Euroopa Liit - eesti - EMA (European Medicines Agency)

medac gesellschaft für klinische spezialpräparate mbh - arseentrioksiid - leukeemia, promüelotsüütne, äge - antineoplastilised ained - arsenic trioxide medac is indicated for induction of remission, and consolidation in adult patients with:newly diagnosed low-to-intermediate risk acute promyelocytic leukaemia (apl) (white blood cell count, ≤ 10 x 10³/μl) in combination with all-trans-retinoic acid (atra)relapsed/refractory apl (previous treatment should have included a retinoid and chemotherapy) characterised by the presence of the t(15;17) translocation and/or the presence of the pro-myelocytic leukaemia/retinoic-acid-receptor-alpha (pml/rarα) gene. vastuse määr muude ägeda müeloidse leukeemia alatüüpi, et arseentrioksiid ei ole uuritud.

Euroopa Liit - eesti - EMA (European Medicines Agency)

angelini pharma s.p.a - cenobamate - epilepsia - antiepileptics, - adjunctive treatment of focal-onset seizures with or without secondary generalisation in adult patients with epilepsy who have not been adequately controlled despite a history of treatment with at least 2 anti-epileptic medicinal products.

Euroopa Liit - eesti - EMA (European Medicines Agency)

serb sas - glucarpidase - metabolic side effects of drugs and substances - kõik muud ravitoimingud - voraxaze is indicated to reduce toxic plasma methotrexate concentration in adults and children (aged 28 days and older) with delayed methotrexate elimination or at risk of methotrexate toxicity.

Euroopa Liit - eesti - EMA (European Medicines Agency)

pfizer europe ma eeig - somatrogon - growth and development - hÜpofÜÜsi ja hÜpotaalamuse hormoonid ja nende analoogid - indicated for the long-term treatment of paediatric patients with growth disturbance due to insufficient secretion of growth hormone.

Euroopa Liit - eesti - EMA (European Medicines Agency)

laboratorios lesvi s.l. - dimetüülfumaraat - sclerosis multiplex, relapsing-remitting - immunosupressandid - dimethyl fumarate neuraxpharma is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Euroopa Liit - eesti - EMA (European Medicines Agency)

sanofi b.v. - olipudase alfa - acid sphingomyelinase deficiency (asmd) type a/b or type b - muud alimentary seedetrakti ja ainevahetust tooted, - xenpozyme is indicated as an enzyme replacement therapy for the treatment of non-central nervous system (cns) manifestations of acid sphingomyelinase deficiency (asmd) in paediatric and adult patients with type a/b or type b.

Euroopa Liit - eesti - EMA (European Medicines Agency)

roche registration gmbh - mosunetuzumab - lümfoom, follikulaarne - antineoplastic agents, monoclonal antibodies - lunsumio as monotherapy is indicated for the treatment of adult patients with relapsed or refractory follicular lymphoma (fl) who have received at least two prior systemic therapies.

Euroopa Liit - eesti - EMA (European Medicines Agency)

amryt pharmaceuticals dac - octreotide acetate - akromegaalia - hüpofüüsi ja hüpotaalamuse hormoonid ja analoogid - mycapssa is indicated for maintenance treatment in adult patients with acromegaly who have responded to and tolerated treatment with somatostatin analogues.

Euroopa Liit - eesti - EMA (European Medicines Agency)

les laboratoires servier - ivosidenib - leukemia, myeloid, acute; cholangiocarcinoma - antineoplastilised ained - tibsovo in combination with azacitidine is indicated for the treatment of adult patients with newly diagnosed acute myeloid leukaemia (aml) with an isocitrate dehydrogenase-1 (idh1) r132 mutation who are not eligible to receive standard induction chemotherapy (see section 5. tibsovo monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic cholangiocarcinoma with an idh1 r132 mutation who were previously treated by at least one prior line of systemic therapy.

Euroopa Liit - eesti - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - mavacamten - cardiomyopathy, hypertrophic - muud kardiaalsed preparaadid - treatment of symptomatic obstructive hypertrophic cardiomyopathy.