Hrvatska - hrvatski - Ministarstvo poljoprivrede, Uprava za Veterinarstvo i sigurnost hrane

laboratorios syva, s.a.u., av/párroco pablo díez, 49-57, 24010 león, Španjolska - enrofloksacin - otopina za injekciju - antibakterijski vmp za sustavne infekcije - goveda i svinja

Hrvatska - hrvatski - Ministarstvo poljoprivrede, Uprava za Veterinarstvo i sigurnost hrane

laboratorios syva, s.a.u., avda. párroco pablo diez, 49-57, 24010 león, Španjolska - gonadorelin - otopina za injekciju - goveda (krave, junice)

Europska Unija - hrvatski - EMA (European Medicines Agency)

merck sharp and dohme b.v - posakonazol - candidiasis; mycoses; coccidioidomycosis; aspergillosis - antimikotika za sustavnu uporabu - noxafil gastro-resistant tablets are indicated for use in the treatment of the following fungal infections in adults (see sections 4. 2 i 5. 1):- invasive aspergillosisnoxafil gastro-resistant tablets are indicated for use in the treatment of the following fungal infections in paediatric patients from 2 years of age weighing more than 40 kg and adults (see sections  4. 2 i 5. 1):- invasive aspergillosis in patients with disease that is refractory to amphotericin b or itraconazole or in patients who are intolerant of these medicinal products;- fusariosis in patients with disease that is refractory to amphotericin b or in patients who are intolerant of amphotericin b;- chromoblastomycosis and mycetoma in patients with disease that is refractory to itraconazole or in patients who are intolerant of itraconazole;- coccidioidomycosis in patients with disease that is refractory to amphotericin b, itraconazole or fluconazole or in patients who are intolerant of these medicinal products. Огнеупорность definira kao progresiju infekcije ili nedostatak poboljšanja nakon što je minimum 7 dana do terapijske doze učinkovit antifungalna terapija. noxafil gastro-resistant tablets are also indicated for prophylaxis of invasive fungal infections in the following paediatric patients from 2 years of age weighing more than 40 kg and adults (see sections 4. 2 i 5. 1):- patients receiving remission-induction chemotherapy for acute myelogenous leukaemia (aml) or myelodysplastic syndromes (mds) expected to result in prolonged neutropenia and who are at high risk of developing invasive fungal infections;- hematopoietic stem cell transplant (hsct) recipients who are undergoing high-dose immunosuppressive therapy for graft versus host disease and who are at high risk of developing invasive fungal infections. please refer to the summary of product characteristics of noxafil oral suspension for use in oropharyngeal candidiasis.  noxafil concentrate for solution for infusion is indicated for use in the treatment of the following fungal infections in adults (see sections 4. 2 i 5. 1):- invasive aspergillosisnoxafil concentrate for solution for infusion is indicated for use in the treatment of the following fungal infections in adult and paediatric patients from 2 years of age (see sections 4. 2 i 5. 1):- invasive aspergillosis in patients with disease that is refractory to amphotericin b or itraconazole or in patients who are intolerant of these medicinal products;- fusariosis in patients with disease that is refractory to amphotericin b or in patients who are intolerant of amphotericin b;- chromoblastomycosis and mycetoma in patients with disease that is refractory to itraconazole or in patients who are intolerant of itraconazole;- coccidioidomycosis in patients with disease that is refractory to amphotericin b, itraconazole or fluconazole or in patients who are intolerant of these medicinal products. Огнеупорность definira kao progresiju infekcije ili nedostatak poboljšanja nakon što je minimum 7 dana do terapijske doze učinkovit antifungalna terapija. noxafil concentrate for solution for infusion is also indicated for prophylaxis of invasive fungal infections in the following adult and paediatric patients from 2 years of age (see sections 4. 2 i 5. 1):- patients receiving remission-induction chemotherapy for acute myelogenous leukaemia (aml) or myelodysplastic syndromes (mds) expected to result in prolonged neutropenia and who are at high risk of developing invasive fungal infections;- hematopoietic stem cell transplant (hsct) recipients who are undergoing high-dose immunosuppressive therapy for graft versus host disease (gvhd) and who are at high risk of developing invasive fungal infections. please refer to the summary of product characteristics of noxafil oral suspension for use in oropharyngeal candidiasis.  noxafil gastro resistant powder and solvent for oral suspension is indicated for use in the treatment of the following fungal infections in paediatric patients from 2 years of age (see sections 4. 2 i 5. 1):- invasive aspergillosis in patients with disease that is refractory to amphotericin b or itraconazole or in patients who are intolerant of these medicinal products;- fusariosis in patients with disease that is refractory to amphotericin b or in patients who are intolerant of amphotericin b;- chromoblastomycosis and mycetoma in patients with disease that is refractory to itraconazole or in patients who are intolerant of itraconazole;- coccidioidomycosis in patients with disease that is refractory to amphotericin b, itraconazole or fluconazole or in patients who are intolerant of these medicinal products. Огнеупорность definira kao progresiju infekcije ili nedostatak poboljšanja nakon što je minimum 7 dana do terapijske doze učinkovit antifungalna terapija. noxafil gastro-resistant powder and solvent for oral suspension is indicated for prophylaxis of invasive fungal infections in the following paediatric patients from 2  years of age:- patients receiving remission-induction chemotherapy for acute myelogenous leukaemia (aml) or myelodysplastic syndromes (mds) expected to result in prolonged neutropenia and who are at high  risk of developing invasive fungal infections;- haematopoietic stem cell transplant (hsct) recipients who are undergoing high-dose immunosuppressive therapy for graft versus host disease and who are at high  risk of developing invasive fungal infections. please refer to the summary of product characteristics of noxafil concentrate for solution for infusion and the gastro-resistant tablets for use in primary treatment of invasive aspergillosis. please refer to the summary of product characteristics of noxafil oral suspension for use in oropharyngeal candidiasis.  noxafil oral suspension is indicated for use in the treatment of the following fungal infections in adults (see section 5. 1):- invasive aspergillosis in patients with disease that is refractory to amphotericin b or itraconazole or in patients who are intolerant of these medicinal products;- fusariosis in patients with disease that is refractory to amphotericin b or in patients who are intolerant of amphotericin b;- chromoblastomycosis and mycetoma in patients with disease that is refractory to itraconazole or in patients who are intolerant of itraconazole;- coccidioidomycosis in patients with disease that is refractory to amphotericin b, itraconazole or fluconazole or in patients who are intolerant of these medicinal products;- oropharyngeal candidiasis: as first-line therapy in patients who have severe disease or are immunocompromised, in whom response to topical therapy is expected to be poor. Огнеупорность definira kao progresiju infekcije ili nedostatak poboljšanja nakon što je minimum 7 dana do terapijske doze učinkovit antifungalna terapija. noxafil oral suspension is also indicated for prophylaxis of invasive fungal infections in the following patients:- patients receiving remission-induction chemotherapy for acute myelogenous leukaemia (aml) or myelodysplastic syndromes (mds) expected to result in prolonged neutropenia and who are at high risk of developing invasive fungal infections;- hematopoietic stem cell transplant (hsct) recipients who are undergoing high-dose immunosuppressive therapy for graft versus host disease and who are at high risk of developing invasive fungal infections. please refer to the summary of product characteristics of noxafil concentrate for solution for infusion and the gastro-resistant tablets for use in primary treatment of invasive aspergillosis.

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

kardian d.o.o. hondlova 2/9 10000 zagreb -

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

glaxosmithkline dungarvan ltd., knockbrack, dungarvan, county waterford, irska - paracetamol fenilefrinklorid gvaifenezin - kapsula, tvrda - 500 mg + 6,1 mg + 100 mg - urbroj: svaka kapsula sadrži 500 mg paracetamola, 6,1 mg fenilefrinklorida (što odgovara 5 mg fenilefrin baze) i 100 mg gvaifenezina

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

glaxosmithkline dungarvan ltd., knockbrack, dungarvan, county waterford, irska - paracetamol - filmom obložena tableta - 500 mg - urbroj: jedna tableta sadrži 500 mg paracetamola

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

glaxosmithkline dungarvan ltd., knockbrack, dungarvan, county waterford, irska - paracetamol fenilefrinklorid gvaifenezin - prašak za oralnu otopinu - 1000 mg + 12,2 mg + 200 mg - urbroj: svaka jednodozna vrećica sadrži 1000 mg paracetamola, 12,2 mg fenilefrinklorida (što odgovara 10 mg fenilefrin baze) i 200 mg gvaifenezina

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

fresenius kabi d.o.o., radnička cesta 37a, zagreb, hrvatska - levobupivakainklorid - otopina za injekciju/infuziju - 5 mg/ml - urbroj: 1 ml otopine sadrži 5 mg levobupivakaina u obliku levobupivakainklorida

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

fresenius kabi d.o.o., radnička cesta 37a, zagreb, hrvatska - glukoza hidrat - otopina za infuziju - 50 g/1000 ml - urbroj: 1 ml otopine za infuziju sadrži 50,0 mg glukoze, bezvodne (u obliku 55,0 mg glukoza hidrata) 1000 ml otopine za infuziju sadrži 50,0 g glukoze, bezvodne (u obliku 55,0 g glukoza hidrata)

Europska Unija - hrvatski - EMA (European Medicines Agency)

laboratorios syva, s.a.u. - Инактивированный virus катаральной groznice ovaca, серотипы 1, soj alg2006/01 e1, инактивированный virus блютанг, серотип 4, soj bt-4/spa-1/2004, инактивированный virus блютанг, серотип 8, soj bel2006/01 - Инактивированные virusna cjepiva - cattle; sheep - za aktivne imunizacije ovaca kako bi se spriječilo вирусемии i smanjenje kliničkih znakova i lezije uzrokovane virusa блютанга серотипа 1 i/ili 8 i/ili smanjenje виремии* i kliničkih znakova i lezije uzrokovane virusom блютанга серотипа 4для aktivna imunizacija goveda za prevenciju виремии, zbog virusa блютанга серотипа 1 i/ili 8 i/ili za smanjenje вирусемии* uzrokovane virusa блютанга серотипа 4.