Europska Unija - hrvatski - EMA (European Medicines Agency)

virbac s.a. - purified p45 feline leukaemia virus envelope antigen, live feline calicivirus (strain f9), live feline viral rhinotracheitis virus (strain f2), live feline panleucopenia virus - živjeti panleucopenia virus mačke / парвовирусный + video mačke, virus ринотрахеита + video mačji калицивирус + инактивированный virus leukemije mačaka - mačke - za aktivnu imunizaciju mačaka od osam tjedana protiv: mačji kalicivirozu kako bi se smanjili klinički znakovi. mačji virusni ринотрахеит za smanjenje kliničkih znakova i izlučivanje virusa. mačke panleucopenije kako bi se spriječila leukopenija i smanjili klinički znakovi. mačje leukemije kako bi se spriječila uporna viremija i klinički znakovi povezane bolesti. početak imuniteta: 3 tjedna nakon primarne cijepljenja za komponente panleucopenije i leukemije i 4 tjedna nakon primarne cijepljenja za virusne komponente kalicivirusnih i rinotraheitisa. trajanje imuniteta: jedna godina nakon primarne cijepljenja za sve sastojke.

Europska Unija - hrvatski - EMA (European Medicines Agency)

virbac s.a. - pročišćenog p45 felv-envelope antigena - Инактивированные virusnih cjepiva, virus mačje leukemije, imunomodulatori za mačke, - mačke - aktivna imunizacija mačaka od osam tjedana protiv mačje leukemije radi sprečavanja perzistirajuće viremije i kliničkih znakova povezane bolesti.

Europska Unija - hrvatski - EMA (European Medicines Agency)

virbac s.a. - pročišćenog rp-45 felv-envelope antigena - Инактивированные virusna cjepiva - mačke - aktivna imunizacija mačaka od osam tjedana protiv mačje leukemije radi sprečavanja perzistirajuće viremije i kliničkih znakova povezane bolesti.

Europska Unija - hrvatski - 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) - imunomodulatori za mačke, - 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.

Europska Unija - hrvatski - 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) - imunomodulatori za mačke, - 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.

Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

accord healthcare polska sp. z o.o., ul. tasmowa 7, mazowieckie, varšava, poljska - dutasteridum, tamsulosinum - kapsula, tvrda - 0,5 mg + 0,4 mg - urbroj: svaka kapsula sadrži 0,5 mg dutasterida i 0,4 mg tamsulozinklorida (ekvivalentno 0,367 mg tamsulozina)

Europska Unija - hrvatski - EMA (European Medicines Agency)

novartis europharm limited  - gozetotide - radionuklidno slikanje - dijagnostički radiofarmaceutici - ovaj je lijek samo za dijagnostičku uporabu. locametz, after radiolabelling with gallium 68, is indicated for the detection of prostate specific membrane antigen (psma) positive lesions with positron emission tomography (pet) in adults with prostate cancer (pca) in the following clinical settings:primary staging of patients with high risk pca prior to primary curative therapy,suspected pca recurrence in patients with increasing levels of serum prostate specific antigen (psa) after primary curative therapy,identification of patients with psma positive progressive metastatic castration resistant prostate cancer (mcrpc) for whom psma targeted therapy is indicated (see section 4.

Europska Unija - hrvatski - EMA (European Medicines Agency)

amicus therapeutics europe limited - cipaglucosidase alfa - vrsta ii za skladištenje glikogena - drugi gastrointestinalni trakt i metabolizam, lijekovi, - pombiliti (cipaglucosidase alfa) is a long-term enzyme replacement therapy used in combination with the enzyme stabiliser miglustat for the treatment of adults with late-onset pompe disease (acid α-glucosidase [gaa] deficiency).

Europska Unija - hrvatski - EMA (European Medicines Agency)

laboratorios hipra, s.a. - mycoplasma hyopneumoniae, strain 7304 (nexhyon), expressing the capsid protein of porcine circovirus type 2a, inactivated - immunologicals for suidae, inactivated viral and inactivated bacterial vaccines - svinje - for the active immunisation of pigs:to reduce lung lesions associated with porcine enzootic pneumonia caused by mycoplasma hyopneumoniae. also, to reduce the incidence of these lesions (as observed in field studies). to reduce viraemia, virus load in lungs and lymphoid tissues and the duration of the viraemic period associated with diseases caused by porcine circovirus type 2 (pcv2). efficacy against pcv2 genotypes a, b and d has been demonstrated in field studies. to reduce culling rate and the loss of daily weight gain caused by mycoplasma hyopneumoniae and/or pcv2 related diseases (as observed at 6 months of age in field studies). mycoplasma hyopneumoniae: onset of immunity: 3 weeks after vaccinationduration of immunity: 23 weeks after vaccinationporcine circovirus type 2:onset of immunity: 2 weeks after vaccinationduration of immunity: 22 weeks after vaccinationin addition, a reduction in nasal and faecal shedding and the duration of nasal excretion of pcv2 was demonstrated in animals challenged at 4 weeks and at 22 weeks after vaccination.

Europska Unija - hrvatski - EMA (European Medicines Agency)

ucb pharma sa  - Цертолизумаб pegol - artritis, reumatoidni - imunosupresivi - reumatoidni arthritiscimzia, u kombinaciji sa metotreksatom (mtx), prikazan je za:liječenje umjereni do teški, aktivni reumatoidni artritis (ra) kod odraslih pacijenata, kada je u odgovoru na заболевани-razrađen antirheumatic napitke (dmards), uključujući i metotreksat, bio je neadekvatno. cimzia može biti dano kao monoterapija u slučaju netolerancije na mtx ili pri nastavak liječenja s mtx je inappropriatethe liječenje teških, aktivnog i uznapredovalog ra kod odraslih, koji nisu prethodno tretirani s mtx ili drugim lijekovima базисными. cimzia je pokazala da smanjuju brzinu progresije poraza zglobova, mjerene x-zračenja i poboljšati fizičku funkciju, kada se daje u kombinaciji s mtx. Аксиальный спондилоартрит cimzia indiciran za liječenje odraslih bolesnika s teškim aktivnim аксиальным спондилоартритом, uključujući:ankilozantni spondilitis (as)odrasle osobe s teškim aktivnim анкилозирующим спондилитом koji su imali neadekvatan odgovor ili netoleranciju nesteroidni protuupalni lijekovi (nsar). Аксиальный спон