Zinbryta 欧州連合 - エストニア語 - EMA (European Medicines Agency)

zinbryta

biogen idec ltd - daklüsumab - hulgiskleroos - immunosupressandid - zinbryta on näidustatud täiskasvanud patsientidel hulgiskleroosi retsidiivsete vormide (rms).

Yescarta 欧州連合 - エストニア語 - EMA (European Medicines Agency)

yescarta

kite pharma eu b.v. - axicabtagene ciloleucel - lymphoma, follicular; lymphoma, large b-cell, diffuse - antineoplastilised ained - yescarta is indicated for the treatment of adult patients with diffuse large b cell lymphoma (dlbcl) and high-grade b-cell lymphoma (hgbl) that relapses within 12 months from completion of, or is refractory to, first-line chemoimmunotherapy. yescarta is indicated for the treatment of adult patients with relapsed or refractory (r/r) dlbcl and primary mediastinal large b cell lymphoma (pmbcl), after two or more lines of systemic therapy. yescarta is indicated for the treatment of adult patients with r/r follicular lymphoma (fl) after three or more lines of systemic therapy.

Zynteglo 欧州連合 - エストニア語 - 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.

Spravato 欧州連合 - エストニア語 - EMA (European Medicines Agency)

spravato

janssen-cilag international nv - esketamine vesinikkloriid - depressiivne häire - teised antidepressandid - spravato, koos ssri või snri, on näidustatud täiskasvanute raviks ravimresistentse depressiooniga, kes ei ole vastanud vähemalt kaks erinevat ravi koos antidepressantidega praeguse mõõduka kuni raske depressiivne episood.

Tecartus 欧州連合 - エストニア語 - EMA (European Medicines Agency)

tecartus

kite pharma eu b.v. - autologous peripheral blood t cells cd4 and cd8 selected and cd3 and cd28 activated transduced with retroviral vector expressing anti-cd19 cd28/cd3-zeta chimeric antigen receptor and cultured (brexucabtagene autoleucel) - lümfoom, mantle-cell - antineoplastilised ained - mantle cell lymphomatecartus is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (mcl) after two or more lines of systemic therapy including a bruton’s tyrosine kinase (btk) inhibitor. acute lymphoblastic leukaemiatecartus is indicated for the treatment of adult patients 26 years of age and above with relapsed or refractory b-cell precursor acute lymphoblastic leukaemia (all).

Skysona 欧州連合 - エストニア語 - EMA (European Medicines Agency)

skysona

bluebird bio (netherlands) b.v. - elivaldogene autotemcel - adrenoleukodystrophy - muud närvisüsteemi ravimid - treatment of early cerebral adrenoleukodystrophy in patients less than 18 years of age, with an abcd1 genetic mutation, and for whom a human leukocyte antigen (hla) matched sibling haematopoietic stem cell donor is not available.

Bimzelx 欧州連合 - エストニア語 - EMA (European Medicines Agency)

bimzelx

ucb pharma s.a.   - bimekizumab - psoriaas - immunosupressandid - plaque psoriasisbimzelx is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. psoriatic arthritisbimzelx, alone or in combination with methotrexate, is indicated for the treatment of active psoriatic arthritis in adults who have had an inadequate response or who have been intolerant to one or more disease-modifying antirheumatic drugs (dmards). axial spondyloarthritisnon-radiographic axial spondyloarthritis (nr-axspa)bimzelx is indicated for the treatment of adults with active non-radiographic axial spondyloarthritis with objective signs of inflammation as indicated by elevated c-reactive protein (crp) and/or magnetic resonance imaging (mri) who have responded inadequately or are intolerant to non-steroidal anti-inflammatory drugs (nsaids). ankylosing spondylitis (as, radiographic axial spondyloarthritis)bimzelx is indicated for the treatment of adults with active ankylosing spondylitis who have responded inadequately or are intolerant to conventional therapy.

Upstaza 欧州連合 - エストニア語 - EMA (European Medicines Agency)

upstaza

ptc therapeutics international limited - eladocagene exuparvovec - aminohapete ainevahetus, kaasasündinud vead - enzymes, other alimentary tract and metabolism products - upstaza is indicated for the treatment of patients aged 18 months and older with a clinical, molecular, and genetically confirmed diagnosis of aromatic l amino acid decarboxylase (aadc) deficiency with a severe phenotype (see section 5.

Hemgenix 欧州連合 - エストニア語 - EMA (European Medicines Agency)

hemgenix

csl behring gmbh - etranacogene dezaparvovec - hemofiilia b - other hematological agents - treatment of severe and moderately severe haemophilia b (congenital factor ix deficiency) in adult patients without a history of factor ix inhibitors.

RHINOCORT ninasprei, suspensioon エストニア - エストニア語 - Ravimiamet

rhinocort ninasprei, suspensioon

mcneil ab - budesoniid - ninasprei, suspensioon - 64mcg 1annus 120annus 1tk