Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

devatis ag - posaconazolum - sospensione orale - posaconazolum 200 mg, polysorbatum 80, xanthani gummi, natrii benzoas 10 mg, acidum citricum monohydricum, natrii citras dihydricus, glycerolum, glucosum liquidum 1750 mg, e 171, simeticonum, polysorbatum 65, methylcellulosum, macrogoli stearas, mono/diglycerida, e 200, e 210 0.045 mg, acidum sulfuricum, aromatica (kirschen) cum propylenglycolum 14.35 mg, aqua purificata ad suspensionem pro 5 ml corresp. natrium 3.4 mg. - infezioni fungine - synthetika

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

viatris pharma gmbh - posaconazolum - sospensione orale - posaconazolum 200 mg, acidum citricum monohydricum, natrii dihydrogenocitras anhydricus, natrii benzoas 10 mg, natrii laurilsulfas, simeticonum, methylcellulosum, acidum sorbicum, xanthani gummi, glycerolum, glucosum liquidum 2108.5 mg, e 171, aromatica (kirschen), aqua purificata ad suspensionem pro 5 ml corresp. natrium 5.91 mg. - infezioni fungine - synthetika

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

viatris pharma gmbh - posaconazolum - compressa gastroresistente - posaconazolum 100 mg, acidi methacrylici et ethylis acrylatis polymerisatum 1:1, triethylis citras, xylitolum, hydroxypropylcellulosum, e 310, cellulosum microcristallinum, silica colloidalis anhydrica, carmellosum natricum conexum, natrii stearylis fumaras, Überzug: poly(alcohol vinylicus), e 171, macrogolum 3350, talcum, e 172 (flavum), pro compresso obducto corresp. natrium 2.4 mg. - infezioni fungine - synthetika

Unione Europea - italiano - EMA (European Medicines Agency)

pfizer europe ma eeig - nirmatrelvir, ritonavir - covid-19 virus infection - paxlovid is indicated for the treatment of coronavirus disease 2019 (covid-19) in adults who do not require supplemental oxygen and who are at increased risk for progressing to severe covid 19.

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

fosun pharma sp zoo -

Unione Europea - italiano - EMA (European Medicines Agency)

merck sharp and dohme b.v - posaconazolo - candidiasis; mycoses; coccidioidomycosis; aspergillosis - antimicotici per uso sistemico - noxafil gastro-resistant tablets are indicated for use in the treatment of the following fungal infections in adults (see sections 4. 2 e 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 e 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. la refrattarietà è definito come la progressione di infezione o di mancata migliorare dopo un minimo di 7 giorni prima di dosi terapeutiche di una efficace terapia antimicotica. 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 e 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 e 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 e 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. la refrattarietà è definito come la progressione di infezione o di mancata migliorare dopo un minimo di 7 giorni prima di dosi terapeutiche di una efficace terapia antimicotica. 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 e 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 e 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. la refrattarietà è definito come la progressione di infezione o di mancata migliorare dopo un minimo di 7 giorni prima di dosi terapeutiche di una efficace terapia antimicotica. 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):- aspergillosi invasiva in pazienti con malattia refrattaria ad amfotericina b o ad itraconazolo o in pazienti intolleranti a questi farmaci;- fusariosi in pazienti con malattia refrattaria ad amfotericina b o in pazienti che sono intolleranti di amfotericina b;- chromoblastomycosis e mycetoma in pazienti con malattia refrattaria ad itraconazolo o in pazienti che sono intolleranti di itraconazolo;- coccidioidomicosi in pazienti con malattia refrattaria ad amfotericina b, itraconazolo o fluconazolo o in pazienti intolleranti a questi farmaci;- candidiasi orofaringea: come terapia di prima linea in pazienti che hanno grave malattia o immunocompromessi, in cui la risposta alla terapia attuale è previsto per essere poveri. la refrattarietà è definito come la progressione di infezione o di mancata migliorare dopo un minimo di 7 giorni prima di dosi terapeutiche di una efficace terapia antimicotica. 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.

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

pfizer ag - fluconazolum - soluzione per infusione - fluconazolum 2 mg, natrii chloridum, aqua ad iniectabile q.s. ad solutionem pro 1 ml. - antifungini - synthetika

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

abbvie ag - ritonavirum - sirup - ritonavirum 600 mg, aromatica, saccharinum natricum, color.: e 110, excipiens ad solutionem pro 7.5 ml corresp. ethanolum 43.2 % v/v. - hiv-infektionen - synthetika human

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

abbvie ag - lopinavirum, ritonavirum - sirup - lopinavirum 80 mg, ritonavirum 20 mg, macrogolglyceroli hydroxystearas 10.2 mg, aqua purificata, natrii chloridum, natrii citras dihydricus, saccharinum natricum, acesulfamum kalicum, acidum citricum, ethanolum anhydricum 356.3 mg, propylenglycolum 152.7 mg, levomentholum, povidonum k 29-32, glycerolum, sirupus saccharidae corresp. fructosum 101.2 mg et glucosum 59.1 mg, ammonii glycyrrhizas, menthae piperitae aetheroleum, aromatica (vanille) cum glucosum et natrii benzoas, aromatica (zuckerwatte), ad solutionem pro 1 ml corresp. ethanolum 42.4 % v/v et natrium 2.41 mg. - le infezioni da hiv - synthetika

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

pfizer ag - voriconazolum - polvere per concentrato per soluzione per infusione - voriconazolum 0.2 g, sulfobutylbetadexum natricum 3.2 g, pro vitro corresp. natrium 0.221 g. - infezioni fungine - synthetika