Unia Europejska - słoweński - EMA (European Medicines Agency)

pfizer limited - sunitinib - gastrointestinal stromal tumors; carcinoma, renal cell; neuroendocrine tumors - antineoplastična sredstva - gastrointestinal stromal tumour (gist)sutent is indicated for the treatment of unresectable and/or metastatic malignant gastrointestinal stromal tumour (gist) in adults after failure of imatinib mesilate treatment due to resistance or intolerance. metastatic renal cell carcinoma (mrcc)sutent is indicated for the treatment of advanced/metastatic renal cell carcinoma (mrcc) in adults. pancreatic neuroendocrine tumours (pnet)sutent is indicated for the treatment of unresectable or metastatic, well-differentiated pancreatic neuroendocrine tumours with disease progression in adults. experience with sutent as first-line treatment is limited (see section 5.

Unia Europejska - słoweński - EMA (European Medicines Agency)

elanco gmbh - lotilaner - ectoparasiticides za sistemsko uporabo, isoxazolines - dogs; cats - za zdravljenje bolh in klopi infestations. bolhe in klopi mora priložiti gostiteljice in začne hranjenje, da bi izpostavljene aktivni snovi,. zdravilo za uporabo v veterinarski medicini se lahko uporablja kot del strategije zdravljenja za nadzor alergijskega dermatitisa bolha (fad). dogsthis zdravila zagotavlja takojšnje in dolgotrajne ubijanje dejavnosti za 1 mesec za bolhe (ctenocephalides felis in c. canis) in klopi (rhipicephalus sanguineus, ixodes ricinus, i. hexagonus in dermacentor reticulatus). catsthis zdravila zagotavlja takojšnje in dolgotrajne ubijanje dejavnosti za 1 mesec pred bolhe (ctenocephalides felis in c. canis) in klopi (ixodes ricinus).

Unia Europejska - słoweński - EMA (European Medicines Agency)

accord healthcare s.l.u. - sunitinib - gastrointestinal stromal tumors; carcinoma, renal cell; neuroendocrine tumors - antineoplastična sredstva - gastrointestinal stromal tumour (gist)sunitinib accord is indicated for the treatment of unresectable and/or metastatic malignant gastrointestinal stromal tumour (gist) in adults after failure of imatinib treatment due to resistance or intolerance. metastatic renal cell carcinoma (mrcc)sunitinib accord is indicated for the treatment of advanced/metastatic renal cell carcinoma (mrcc) in adults. pancreatic neuroendocrine tumours (pnet)sunitinib accord is indicated for the treatment of unresectable or metastatic, well-differentiated pancreatic neuroendocrine tumours (pnet) with disease progression in adults.

Unia Europejska - słoweński - EMA (European Medicines Agency)

intervet international bv - indoxacarb, permethrin - permethrin, kombinacije, ectoparasiticides za lokalno uporabo, vključno. insekticidi - psi - zdravljenje infestacij bolh (ctenocephalides felis); izdelek ima trajno insekticidno učinkovitost do 4 tedne proti ctenocephalides felis. zdravilo ima trajno akaricidno učinkovitost do 5 tednov proti ixodes ricinusu in do 3 tedne proti rhipicephalus sanguineus. ena obdelava zagotavlja repelentno (anti-hranjenje) aktivnost proti peskom (phlebotomus perniciosus) do 3 tedne.

Unia Europejska - słoweński - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - največ tri od naslednjih prečiščeni, inaktivirano slinavke in parkljevke virus sevov: o1 manisa ≥ 6 pd50*; o1 bfs ≥ 6 pd50*; o tajvanu, 3/97 ≥ 6 pd50*; a22 iraku ≥ 6 pd50*; a24 cruzeiro ≥ 6 pd50*; puranji 14/98 ≥ 6 pd50*; azija 1 shamir ≥ 6 pd50*; sat2 savdska arabija ≥ 6 pd50*; * pd50 – 50% zaščitni odmerek goveda, kot je opisano v doktor tehniških znanosti eur. monografija 0063. - imunologija - pigs; cattle; sheep - aktivna imunizacija goveda, ovac in prašičev od 2 tedna starosti proti slinavki in parkljevki za zmanjšanje kliničnih znakov.

Unia Europejska - słoweński - EMA (European Medicines Agency)

intervet international bv - inaktiviran himejski sev flavivirusa yf-wn - imunologija - konji - aktivna imunizacija konj proti virusu west nile (wnv) za zmanjšanje kliničnih znakov bolezni in lezij v možganih ter za zmanjšanje viremije. začetek imunosti: 2 tedna po osnovnem cepljenju dveh injekcij. trajanje imunitete: 12 mesecev.

Unia Europejska - słoweński - EMA (European Medicines Agency)

merial s.a.s.  - inaktivirano gripa-virus, prašičev - imunologija - prašiči - aktivno imunizacijo prašičev v starosti od 56 dni naprej, vključno z noseča svinje proti prašičji gripi, ki jih povzročajo podtipov h1n1, h3n2 in h1n2 za zmanjšanje kliničnih znakov in virusnih pljuč obremenitev po okužbi. začetek imunosti: 7 dni po primarnem cepljenju. trajanje imunosti: 4 mesecih, v štrucah, cepljenih med starost 56 in 96 dni do 6 mesecev, v štrucah, cepljenih prvič na 96 dni in več. aktivna imunizacija nosečih svinj po končani primarni imunizaciji z dajanjem enega samega odmerka 14 dni pred prasitvijo razviti visoko kolostralno imunost, ki zagotavlja klinično zaščito pujskov vsaj 33 dni po rojstvu.

Unia Europejska - słoweński - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains) - immunologicals za skupin felidae, - mačke - 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.

Unia Europejska - słoweński - EMA (European Medicines Agency)

merial - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains), attenuated chlamydophila felis (905 strain) - immunologicals za skupin felidae, - mačke - active immunisation of cats aged 8 weeks and older:against feline viral rhinotracheitis to reduce clinical signs;against calicivirus infection to reduce clinical signs and excretion;against chlamydophila felis infection to reduce clinical signs. na imunski sistem je bil dokazan 1 teden po osnovnem cepljenju za rinotraheitis, kalicivirus in komponento chlamydophila felis. trajanje imunosti je 1 leto po zadnjem (ponovnem) cepljenju.

Unia Europejska - słoweński - EMA (European Medicines Agency)

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 za skupin felidae, - mačke - 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.