Euroopan unioni - malta - EMA (European Medicines Agency)

zoetis belgium sa - live recombinant e2 gene-deleted bovine viral diarrhoea virus containing classical swine fever virus e2 gene (cp7_e2alf) - live viral vaccines, immunologicals for suidae - majjali - għal immunizzazzjoni attiva ta 'majjali minn 7 ġimgħat' il quddiem biex tevita l-mortalità u tnaqqas l-infezzjoni u l-mard ikkawżat mill-virus tad-deni klassiku tal-ħnieżer (csfv). onset of immunity: 14 days after vaccinationduration of immunity: at least 6 months after vaccinationfor active immunisation of breeding females to reduce transplacental infection caused by csfv. onset of immunity: 21 days after vaccinationduration of immunity has not been demonstrated.

Euroopan unioni - malta - EMA (European Medicines Agency)

zoetis belgium sa - virus rikombinanti taċ-circovirus porċin (cpcv) 1-2, inattivat - immunoloġiċi - majjali (ħnienes) - immunizzazzjoni attiva ta 'qżieqeż fuq l-età ta' tliet ġimgħat kontra l-virus porcine circovirus tip 2 (pcv2) biex titnaqqas it-tagħbija virali fid-demm u fit-tessuti limfodje, u l-leżjonijiet f'tessuti limfojde assoċjati ma 'infezzjoni b'pcv2, kif ukoll biex tnaqqas sinjali kliniċi - li jinkludu telf ta 'kuljum ta' żieda fil-piż, u l-mortalità assoċjata ma wara l-ftim tal-ġisem, ħela sindromu.

Euroopan unioni - malta - EMA (European Medicines Agency)

zoetis belgium sa - klieb distemper virus, razza cdv bio 11/a, klieb adenovirus tat-tip 2, razza cav-2 bio 13, klieb parvovirus tip 2b, razza cpv-2b bio 12/b u l-klieb parainfluenza tat-tip 2 virus, razza cpiv-2 bio 15 (kollha ħaj attenwat) - immunoloġiċi għall-canidae, vaċċini virali Ħajjin - klieb - immunizzazzjoni attiva ta 'klieb minn sitt ġimgħat. biex tipprevjeni l-mortalità u sinjali kliniċi ikkawżati mill-klieb distemper virus,biex jimpedixxi l-mortalità u sinjali kliniċi ikkawżati mill-klieb adenovirus tat-tip 1,li jipprevjenu l-sinjali kliniċi u l-eskrezzjoni virali kkawżata mill-klieb adenovirus tat-tip 2,għall-prevenzjoni ta ' sinjali kliniċi, lewkopenija u l-eskrezzjoni virali kkawżata mill-klieb parvovirus,għall-prevenzjoni tal-sinjali kliniċi u l-eskrezzjoni virali kkawżata mill-klieb parainfluenza virus.

Euroopan unioni - malta - EMA (European Medicines Agency)

virbac s.a. - halofuginone - antiprotozoali - għoġġiela, twelid - in new born calves:- prevention of diarrhoea due to diagnosed cryptosporidium parvum, in farms with history of cryptosporidiosis,administration should start in the first 24 to 48 hours of age- reduction of diarrhoea due to diagnosed cryptosporidium parvum. l-amministrazzjoni għandha tibda fi żmien 24 siegħa wara l-bidu tad-dijarea. fiż-żewġ każijiet, it-tnaqqis ta 'l-eliminazzjoni ta' l-ooċisti intwera.

Euroopan unioni - malta - EMA (European Medicines Agency)

virbac s.a. - tulathromycin - antibacterials għal użu sistemiku - 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. il-preżenza tal-marda fil-merħla għandha tiġi stabbilita qabel it-trattament metaphylactic. 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. il-preżenza tal-marda fil-merħla għandha tiġi stabbilita qabel it-trattament metaphylactic. the product should only be used if pigs are expected to develop the disease within 2–3 days. nagħaġ: trattament tal-istadji bikrija ta 'pododermatite infettiva (taħsir tas-sieq) assoċjat ma' dichelobacter nodosus virulenti li jeħtieġ trattament sistemiku.

Euroopan unioni - malta - EMA (European Medicines Agency)

ceva santé animale - tulathromycin - antibacterials għal użu sistemiku - 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. il-preżenza tal-marda fil-merħla għandha tiġi stabbilita qabel it-trattament metaphylactic. 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. il-preżenza tal-marda fil-merħla għandha tiġi stabbilita qabel it-trattament metaphylactic. the product should only be used if pigs are expected to develop the disease within 2–3 days. nagħaġ: trattament tal-istadji bikrija ta 'pododermatite infettiva (taħsir tas-sieq) assoċjat ma' dichelobacter nodosus virulenti li jeħtieġ trattament sistemiku.

Euroopan unioni - malta - EMA (European Medicines Agency)

elanco gmbh - lotilaner, milbemycin oxime - endectoċidi - klieb - for use in dogs with, or at risk from, mixed infestations/infections of ticks, fleas, gastrointestinal nematodes, heartworm and/or lungworm.

Euroopan unioni - malta - EMA (European Medicines Agency)

orion corporation - pregabalin - antiepileptics - qtates - alleviation of acute anxiety and fear associated with transportation and veterinary visits.

Euroopan unioni - malta - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - massimu ta'tliet minn dawn li ġejjin purifikat, inattivat tal-marda tal-ilsien u d-dwiefer-virus tal-marda razez: o1 manisa ≥ 6 pd50*; o1 bfs ≥ 6 pd50*; o t-tajwan 3/97 ≥ 6 pd50*; a22-iraq ≥ 6 pd50*; a24 cruzeiro ≥ 6 pd50*; turkija 14/98 ≥ 6 pd50*; l-asja 1 shamir ≥ 6 pd50*; sat2 l-għarabja sawdita ≥ 6 pd50*; * pd50 – 50% protettiv-doża fl-ifrat kif deskritt fil-ph. eur. monografija 0063. - immunoloġiċi - pigs; cattle; sheep - immunizzazzjoni attiva ta 'baqar, nagħaġ u majjali minn età ta' 2 ġimgħat kontra l-marda ta 'l-ilsien u d-dwiefer biex jitnaqqsu s-sinjali kliniċi.

Euroopan unioni - malta - EMA (European Medicines Agency)

zoetis belgium sa - oclacitinib maleate - aġenti għad-dermatite, esklużi kortikosterojdi - klieb - - treatment of pruritus associated with allergic dermatitis in dogs. - treatment of clinical manifestations of atopic dermatitis in dogs.