Euroopa Liit - eesti - EMA (European Medicines Agency)

merck sharp & dohme b.v. - caspofungin (as acetate) - candidiasis; aspergillosis - antimükoosid süsteemseks kasutamiseks - treatment of invasive candidiasis in adult or paediatric patients;treatment of invasive aspergillosis in adult or paediatric patients who are refractory to or intolerant of amphotericin b, lipid formulations of amphotericin b and / or itraconazole. refractoriness is defined as progression of infection or failure to improve after a minimum of seven days of prior therapeutic doses of effective antifungal therapy;empirical therapy for presumed fungal infections (such as candida or aspergillus) in febrile, neutropaenic adult or paediatric patients.

Euroopa Liit - eesti - EMA (European Medicines Agency)

chanelle pharmaceuticals manufacturing limited - sevofluraan - valuvaigistid, üldine - dogs; cats - anesteesia indutseerimiseks ja säilitamiseks.

Euroopa Liit - eesti - EMA (European Medicines Agency)

les laboratoires servier - irinotecan anhydrous free-base - pankrease neoplasmid - antineoplastilised ained - metastaatilise ravi, koos 5-fluorouratsiili (5-fu) ja leukovoriiniga (lv), täiskasvanud patsientidel, kelle haigus pärast gemtsitabiini ravi põhineb ravi.

Euroopa Liit - eesti - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - afoxolaner - ektoparasiitsiidid süsteemseks kasutamiseks - koerad - ravi kirbu (ctenocephalides felis ja c.. canis) infestatsioonid. seda toodet saab kasutada kirbuallergia dermatiidi (fad) ravistrateegia osana.. ravi rist (dermacentor reticulatus, ixodes ricinus, rhipicephalus sanguineus) infestatsioonid. ravi demodicosis (põhjustatud demodex canis). ravi sarcoptic mange (põhjustatud sarcoptes scabiei var. canis).

Eesti - eesti - Ravimiamet

takeda pharma as - fenoksümetüülpenitsilliin - õhukese polümeerikattega tablett - 1000000rÜ 10tk; 1000000rÜ 20tk; 1000000rÜ 30tk; 1000000rÜ 100tk

Eesti - eesti - Ravimiamet

grindeks as - broomheksiin - siirup - 0,8mg 1ml 100ml 1tk

Euroopa Liit - eesti - EMA (European Medicines Agency)

sanofi winthrop industrie - dupilumab - dermatitis, atopic; prurigo; esophageal diseases; asthma; sinusitis - dermatiidi ained, välja arvatud kortikosteroidid - atopic dermatitisadults and adolescentsdupixent is indicated for the treatment of moderate-to-severe atopic dermatitis in adults and adolescents 12 years and older who are candidates for systemic therapy. children 6 months to 11 years of agedupixent is indicated for the treatment of severe atopic dermatitis in children 6 months to 11 years old who are candidates for systemic therapy. asthmaadults and adolescentsdupixent is indicated in adults and adolescents 12 years and older as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils and/or raised fraction of exhaled nitric oxide (feno), see section 5. 1, who are inadequately controlled with high dose inhaled corticosteroids (ics) plus another medicinal product for maintenance treatment. children 6 to 11 years of agedupixent is indicated in children 6 to 11 years old as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils and/or raised fraction of exhaled nitric oxide (feno), who are inadequately controlled with medium to high dose inhaled corticosteroids (ics) plus another medicinal product for maintenance treatment. chronic rhinosinusitis with nasal polyposis (crswnp)dupixent is indicated as an add-on therapy with intranasal corticosteroids for the treatment of adults with severe crswnp for whom therapy with systemic corticosteroids and/or surgery do not provide adequate disease control. prurigo nodularis (pn)dupixent is indicated for the treatment of adults with moderate-to-severe prurigo nodularis (pn) who are candidates for systemic therapy. eosinophilic esophagitis (eoe)dupixent is indicated for the treatment of eosinophilic esophagitis in adults and adolescents 12 years and older, weighing at least 40 kg, who are inadequately controlled by, are intolerant to, or who are not candidates for conventional medicinal therapy.

Eesti - eesti - Ravimiamet

dne pharma as - levometadoon - suukaudne lahus üheannuselises konteineris - 75mg 7tk; 75mg 1tk

Eesti - eesti - Ravimiamet

dne pharma as - levometadoon - suukaudne lahus üheannuselises konteineris - 55mg 7tk; 55mg 1tk

Eesti - eesti - Ravimiamet

dne pharma as - levometadoon - suukaudne lahus üheannuselises konteineris - 60mg 7tk