Europos Sąjunga -
lietuvių -
EMA (European Medicines Agency)
zenalpha
vetcare oy - medetomidine hydrochloride, vatinoxan hydrochloride - psichopatologija, hipnotizai ir raminamieji preparatai - Šunys - to provide restraint, sedation and analgesia during conduct of non-invasive, non-painful or mildly painful procedures and examinations intended to last no more than 30 minutes.
Europos Sąjunga -
lietuvių -
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) - limfoma, mantle-cell - antinavikiniai vaistai - 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).
Europos Sąjunga -
lietuvių -
EMA (European Medicines Agency)
crysvita
kyowa kirin holdings b.v. - burosumab - hypophosphatemia, familial; hypophosphatemic rickets, x-linked dominant; osteomalacia - narkotikai kaulų ligų gydymui - crysvita is indicated for the treatment of x-linked hypophosphataemia, in children and adolescents aged 1 to 17 years with radiographic evidence of bone disease, and in adults. crysvita is indicated for the treatment of fgf23-related hypophosphataemia in tumour-induced osteomalacia associated with phosphaturic mesenchymal tumours that cannot be curatively resected or localised in children and adolescents aged 1 to 17 years and in adults.
Lietuva -
lietuvių -
SMCA (Valstybinė vaistų kontrolės tarnyba)
velgyn
exeltis baltics, uab - etinilestradiolis/drospirenonas - plėvele dengtos tabletės - 0,02 mg/3 mg - drospirenone and ethinylestradiol
Europos Sąjunga -
lietuvių -
EMA (European Medicines Agency)
evoltra
sanofi b.v. - klofarabinas - prekursorių ląstelių limfoblastinė leukemija-limfoma - antinavikiniai vaistai - Ūmus limfoblastine leukemija (Ūll) pediatrijos pacientams, kuriems buvo recidyvas ar gavus ne mažiau kaip dviejų ankstesnių režimai yra ugniai atsparių gydymui ir tais atvejais, kai nėra jokių kitų gydymo būdas tikimasi sukelti tvirtas atsakas. saugumas ir veiksmingumas buvo įvertintas atliekant tyrimus pacientai ≤ 21 metų amžiaus trisdešimtaisiais.
Europos Sąjunga -
lietuvių -
EMA (European Medicines Agency)
xeplion
janssen-cilag international n.v. - paliperidono palmitatas - Šizofrenija - psicholeptikai - xeplion skiriamas palaikomąjį gydymą šizofrenija sergantiems suaugusiesiems, stabilizuota paliperidonu arba risperidonu. in selected adult patients with schizophrenia and previous responsiveness to oral paliperidone or risperidone, xeplion may be used without prior stabilisation with oral treatment if psychotic symptoms are mild to moderate and a long-acting injectable treatment is needed.