Estonie - estonien - Ravimiamet

laboratoire bioluz - naatriumkloriid - infusioonilahus - 7,2% 3000ml 1tk

Estonie - estonien - Ravimiamet

s.a.l.f. s.p.a. laboratorio farmacologico - naatriumkloriid - infusioonilahus - 72mg 1ml 2000ml 5tk

Estonie - estonien - Ravimiamet

s.a.l.f. s.p.a. laboratorio farmacologico - naatriumkloriid - süste-/infusioonilahus - 9mg 1ml 500ml 12tk; 9mg 1ml 2000ml 5tk; 9mg 1ml 250ml 20tk

Union européenne - estonien - 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.

Union européenne - estonien - 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.

Union européenne - estonien - EMA (European Medicines Agency)

daiichi sankyo europe gmbh - quizartinib dihydrochloride - leukeemia, müeloid - antineoplastic agents, protein kinase inhibitors - vanflyta is indicated in combination with standard cytarabine and anthracycline induction and standard cytarabine consolidation chemotherapy, followed by vanflyta single-agent maintenance therapy for adult patients with newly diagnosed acute myeloid leukaemia (aml) that is flt3-itd positive.

Union européenne - estonien - EMA (European Medicines Agency)

gilead sciences international ltd  - emtricitabine, rilpivirine hydrochloride, tenofovir disoproxil fumarate - hiv-nakkused - viirusevastased ravimid süsteemseks kasutamiseks - eviplera on näidustatud täiskasvanute nakatunud inimese immuunpuudulikkuse viiruse tüüp 1 (hiv-1) ilma teadaolevate resistentsusega seotud mittenukleosiidsed pöördtranskriptaasi inhibiitorite (nnrti) klassi, tenofoviiri või emtritsitabiini, ja koos nakkav laadida ≤ 100 000 hiv-1 rna koopiat/ml. nagu teistegi retroviiruse vastaste ravimite puhul, peaks eviplera kasutamine viitama genotüpilise resistentsustestidele ja / või ajaloolistele resistentsuse andmetele..

Estonie - estonien - Ravimiamet

grindeks as - metformiin+sitagliptiin - õhukese polümeerikattega tablett - 850mg+50mg 98tk; 850mg+50mg 28tk; 850mg+50mg 56tk

Estonie - estonien - Ravimiamet

grindeks as - metformiin+sitagliptiin - õhukese polümeerikattega tablett - 1000mg+50mg 28tk; 1000mg+50mg 56tk; 1000mg+50mg 98tk; 1000mg+50mg 196tk

Union européenne - estonien - EMA (European Medicines Agency)

novartis europharm limited - asciminib hydrochloride - leukeemia, müelogeenne, krooniline, bcr-abl positiivne - antineoplastilised ained - scemblix is indicated for the treatment of adult patients with philadelphia chromosome positive chronic myeloid leukaemia in chronic phase (ph+ cml cp) previously treated with two or more tyrosine kinase inhibitors (see section 5.