purevax RCP Europäische Union - Deutsch - EMA (European Medicines Agency)

purevax rcp

boehringer ingelheim vetmedica gmbh - attenuated feline panleucopenia virus (pli iv) - immunologischen arzneimitteln für felidae, - katzen - active immunisation of cats aged eight 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. onset of immunity is one week after primary vaccination course the duration of immunity is one year after the primary vaccination course and three years after the last re-vaccination.

PreHevbri Europäische Union - Deutsch - EMA (European Medicines Agency)

prehevbri

vbi vaccines b.v. - hepatitis-b-oberflächenantigen - hepatitis b - impfstoffe - prehevbri is indicated for active immunisation against infection caused by all known subtypes of the hepatitis b virus in adults. it can be expected that hepatitis d will also be prevented by immunisation with prehevbri as hepatitis d (caused by the delta agent) does not occur in the absence of hepatitis b infection. the use of prehevbri should be in accordance with official recommendations.

Purevax RC Europäische Union - Deutsch - EMA (European Medicines Agency)

purevax rc

boehringer ingelheim vetmedica gmbh - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains) - immunologischen arzneimitteln für felidae, - katzen - active immunisation of cats aged eight weeks and older:against feline viral rhinotracheitis to reduce clinical signs;against calicivirus infection to reduce clinical signs. onsets of immunity isone week after primary vaccination course. the duration of immunity is one year after primary vaccination course and three years after the last re-vaccination.

Increxxa Europäische Union - Deutsch - EMA (European Medicines Agency)

increxxa

elanco gmbh - tulathromycin - antibiotika zur systemischen anwendung - cattle; pigs; sheep - cattle: treatment and metaphylaxis of bovine respiratory disease (brd) associated with mannheimia haemolytica, pasteurella multocida, histophilus somni and mycoplasma bovis susceptible to tulathromycin. das vorhandensein der krankheit in der herde sollte vor einer metaphylaktischen behandlung festgestellt werden. treatment of infectious bovine keratoconjunctivitis (ibk) associated with moraxella bovis susceptible to tulathromycin. pigs: treatment and metaphylaxis of swine respiratory disease (srd) associated with actinobacillus pleuropneumoniae, pasteurella multocida, mycoplasma hyopneumoniae, haemophilus parasuis and bordetella bronchiseptica susceptible to tulathromycin. das vorhandensein der krankheit in der herde sollte vor einer metaphylaktischen behandlung festgestellt werden. the product should only be used if pigs are expected to develop the disease within 2–3 days. schaf: behandlung der frühen stadien der infektiösen pododermatitis (fußfäule) in verbindung mit dem virulenten dichelobacter nodosus, der eine systemische behandlung erfordert.

Nuvaxovid Europäische Union - Deutsch - EMA (European Medicines Agency)

nuvaxovid

novavax cz, a.s. - sars cov-2 (original) recombinant spike protein, sars-cov-2 (omicron xbb.1.5) recombinant spike protein - covid-19 virus infection - covid-19 vaccines - nuvaxovid is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 12 years of age and older. der einsatz dieses impfstoffs sollte in übereinstimmung mit den offiziellen empfehlungen. nuvaxovid xbb. 5 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 12 years of age and older. der einsatz dieses impfstoffs sollte in übereinstimmung mit den offiziellen empfehlungen.

Tulaven Europäische Union - Deutsch - EMA (European Medicines Agency)

tulaven

ceva santé animale - tulathromycin - antibiotika zur systemischen anwendung - cattle; pigs; sheep - cattle: treatment and metaphylaxis of bovine respiratory disease (brd) associated with mannheimia haemolytica, pasteurella multocida, histophilus somni and mycoplasma bovis susceptible to tulathromycin. das vorhandensein der krankheit in der herde sollte vor einer metaphylaktischen behandlung festgestellt werden. treatment of infectious bovine keratoconjunctivitis (ibk) associated with moraxella bovis susceptible to tulathromycin. pigs: treatment and metaphylaxis of swine respiratory disease (srd) associated with actinobacillus pleuropneumoniae, pasteurella multocida, mycoplasma hyopneumoniae, haemophilus parasuis and bordetella bronchiseptica susceptible to tulathromycin. das vorhandensein der krankheit in der herde sollte vor einer metaphylaktischen behandlung festgestellt werden. the product should only be used if pigs are expected to develop the disease within 2–3 days. schaf: behandlung der frühen stadien der infektiösen pododermatitis (fußfäule) in verbindung mit dem virulenten dichelobacter nodosus, der eine systemische behandlung erfordert.

Lydaxx Europäische Union - Deutsch - EMA (European Medicines Agency)

lydaxx

vetoquinol - tulathromycin - antibiotika zur systemischen anwendung - cattle; pigs; sheep - cattle: treatment and metaphylaxis of bovine respiratory disease (brd) associated with mannheimia haemolytica, pasteurella multocida, histophilus somni and mycoplasma bovis susceptible to tulathromycin. das vorhandensein der krankheit in der herde sollte vor einer metaphylaktischen behandlung festgestellt werden. treatment of infectious bovine keratoconjunctivitis (ibk) associated with moraxella bovis susceptible to tulathromycin. pigs: treatment and metaphylaxis of swine respiratory disease (srd) associated with actinobacillus pleuropneumoniae, pasteurella multocida, mycoplasma hyopneumoniae, haemophilus parasuis and bordetella bronchiseptica susceptible to tulathromycin. das vorhandensein der krankheit in der herde sollte vor einer metaphylaktischen behandlung festgestellt werden. the product should only be used if pigs are expected to develop the disease within 2–3 days. schaf: behandlung der frühen stadien der infektiösen pododermatitis (fußfäule) in verbindung mit dem virulenten dichelobacter nodosus, der eine systemische behandlung erfordert.

Rexxolide Europäische Union - Deutsch - EMA (European Medicines Agency)

rexxolide

dechra regulatory b.v. - tulathromycin - antibiotika zur systemischen anwendung - cattle; pigs; sheep - cattle: treatment and metaphylaxis of bovine respiratory disease (brd) associated with mannheimia haemolytica, pasteurella multocida, histophilus somni and mycoplasma bovis susceptible to tulathromycin. das vorhandensein der krankheit in der herde sollte vor einer metaphylaktischen behandlung festgestellt werden. treatment of infectious bovine keratoconjunctivitis (ibk) associated with moraxella bovis susceptible to tulathromycin. pigs: treatment and metaphylaxis of swine respiratory disease (srd) associated with actinobacillus pleuropneumoniae, pasteurella multocida, mycoplasma hyopneumoniae, haemophilus parasuis and bordetella bronchiseptica susceptible to tulathromycin. das vorhandensein der krankheit in der herde sollte vor einer metaphylaktischen behandlung festgestellt werden. the product should only be used if pigs are expected to develop the disease within 2–3 days. schaf: behandlung der frühen stadien der infektiösen pododermatitis (fußfäule) in verbindung mit dem virulenten dichelobacter nodosus, der eine systemische behandlung erfordert.