Viro - viro - Ravimiamet

viatris healthcare limited - aselastiin - ninasprei, lahus - 1,5mg 1ml 20ml 1tk; 1,5mg 1ml 22ml 1tk; 1,5mg 1ml 10ml 1tk; 1,5mg 1ml 17ml 1tk

Viro - viro - Ravimiamet

teva b.v. - dekvaliin+tsinhokaiin - loseng - 0,25mg+0,03mg 40tk; 0,25mg+0,03mg 30tk; 0,25mg+0,03mg 20tk

Viro - viro - Ravimiamet

grindeks as - lidokaiin - süstelahus - 20mg 1ml 5ml 10tk

Viro - viro - Ravimiamet

opella healthcare france s.a.s. - püridoksiin+magneesium - kaetud tablett - 5mg+470mg 60tk; 5mg+470mg 50tk

Euroopan unioni - viro - EMA (European Medicines Agency)

astrazeneca ab - metformiin vesinikkloriid, saxagliptin, dapagliflozin - suhkurtõbi, tüüp 2 - diabeetis kasutatavad ravimid - qtrilmet on näidustatud täiskasvanutel vanuses 18 aastat ja vanemad, tüüp 2 diabeet:parandada glycaemic kontrollida, kui metformiin koos või ilma sulphonylurea (su) ja kas saxagliptin või dapagliflozin ei anna adekvaatset kontrolli glycaemic. kui juba ravitakse metformiin ja saxagliptin ja dapagliflozin.

Euroopan unioni - viro - EMA (European Medicines Agency)

dipharma arzneimittel gmbh - sapropterin dihüdrokloriid - fenüülketonuria - muud alimentary seedetrakti ja ainevahetust tooted, - sapropterin dipharma is indicated for the treatment of hyperphenylalaninaemia (hpa) in adults and paediatric patients of all ages with phenylketonuria (pku) who have been shown to be responsive to such treatment. sapropterin dipharma is also indicated for the treatment of hyperphenylalaninaemia (hpa) in adults and paediatric patients of all ages with tetrahydrobiopterin (bh4) deficiency who have been shown to be responsive to such treatment.

Euroopan unioni - viro - EMA (European Medicines Agency)

genzyme europe bv - sevelamer vesinikkloriid - hyperphosphatemia; renal dialysis - kõik muud ravitoimingud - tasemäär on näidustatud hüperfosfateemia kontrollimiseks täiskasvanud patsientidel, kes saavad hemodialüüsi või peritoneaaldialüüsi. sevelameerhüdrokloriidi võib arvesse võtta kaltsiumilisandeid, mis võib sisaldada kaltsiumilisandeid, 1,25-dihüdroksü vitamiin d3 või ühte selle analoogidest kontrollimiseks tingitud luuhaiguse raviks kasutada.

Euroopan unioni - viro - EMA (European Medicines Agency)

bristol myers squibb pharma eeig - fedratinib dihydrochloride monohydrate - myeloproliferative disorders; primary myelofibrosis - antineoplastilised ained - inrebic is indicated for the treatment of disease-related splenomegaly or symptoms in adult patients with primary myelofibrosis, post polycythaemia vera myelofibrosis or post essential thrombocythaemia myelofibrosis who are janus associated kinase (jak) inhibitor naïve or have been treated with ruxolitinib.

Euroopan unioni - viro - EMA (European Medicines Agency)

biocryst ireland limited - berotralstat dihydrochloride - angioödeem, pärilik - other hematological agents - orladeyo is indicated for routine prevention of recurrent attacks of hereditary angioedema (hae) in adult and adolescent patients aged 12 years and older.

Euroopan unioni - viro - EMA (European Medicines Agency)

novartis europharm limited  - capmatinib dihydrochloride monohydrate - kartsinoom, mitteväikerakk-kopsu - antineoplastilised ained - tabrecta as monotherapy is indicated for the treatment of adult patients with advanced non small cell lung cancer (nsclc) harbouring alterations leading to mesenchymal epithelial transition factor gene exon 14 (metex14) skipping, who require systemic therapy following prior treatment with immunotherapy and/or platinum based chemotherapy.