DEXAMETHASON KRKA tablett Eesti - eesti - Ravimiamet

dexamethason krka tablett

first pharma oÜ - deksametasoon - tablett - 20mg 60tk; 20mg 20tk; 20mg 30tk; 20mg 50tk; 20mg 10tk; 20mg 100tk

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

reblozyl

bristol myers squibb pharma eeig - luspatercept - anemia; myelodysplastic syndromes; beta-thalassemia - muud antianemic preparaadid - reblozyl is indicated for the treatment of adult patients with transfusion-dependent anaemia due to very low, low and intermediate-risk myelodysplastic syndromes (mds) with ring sideroblasts, who had an unsatisfactory response to or are ineligible for erythropoietin-based therapy (see section 5. reblozyl is indicated in adults for the treatment of anaemia associated with transfusion dependent and non transfusion dependent beta thalassaemia (see section 5.

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

onureg

bristol-myers squibb pharma eeig - asatsitidiin - leukeemia, müeloidne, äge - antineoplastilised ained - onureg is indicated as maintenance therapy in adult patients with acute myeloid leukaemia (aml) who achieved complete remission (cr) or complete remission with incomplete blood count recovery (cri) following induction therapy with or without consolidation treatment and who are not candidates for, including those who choose not to proceed to, hematopoietic stem cell transplantation (hsct).

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

vidaza

bristol-myers squibb pharma eeig - asatsitidiin - myelodysplastic syndromes; leukemia, myelomonocytic, chronic; leukemia, myeloid, acute - antineoplastilised ained - vidaza is indicated for the treatment of adult patients who are not eligible for haematopoietic stem cell transplantation (hsct) with: intermediate 2 and high-risk myelodysplastic syndromes (mds) according to the international prognostic scoring system (ipss),chronic myelomonocytic leukaemia (cmml) with 10 29 % marrow blasts without myeloproliferative disorder,acute myeloid leukaemia (aml) with 20 30 % blasts and multi-lineage dysplasia, according to world health organisation (who) classification. vidaza is indicated for the treatment of adult patients aged 65 years or older who are not eligible for hsct with aml with >30% marrow blasts according to the who classification.

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

zynteglo

bluebird bio (netherlands) b.v. - autoloogse cd34+ rakkude rikastatud elanikkonnast, mis sisaldab vereloome tüvirakkude transduced koos lentiglobin bb305 lentiviral vektori kodeerimine beeta-a-t87q-globiini geeni - beeta-talasseemia - other hematological agents - zynteglo on näidustatud patsientide raviks 12 aastat ja vanemad koos vereülekande-sõltuv β thalassaemia (tdt), kes ei ole β0/β0 genotüüp, kelle jaoks vereloome tüvirakkude (hsc) siirdamine on asjakohane, kuid inimese leukotsüütide antigeeni (hla)-tasakaalustatud seotud hsc doonor ei ole saadaval.

CONVULEX süste-/infusioonilahus Eesti - eesti - Ravimiamet

convulex süste-/infusioonilahus

g.l. pharma gmbh - valproehape - süste-/infusioonilahus - 100mg 1ml 5ml 5tk

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

vanflyta

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.

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.

ENSTILAR nahavaht Eesti - eesti - Ravimiamet

enstilar nahavaht

leo pharma a/s - kaltsipotriool+beetametasoon - nahavaht - 50mcg+0,5mg 1g 60g 1tk; 50mcg+0,5mg 1g 60g 2tk

VALGANCICLOVIR AUROBINDO õhukese polümeerikattega tablett Eesti - eesti - Ravimiamet

valganciclovir aurobindo õhukese polümeerikattega tablett

aurobindo pharma (malta) limited - valgantsikloviir - õhukese polümeerikattega tablett - 450mg 60tk