XICLAV 1,2 g 1000 mg/1 viala+ 200 mg/1 viala prašak za rastvor za injekciju Bosnia dan Herzegovina - Kroasia - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

xiclav 1,2 g 1000 mg/1 viala+ 200 mg/1 viala prašak za rastvor za injekciju

sandoz d.o.o. - amoksicilin, klavulanska kiselina - prašak za rastvor za injekciju - 1000 mg/1 viala+ 200 mg/1 viala - 1 bočica sadrži: 1000 mg amoksicilina (u obliku amoksicilinnatrijuma) + 200 mg klavulanske kiseline (u obliku kalijumklavulanata)

PIPERACILLINTAZOBACTAM PANPHARMA 4 g + 500 mg Prašak za rastvor za infuziju Montenegro - Kroasia - CInMED-Institut za ljekove i medicinska sredstva Crne Gore

piperacillintazobactam panpharma 4 g + 500 mg prašak za rastvor za infuziju

"farmont m.p." d.o.o. za proizvodnju, promet i usluge, export-import danilovgrad - piperacilin, tazobaktam - prašak za rastvor za infuziju - 4 g + 500 mg

Cayston Uni Eropa - Kroasia - EMA (European Medicines Agency)

cayston

gilead sciences ireland uc - aztreonam lizin - cystic fibrosis; respiratory tract infections - antibakterijski lijekovi za sistemsku primjenu, - cayston je naznačeno za supresivna terapija kronične plućne infekcije zbog pseudomonas aeruginosa u bolesnika s cističnom fibrozom (cf) u dobi od 6 godina i starije. treba uzeti u obzir formalne preporuke za odgovarajuće korištenje antibakterijskih posrednika.

Ecalta Uni Eropa - Kroasia - EMA (European Medicines Agency)

ecalta

pfizer europe ma eeig - anidulafungin - kandidijaza - antimikotika za sustavnu uporabu - liječenje od invazivnog kandidijaze kod odraslih i pedijatrijska bolesnika u dobi od 1 mjeseca do < 18 godina.

Mycamine Uni Eropa - Kroasia - EMA (European Medicines Agency)

mycamine

astellas pharma europe b.v. - micafungin - kandidijaza - antimikotika za sustavnu uporabu - Микамин indiciran za:odrasli, adolescenti ≥ 16 godina i elderlytreatment od invazivnog kandidijaza;liječenje kandidijaza jednjaka u bolesnika za koje внутривенная terapija;prevencija candida infekcije kod pacijenata koji su patili аллогенную transplantaciju гемопоэтических matičnih stanica ili transplantacije pacijenti, koji, kako se očekuje, нейтропении (apsolutni broj neutrofila < 500 stanica/μl) u roku od 10 dana ili više. djecu (uključujući i novorođenčad) i teen < 16 godina agetreatment od invazivnog kandidijaza. prevencija candida infekcije kod pacijenata koji su patili аллогенную transplantaciju гемопоэтических matičnih stanica ili transplantacije pacijenti, koji, kako se očekuje, нейтропении (apsolutni broj neutrofila < 500 stanica/μl) u roku od 10 dana ili više. rješenje koristiti lijek Микамин treba uzeti u obzir potencijalni rizik od razvoja tumora jetre . tako Микамин treba primijeniti samo ako su drugi antifungalni lijekovi nisu prikladni.

Noxafil Uni Eropa - Kroasia - EMA (European Medicines Agency)

noxafil

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.

Vantobra Uni Eropa - Kroasia - EMA (European Medicines Agency)

vantobra

pari pharma gmbh - Тобрамицин - cystic fibrosis; respiratory tract infections - antibakterijski lijekovi za sistemsku primjenu, , Аминогликозидные antibakterijski lijekovi - vantobra je indiciran za liječenje kronične plućne infekcije zbog pseudomonas aeruginosa u bolesnika starijih od 6 godina i starijih s cističnom fibrozom (cf). treba uzeti u obzir formalne preporuke za odgovarajuće korištenje antibakterijskih posrednika.

Acipirin 4 g/0,5 g prašak za otopinu za infuziju Kroasia - Kroasia - HALMED (Agencija za lijekove i medicinske proizvode)

acipirin 4 g/0,5 g prašak za otopinu za infuziju

pliva hrvatska d.o.o., prilaz baruna filipovića 25, zagreb, hrvatska - piperacilinnatrij tazobaktamnatrij - prašak za otopinu za infuziju - 4,0 g + 0,5 g/bočica - urbroj: jedna bočica sadrži 4,0 g piperacilina u obliku piperacilinnatrija i 0,5 g tazobaktama u obliku tazobaktamnatrija

Anidulafungin Pliva 100 mg prašak za koncentrat za otopinu za infuziju Kroasia - Kroasia - HALMED (Agencija za lijekove i medicinske proizvode)

anidulafungin pliva 100 mg prašak za koncentrat za otopinu za infuziju

pliva hrvatska d.o.o., prilaz baruna filipovića 25, zagreb, hrvatska - anidulafungin - prašak za koncentrat za otopinu za infuziju - 100 mg - urbroj: jedna bočica sadrži 100 mg anidulafungina

Augmentin 400 mg + 57 mg/5 ml prašak za oralnu suspenziju Kroasia - Kroasia - HALMED (Agencija za lijekove i medicinske proizvode)

augmentin 400 mg + 57 mg/5 ml prašak za oralnu suspenziju

glaxosmithkline d.o.o., ulica damira tomljanovića gavrana 15, zagreb - amoksicilin trihidrat, kalijev klavulanat - prašak za oralnu suspenziju - 400 mg + 57 mg/5 ml - urbroj: nakon rekonstitucije, 1 ml oralne suspenzije sadrži 80 mg amoksicilina u obliku amoksicilin trihidrata i 11,4 mg klavulanske kiseline u obliku kalijevog klavulanata