POLYGYNAX vaginaalpehmekapsel Eesti - eesti - Ravimiamet

polygynax vaginaalpehmekapsel

innothera chouzy - nüstatiin+neomütsiin+polümüksiin b - vaginaalpehmekapsel - 100000rÜ+35000rÜ+35000rÜ 6tk

IDEOS närimistablett Eesti - eesti - Ravimiamet

ideos närimistablett

laboratoire innotech international - kaltsium+kolekaltsiferool - närimistablett - 500mg+400rÜ 30tk

FLUDITEC siirup Eesti - eesti - Ravimiamet

fluditec siirup

laboratoire innotech international - karbotsüsteiin - siirup - 20mg 1ml 125ml 1tk

PHARMATEX vaginaalsuposiit Eesti - eesti - Ravimiamet

pharmatex vaginaalsuposiit

laboratoire innotech international - bensalkooniumkloriid - vaginaalsuposiit - 18,9mg 10tk

PHARMATEX 12MG/G vaginaalkreem Eesti - eesti - Ravimiamet

pharmatex 12mg/g vaginaalkreem

laboratoire innotech international - bensalkooniumkloriid - vaginaalkreem - 1,2% 72g 1tk

FLUDITEC siirup Eesti - eesti - Ravimiamet

fluditec siirup

laboratoire innotech international - karbotsüsteiin - siirup - 50mg 1ml 125ml 1tk

TOTYLEM õhukese polümeerikattega tablett Eesti - eesti - Ravimiamet

totylem õhukese polümeerikattega tablett

laboratoire innotech international - raud(ii)glükonaat+foolhape - õhukese polümeerikattega tablett - 60mg+0,4mg 30tk

Celvapan Euroopa Liit - eesti - EMA (European Medicines Agency)

celvapan

nanotherapeutics bohumil, s.r.o. - whole virion influenza vaccine, inactivated containing antigen of strain a/california/07/2009 (h1n1)v - disease outbreaks; influenza, human; immunization - vaktsiinid - a (h1n1) v 2009 viirusega põhjustatud gripi profülaktika. celvapan tuleks kasutada vastavalt euroopa liidu arendus.

Dupixent Euroopa Liit - eesti - EMA (European Medicines Agency)

dupixent

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.

Mircera Euroopa Liit - eesti - EMA (European Medicines Agency)

mircera

roche registration gmbh - metoksü polüetüleenglükool-epoetin beta - anemia; kidney failure, chronic - antianemilised preparaadid - treatment of symptomatic anaemia associated with chronic kidney disease (ckd) in adult patients (see section 5. treatment of symptomatic anaemia associated with chronic kidney disease (ckd) in paediatric patients from 3 months to less than 18 years of age who are converting from another erythropoiesis stimulating agent (esa) after their haemoglobin level was stabilised with the previous esa (see section 5.