CINACALCET ACCORD 30 mg Romanya - Romence - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

cinacalcet accord 30 mg

ge pharmaceuticals ltd. - bulgaria - cinacalcetum - compr. film - 30mg - preparate antihormoni paratiroidieni medicamente antihormoni paratiroidieni

CINACALCET ACCORD 60 mg Romanya - Romence - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

cinacalcet accord 60 mg

ge pharmaceuticals ltd. - bulgaria - cinacalcetum - compr. film - 60mg - preparate antihormoni paratiroidieni medicamente antihormoni paratiroidieni

CINACALCET ACCORD 90 mg Romanya - Romence - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

cinacalcet accord 90 mg

ge pharmaceuticals ltd. - bulgaria - cinacalcetum - compr. film - 90mg - preparate antihormoni paratiroidieni medicamente antihormoni paratiroidieni

ACID ALENDRONIC/COLECALCIFEROL MYLAN 70 mg/2800 UI Romanya - Romence - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

acid alendronic/colecalciferol mylan 70 mg/2800 ui

ge pharmaceuticals ltd. - bulgaria - acid alendronicum+colecalciferolum - compr. - 70mg/2800ui - med. ce influenteaza in structura osoasa si mineralizare bifosfonati in combinatii

ACID ALENDRONIC/COLECALCIFEROL MYLAN 70 mg/5600 UI Romanya - Romence - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

acid alendronic/colecalciferol mylan 70 mg/5600 ui

ge pharmaceuticals ltd. - bulgaria - acid alendronicum+colecalciferolum - compr. - 70mg/5600ui - med. ce influenteaza in structura osoasa si mineralizare bifosfonati in combinatii

CINACALCET ACCORD 60 mg Romanya - Romence - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

cinacalcet accord 60 mg

ge pharmaceuticals ltd. - bulgaria - cinacalcetum - compr. film - 60mg - preparate antihormoni paratiroidieni medicamente antihormoni paratiroidieni

CINACALCET ACCORD 90 mg Romanya - Romence - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

cinacalcet accord 90 mg

ge pharmaceuticals ltd. - bulgaria - cinacalcetum - compr. film - 90mg - preparate antihormoni paratiroidieni medicamente antihormoni paratiroidieni

Noxafil Avrupa Birliği - Romence - EMA (European Medicines Agency)

noxafil

merck sharp and dohme b.v - posaconazol - candidiasis; mycoses; coccidioidomycosis; aspergillosis - antimicotice pentru uz sistemic - noxafil gastro-resistant tablets are indicated for use in the treatment of the following fungal infections in adults (see sections 4. 2 și 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 și 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. refractară este definită ca progresie a infecției sau eșecul de a îmbunătăți dupa o perioada de minim 7 zile înainte de eficient la doze terapeutice tratamentul antifungic. 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 și 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 și 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 și 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. refractară este definită ca progresie a infecției sau eșecul de a îmbunătăți dupa o perioada de minim 7 zile înainte de eficient la doze terapeutice tratamentul antifungic. 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 și 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 și 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. refractară este definită ca progresie a infecției sau eșecul de a îmbunătăți dupa o perioada de minim 7 zile înainte de eficient la doze terapeutice tratamentul antifungic. 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):- aspergiloză invazivă la pacienții cu boală rezistentă la amfotericina b sau itraconazol sau la pacienți care nu tolerează aceste medicamente;- fuzarioză la pacienții cu boală rezistentă la amfotericina b sau itraconazol sau la pacienți care nu tolerează amfotericina b;- cromoblastomicoză și micetom la pacienții cu boală rezistentă la itraconazol sau la pacienți care prezintă intoleranță la itraconazol;- coccidioidomicoză la pacienții cu boală rezistentă la amfotericina b, itraconazol sau fluconazol sau la pacienții care au intoleranță la aceste medicamente;- candidoza oro-faringiană: ca terapie de prima linie la pacienții care au boli grave sau sunt imunocompromiși, în care, ca răspuns la terapia topică este de așteptat să fie săraci. refractară este definită ca progresie a infecției sau eșecul de a îmbunătăți dupa o perioada de minim 7 zile înainte de eficient la doze terapeutice tratamentul antifungic. 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.

Shingrix Avrupa Birliği - Romence - EMA (European Medicines Agency)

shingrix

glaxosmithkline biologicals sa - recombinant varicella zoster virus glycoprotein e - herpes zoster - vaccinuri - shingrix is indicated for prevention of herpes zoster (hz) and post-herpetic neuralgia (phn), in:adults 50 years of age or older;adults 18 years of age or older at increased risk of hz. utilizarea de shingrix ar trebui să fie în conformitate cu recomandările oficiale.

Rispoval IBR Marker + BRSV + PI3 Vivum Romanya - Romence - ICBMV (Institutul pentru Controlul Produselor Biologice si Medicamentelor de Uz Veterinar)

rispoval ibr marker + brsv + pi3 vivum

pfizer animal health ma eeig, marea britanie - virus herpes bovin de tip 1 (bhv-1) - tulpina difivac (virus ibr marker, ge-negativ), vbrs - tulpina 375, v pi3 - tulpina abbott - liofilizat şi solvent pentru suspensie injectabilă - produse biologice - bovine - bovine pentru imunizarea activă a bovinelor, cu vârste mai mari de 2 săptămâni, pentru reducerea simptomelor respiratorii clinice cauzate de bhv1, ibr, pi3.