Den europeiske union - estisk - EMA (European Medicines Agency)

sfl pharmaceuticals deutschland gmbh - nyxthracis - anthrax - suguhormoonid ja immunoglobuliinid, - obiltoxaximab sfl is indicated in combination with appropriate antibacterial drugs in all age groups for treatment of inhalational anthrax due to bacillus anthracis (see section 5. obiltoxaximab sfl is indicated in all age groups for post-exposure prophylaxis of inhalational anthrax when alternative therapies are not appropriate or are not available (see section 5.

Den europeiske union - estisk - EMA (European Medicines Agency)

pfizer europe ma eeig - pneumococcal polysaccharide serotype 1, pneumococcal polysaccharide serotype 3, pneumococcal polysaccharide serotype 4, pneumococcal polysaccharide serotype 5, pneumococcal polysaccharide serotype 6a, pneumococcal polysaccharide serotype 6b, pneumococcal polysaccharide serotype 7f, pneumococcal polysaccharide serotype 8, pneumococcal polysaccharide serotype 9v, pneumococcal polysaccharide serotype 10a, pneumococcal polysaccharide serotype 11a, pneumococcal polysaccharide serotype 12f, pneumococcal polysaccharide serotype 14, pneumococcal polysaccharide serotype 15b, pneumococcal polysaccharide serotype 18c, pneumococcal polysaccharide serotype 19a, pneumococcal polysaccharide serotype 19f, pneumococcal polysaccharide serotype 22f, pneumococcal polysaccharide serotype 23f, pneumococcal polysaccharide serotype 33f - pneumokoki infektsioonid - vaktsiinid - active immunisation for the prevention of invasive disease and pneumonia caused by streptococcus pneumoniae in individuals 18 years of age and older. vt lõigud 4. 4 ja 5. 1, mis käsitleb kaitset spetsiifiliste pneumokokkide serotüüpide eest. apexxnar should be used in accordance with official recommendations. .

Den europeiske union - estisk - EMA (European Medicines Agency)

merck sharp & dohme b.v.  - pneumococcal polysaccharide conjugate vaccine (adsorbed) - pneumokoki infektsioonid - pneumococcus, purified polysaccharides antigen conjugated - vaxneuvance is indicated for active immunisation for the prevention of invasive disease, pneumonia and acute otitis media caused by streptococcus pneumoniae in infants, children and adolescents from 6 weeks to less than 18 years of age. vaxneuvance is indicated for active immunisation for the prevention of invasive disease and pneumonia caused by streptococcus pneumoniae in individuals 18 years of age and older. vt lõigud 4. 4 ja 5. 1, mis käsitleb kaitset spetsiifiliste pneumokokkide serotüüpide eest. the use of vaxneuvance should be in accordance with official recommendations.

Den europeiske union - estisk - EMA (European Medicines Agency)

takeda pharma a/s - azilsartan medoxomil - hüpertensioon - reniini-angiotensiini süsteemi toimivad ained - ipreziv on näidustatud essentsiaalse hüpertensiooni raviks täiskasvanutel.

Estland - estisk - Ravimiamet

fresenius medical care deutschland gmbh - naatriumkloriid+kaaliumkloriid+kaltsiumkloriiddihüdraat+magneesiumkloriid+glükoos+naatriumvesinikkarbonaat - hemodialüüsi-/hemofiltratsioonilahus - 6,048g+0,1491g+0,2205g+0,1016g+1,1g+3,066g 1l 5000ml 2tk

Estland - estisk - Ravimiamet

fresenius medical care deutschland gmbh - naatriumkloriid+kaltsiumkloriiddihüdraat+magneesiumkloriid+glükoos+naatriumvesinikkarbonaat - hemodialüüsi-/hemofiltratsioonilahus - 6,048g+0,2205g+0,1016g+1,1g+3,066g 1l 5000ml 2tk

Estland - estisk - Ravimiamet

strides arcolab international limited - gemtsitabiin - infusioonilahuse pulber - 38mg 1ml 200mg 1tk; 38mg 1ml 1000mg 1tk

Estland - estisk - Ravimiamet

fresenius medical care deutschland gmbh - naatriumkloriid+kaaliumkloriid+kaltsiumkloriiddihüdraat+magneesiumkloriid+glükoos+naatriumvesinikkarbonaat - hemodialüüsi-/hemofiltratsioonilahus - 6,048g+0,298g+0,2205g+0,1016g+1,1g+3,066g 1l 5000ml 2tk

Estland - estisk - Ravimiamet

fresenius medical care deutschland gmbh - naatriumkloriid+kaaliumkloriid+kaltsiumkloriiddihüdraat+magneesiumkloriid+glükoos+naatriumvesinikkarbonaat - hemodialüüsi-/hemofiltratsioonilahus - 6,048g+0,224g+0,2205g+0,1016g+1,1g+3,066g 1l 5000ml 2tk

Den europeiske union - estisk - EMA (European Medicines Agency)

siga technologies netherlands b.v. - tecovirimat - poxviridae infections; cowpox; monkeypox; vaccinia; smallpox - viirusevastased ravimid süsteemseks kasutamiseks - tecovirimat siga is indicated for the treatment of the following viral infections in adults and children with body weight at least 13 kg:- smallpox- monkeypox- cowpoxtecovirimat siga is also indicated to treat complications due to replication of vaccinia virus following vaccination against smallpox in adults and children with body weight at least 13 kg (see sections 4. 4 ja 5. tecovirimat siga should be used in accordance with official recommendations.