Europska Unija - hrvatski - EMA (European Medicines Agency)

novartis europharm limited - imatinib - precursor cell lymphoblastic leukemia-lymphoma; gastrointestinal stromal tumors; dermatofibrosarcoma; myelodysplastic-myeloproliferative diseases; leukemia, myelogenous, chronic, bcr-abl positive; hypereosinophilic syndrome - antineoplastična sredstva - glivec is indicated for the treatment of , adult and paediatric patients with newly diagnosed philadelphia-chromosome (bcr-abl)-positive (ph+) chronic myeloid leukaemia (cml) for whom bone-marrow transplantation is not considered as the first line of treatment;, adult and paediatric patients with ph+ cml in chronic phase after failure of interferon-alpha therapy, or in accelerated phase or blast crisis;, adult and paediatric patients with newly diagnosed philadelphia-chromosome-positive acute lymphoblastic leukaemia (ph+ all) integrated with chemotherapy;, adult patients with relapsed or refractory ph+ all as monotherapy;, adult patients with myelodysplastic / myeloproliferative diseases (mds / mpd) associated with platelet-derived growth factor receptor (pdgfr) gene re-arrangements;, adult patients with advanced hypereosinophilic syndrome (hes) and / or chronic eosinophilic leukaemia (cel) with fip1l1-pdgfra rearrangement. učinak Гливека na ishod transplantacije koštane srži još nije određen. glivec is indicated for: , the treatment of adult patients with kit (cd 117)-positive unresectable and / or metastatic malignant gastrointestinal stromal tumours (gist);, the adjuvant treatment of adult patients who are at significant risk of relapse following resection of kit (cd117)-positive gist. pacijenti koji imaju niske ili vrlo nizak rizik recidiva ne bi trebali primati adjuvantne terapije; liječenje odraslih bolesnika s метастатической выбухающей dermatofibrosarcoma (dfsp) i odraslih pacijenata s relaps i / ili метастатической dfsp, koji nemaju pravo na operaciju. u odrasle osobe i pedijatrijska bolesnika, učinkovitosti glivec se temelji na zajedničkim гематологических i цитогенетических odgovora i preživljavanja bez progresije kod kml, na гематологический i цитогенетический odgovor cijene na ph+ all, mds / rafinerija, na гематологические indikatori odgovora u hes / cel i objektivnih odgovora kod odraslih pacijenata s неоперабельными i / ili метастатическими gist i dfsp i na безрецидивную stopa preživljavanja pri adjuvantne bit. iskustvo glivec u bolesnika s mds / rafinerija u svezi s pdgfr генных permutacija-vrlo ograničen (vidi odjeljak 5. osim po prvi put prijavljene kronične fazi kml, nema kontroliranih istraživanja pokazuju klinički učinak ili povećava stopu preživljavanja kod te bolesti.

Crna Gora - hrvatski - CInMED-Institut za ljekove i medicinska sredstva Crne Gore

pharmaswiss - montenegro, pharmaswiss doo beograd, dio stranog druŠtva u podgorici - tadalafil - film tableta - 20mg

Crna Gora - hrvatski - CInMED-Institut za ljekove i medicinska sredstva Crne Gore

pharmaswiss - montenegro, pharmaswiss doo beograd, dio stranog druŠtva u podgorici - tadalafil - film tableta - 10mg

Crna Gora - hrvatski - CInMED-Institut za ljekove i medicinska sredstva Crne Gore

pharmaswiss - montenegro, pharmaswiss doo beograd, dio stranog druŠtva u podgorici - tadalafil - film tableta - 5mg

Crna Gora - hrvatski - CInMED-Institut za ljekove i medicinska sredstva Crne Gore

"novartis pharma services ag" dio stranog druŠtva podgorica - imatinib - film tableta - 100mg

Crna Gora - hrvatski - CInMED-Institut za ljekove i medicinska sredstva Crne Gore

"novartis pharma services ag" dio stranog druŠtva podgorica - imatinib - film tableta - 400mg

Crna Gora - hrvatski - CInMED-Institut za ljekove i medicinska sredstva Crne Gore

"novartis pharma services ag" dio stranog druŠtva podgorica - imatinib - kapsula, tvrda - 100mg

Europska Unija - hrvatski - EMA (European Medicines Agency)

laboratorios hipra s.a - živjeti ets - tk - dual-gen-uklonjen goveđi herpes virus tip 1, soj ceddel: 106.3–107.3 ccid50 - immunologicals - stoka - za aktivna imunizacija goveda s tri mjeseca starosti goveda protiv virusa herpesa tipa 1 (bohv-1) za smanjenje kliničkih znakova infekcije ринотрахеита goveda (ИБР) i polje virus izlučivanje. početak imuniteta: 21 dan nakon završetka osnovne sheme cijepljenja. trajanje imuniteta: 6 mjeseci nakon završetka osnovne sheme cijepljenja .

Europska Unija - hrvatski - 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 - svinje - za aktivnu imunizaciju svinja od sedam tjedana pa nadalje kako bi se spriječila smrtnost i smanjila infekcija i bolesti uzrokovane virusom klasične svinjske kuge (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.

Europska Unija - hrvatski - EMA (European Medicines Agency)

ceva-phylaxia co. ltd. - live recombinant fowlpox virus expressing the membrane fusion protein and the encapsidation protein of avian infectious laryngotracheitis virus (rfp-lt) and avian encephalomyelitis virus, strain calnek 1143 (ae) - immunologicals for aves, live viral vaccines, domestic fowl - piletina - for active immunisation of chickens of 8 to 13 weeks of age in order to reduce the skin lesions due to fowlpox, to reduce the clinical signs and tracheal lesions due to avian infectious laryngotracheitis and to prevent egg production losses due to avian encephalomyelitis.