Unione Europea - sloveno - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - attenuated feline panleucopenia virus (pli iv) - 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;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.

Unione Europea - sloveno - 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.

Unione Europea - sloveno - 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 chlamydophila felis (905 strain), attenuated feline panleucopenia virus (pli iv) - 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;• against chlamydophila felis infection to reduce clinical signs;• against feline panleucopenia to prevent mortality and clinical signs. nastopi imunosti so dokazali en teden po primarno cepljenje seveda za rhinotracheitis, calicivirus, chlamydophila felis in panleucopenia komponente. the duration of immunity is one year after the last re-vaccination for the chlamydiosis component, and oneyear after primary vaccination and three years after the last re-vaccination for the rhinotracheitis, calicivirosis and panleucopenia components.

Unione Europea - sloveno - 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), 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;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.

Unione Europea - sloveno - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - telmisartan - zastopniki, ki delujejo na renin-angiotensin sistem, angiotensin ii antagonisti, navaden - mačke - zmanjšanje proteinurije, povezane s kronično ledvično boleznijo (ckd).

Unione Europea - sloveno - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - rekombinantne turčija herpesvirus, sev vhvt013-69, v živo - immunologicals za aves, domačo kokošjo, immunologicals - embryonated eggs; chicken - za aktivno imunizacijo piščancev:Če želite preprečiti, umrljivost in zmanjšati klinični znaki in poškodb nalezljivih bolezni bursal. za zmanjšanje umrljivosti, klinični znaki in poškodbah marek je bolezen.

Unione Europea - sloveno - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - gamitromicin - antibakterij za sistemsko uporabo - cattle; pigs; sheep - cattletreatment in metaphylaxis goved, bolezni dihal (brd), ki je povezana z mannheimia haemolytica, pasteurella multocida in histophilus somni. prisotnost bolezni v čredi je treba določiti pred metafilaktično uporabo. pigstreatment prašičje bolezni dihal (srd), ki je povezana z actinobacillus pleuropneumoniae, pasteurella multocida, haemophilus parasuis in bordetella bronchiseptica. sheeptreatment nalezljivih pododermatitis (stopala gnilobe), ki je povezana s sovražno dichelobacter nodosus in fusobacterium necrophorum, ki zahteva sistemsko zdravljenje.

Unione Europea - sloveno - EMA (European Medicines Agency)

boehringer ingelheim international gmbh - empagliflozin - diabetes mellitus, type 2; heart failure; renal insufficiency, chronic - zdravila, ki se uporabljajo pri diabetesu - type 2 diabetes mellitusjardiance is indicated for the treatment of adults with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exerciseas monotherapy when metformin is considered in addition to other medicinal products for the treatment of diabetesfor study results with respect to combinations of therapies, effects on glycaemic control, and cardiovascular and renal events, and the populations studied, see sections 4. 4, 4. 5 in 5. of the annex. heart failurejardiance is indicated in adults for the treatment of symptomatic chronic heart failure.  chronic kidney diseasejardiance is indicated in adults for the treatment of chronic kidney disease.

Unione Europea - sloveno - EMA (European Medicines Agency)

boehringer ingelheim international gmbh - nintedanib - idiopatska pljučna fibroza - antineoplastična sredstva - ofev je indiciran pri odraslih za zdravljenje idiopatske pljučne fibroze (ipf).

Unione Europea - sloveno - EMA (European Medicines Agency)

boehringer ingelheim international gmbh - nintedanib - karcinom, pljučni pljuč - antineoplastična sredstva - vargatef je naveden v kombinaciji z docetaxel za zdravljenje odraslih bolnikov z lokalno napredovalim in metastatskim lokalno ponavljajoče se nedrobnoceličnim rakom pljuč (nsclc) adenokarcinoma tumor histologijo po prvi vrstici kemoterapijo.