Eiropas Savienība - latviešu - EMA (European Medicines Agency)

shionogi b.v. - lusutrombopag - trombocitopēnija - antihemorāģija - mulpleo ir indicēts, lai ārstētu smaga trombocitopēnija pieaugušiem pacientiem ar hronisku aknu slimību pārcieš invazīvās procedūras,.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

swedish orphan biovitrum ab (publ) - avatrombopag maleate - trombocitopēnija - antihemorāģija - doptelet ir indicēts, lai ārstētu smaga trombocitopēnija pieaugušiem pacientiem ar hronisku aknu slimību, kas ir plānots veikt invazīvo procedūru. doptelet is indicated for the treatment of primary chronic immune thrombocytopenia (itp) in adult patients who are refractory to other treatments (e. kortikosteroīdi, imūnglobulīni).

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

novartis europharm limited - eltrombopags - purpura, trombocitopēnija, idiopātija - other systemic hemostatics, antihemorrhagics - revolade is indicated for the treatment of adult patients with primary immune thrombocytopenia (itp) who are refractory to other treatments (e. corticosteroids, immunoglobulins) (see sections 4. 2 un 5. revolade is indicated for the treatment of paediatric patients aged 1 year and above with primary immune thrombocytopenia (itp) lasting 6 months or longer from diagnosis and who are refractory to other treatments (e. corticosteroids, immunoglobulins) (see sections 4. 2 un 5. revolade is indicated in adult patients with chronic hepatitis c virus (hcv) infection for the treatment of thrombocytopenia, where the degree of thrombocytopenia is the main factor preventing the initiation or limiting the ability to maintain optimal interferon-based therapy (see sections 4. 4 and 5. revolade is indicated in adult patients with acquired severe aplastic anaemia (saa) who were either refractory to prior immunosuppressive therapy or heavily pretreated and are unsuitable for haematopoietic stem cell transplantation (see section 5.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

instituto grifols s.a. - fostamatinib dinātrija - trombocitopēnija - citi hemostatiskie līdzekļi sistēmiskai lietošanai - tavlesse ir indicēts, lai ārstētu hronisku trombocitopēnija imūnās (ipp) pieaugušiem pacientiem, kam ir grūti kūstoši uz citām zālēm.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

amgen europe b.v. - romiplostim - purpura, trombocitopēnija, idiopātija - antihemorāģija - adults:nplate is indicated for the treatment of primary immune thrombocytopenia  (itp) in adult patients who are refractory to other treatments (e. kortikosteroīdi, imūnglobulīni). paediatrics:nplate is indicated for the treatment of chronic primary immune thrombocytopenia (itp) in paediatric patients one year of age and older who are refractory to other treatments (e. kortikosteroīdi, imūnglobulīni).

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

novartis europharm limited - asciminib hydrochloride - leikēmija, mielogēns, hronisks, bcr-abl pozitīvs - antineoplastiski līdzekļi - 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.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

bayer ag - rivaroxaban - arthroplasty, replacement; venous thromboembolism - antitrombotiskie līdzekļi - xarelto, co-ievadīts ar acetilsalicilskābi (asa) atsevišķi vai kopā ar asa plus klopidogrelu vai ticlopidine, ir norādīts, lai novērstu atherothrombotic notikumiem pieaugušiem pacientiem pēc akūta koronāra sindroma (acs) ar paaugstinātu sirds izmeklējumus. xarelto, co-administered with acetylsalicylic acid (asa), is indicated for the prevention of atherothrombotic events in adult patients with coronary artery disease (cad) or symptomatic peripheral artery disease (pad) at high risk of ischaemic events. venozās trombembolijas (vte) profilakse pieaugušiem pacientiem, kuriem tiek veikta gēnu vai ceļa locītavas locītavas operācija. Ārstēšana ar dziļo vēnu tromboze (dvt) un plaušu embolija (pe), un novērst atkārtotu dvt un pe pieaugušajiem. adultsprevention of stroke and systemic embolism in adult patients with non-valvular atrial fibrillation with one or more risk factors, such as congestive heart failure, hypertension, age ≥ 75 years, diabetes mellitus, prior stroke or transient ischaemic attack. paediatric population treatment of venous thromboembolism (vte) and prevention of vte recurrence in children and adolescents aged less than 18 years and weighing from 30 kg to 50 kg after at least 5 days of initial parenteral anticoagulation treatment. paediatric population treatment of venous thromboembolism (vte) and prevention of vte recurrence in children and adolescents aged less than 18 years and weighing more than 50 kg after at least 5 days of initial parenteral anticoagulation treatment.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

takeda pharma a/s - iksazomib citrāts - multiple mieloma - antineoplastiski līdzekļi - ninlaro kombinācijā ar lenalidomīdu un deksametazonu ir paredzēts pieaugušo pacientu ar multiplo mielomu ārstēšanai, kuri saņēmuši vismaz vienu iepriekšēju terapiju.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

glaxosmithkline (ireland) limited - belantamab mafodotin - multiple mieloma - antineoplastiski līdzekļi - blenrep is indicated as monotherapy for the treatment of multiple myeloma in adult patients, who have received at least four prior therapies and whose disease is refractory to at least one proteasome inhibitor, one immunomodulatory agent, and an anti-cd38 monoclonal antibody, and who have demonstrated disease progression on the last therapy.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

novartis europharm limited - ruksolitinibs (fosfāts) - myeloproliferative disorders; polycythemia vera; graft vs host disease - antineoplastiski līdzekļi - myelofibrosis (mf)jakavi is indicated for the treatment of disease related splenomegaly or symptoms in adult patients with primary myelofibrosis (also known as chronic idiopathic myelofibrosis), post polycythaemia vera myelofibrosis or post essential thrombocythaemia myelofibrosis. polycythaemia vera (pv)jakavi ir norādīts ārstēšanai pieaugušiem pacientiem ar polycythaemia vera, kas ir izturīgas pret vai nepanes hydroxyurea. graft versus host disease (gvhd)jakavi is indicated for the treatment of patients aged 12 years and older with acute graft versus host disease or chronic graft versus host disease who have inadequate response to corticosteroids or other systemic therapies (see section 5.