Nuedexta Europska Unija - hrvatski - EMA (European Medicines Agency)

nuedexta

jenson pharmaceutical services limited - dextromethorphan, kinidin - neuronske manifestacije - ostali lijekovi protiv živčanog sustava - nuedexta je indiciran za simptomatsko liječenje pseudobulbarskih učinaka (pba) u odraslih osoba. učinkovitost je ispitivana samo u bolesnika s temeljnom amiloidnom lateralnom sklerozom ili multipla sklerozom.

Fareston Europska Unija - hrvatski - EMA (European Medicines Agency)

fareston

orion corporation - toremifen - neoplazme dojki - endokrinska terapija - prva linija hormonskog liječenja raka dojke ovisna o hormonima u bolesnika u postmenopauzi. Фарестон ne preporučuje se za pacijente sa estrogen receptor negativnih tumora.

Olmesartan/hidroklorotiazid Genericon 20 mg/12,5 mg filmom obložene tablete Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

olmesartan/hidroklorotiazid genericon 20 mg/12,5 mg filmom obložene tablete

genericon pharma gesellschaft m.b.h., hafnerstraße 211, graz, austrija - olmesartanmedoksomil hidroklorotiazid - filmom obložena tableta - 20 mg + 12,5 mg - urbroj: jedna tableta sadrži 20 mg olmesartanmedoksomila i 12,5 mg hidroklorotiazida

Olmesartan/hidroklorotiazid Genericon 20 mg/25 mg filmom obložene tablete Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

olmesartan/hidroklorotiazid genericon 20 mg/25 mg filmom obložene tablete

genericon pharma gesellschaft m.b.h., hafnerstraße 211, graz, austrija - olmesartanmedoksomil hidroklorotiazid - filmom obložena tableta - 20 mg + 25 mg - urbroj: jedna tableta sadrži 20 mg olmesartanmedoksomila i 25 mg hidroklorotiazida

Olmesartan/hidroklorotiazid Genericon 40 mg/12,5 mg filmom obložene tablete Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

olmesartan/hidroklorotiazid genericon 40 mg/12,5 mg filmom obložene tablete

genericon pharma gesellschaft m.b.h., hafnerstraße 211, graz, austrija - olmesartanmedoksomil hidroklorotiazid - filmom obložena tableta - 40 mg + 12,5 mg - urbroj: jedna tableta sadrži 40 mg olmesartanmedoksomila i 12,5 mg hidroklorotiazida

Olmesartan/hidroklorotiazid Genericon 40 mg/25 mg filmom obložene tablete Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

olmesartan/hidroklorotiazid genericon 40 mg/25 mg filmom obložene tablete

genericon pharma gesellschaft m.b.h., hafnerstraße 211, graz, austrija - olmesartanmedoksomil hidroklorotiazid - filmom obložena tableta - 40 mg + 25 mg - urbroj: jedna tableta sadrži 40 mg olmesartanmedoksomila i 25 mg hidroklorotiazida

Noxafil Europska Unija - hrvatski - 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.

GASTROPERIDON 10 mg/1 tableta tableta Bosna i Hercegovina - hrvatski - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

gastroperidon 10 mg/1 tableta tableta

hemofarm proizvodnja farmaceutskih proizvoda d.o.o. banja luka - домперидон - tableta - 10 mg/1 tableta - 1 tableta sadrži: 10 mg domperidona (u obliku domperidonmaleata)

Rasilamlo Europska Unija - hrvatski - EMA (European Medicines Agency)

rasilamlo

novartis europharm ltd - алискирена, амлодипина - hipertenzija - sredstva koja djeluju na sustav renin-angiotenzina - rasilamlo je indiciran za liječenje esencijalne hipertenzije u odraslih bolesnika čiji krvni tlak nije odgovarajuće kontroliran sa lijekovima ili amlodipin koristiti samo.

Rasilez Europska Unija - hrvatski - EMA (European Medicines Agency)

rasilez

noden pharma dac - aliskiren - hipertenzija - sredstva koja djeluju na sustav renin-angiotenzina - liječenje esencijalne hipertenzije.