Uniunea Europeană - română - EMA (European Medicines Agency)

horizon therapeutics ireland dac - inebilizumab - neuromyelitis optica - imunosupresoare - uplizna is indicated as monotherapy for the treatment of adult patients with neuromyelitis optica spectrum disorders (nmosd) who are anti-aquaporin 4 immunoglobulin g (aqp4-igg) seropositive (see section 5.

Uniunea Europeană - română - EMA (European Medicines Agency)

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) - limfom, mantle-cell - agenți antineoplazici - 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).

Uniunea Europeană - română - EMA (European Medicines Agency)

janssen-cilag international nv - ciltacabtagene autoleucel - mielom multiplu - carvykti is indicated for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least three prior therapies, including an immunomodulatory agent, a proteasome inhibitor and an anti-cd38 antibody and have demonstrated disease progression on the last therapy.

Uniunea Europeană - română - EMA (European Medicines Agency)

neuraxpharm pharmaceuticals s.l. - ublituximab - multiple sclerosis, relapsing-remitting; multiple sclerosis - imunosupresoare - briumvi is indicated for the treatment of adult patients with relapsing forms of multiple sclerosis (rms) with active disease defined by clinical or imaging features.

Uniunea Europeană - română - EMA (European Medicines Agency)

kite pharma eu b.v. - axicabtagene ciloleucel - lymphoma, follicular; lymphoma, large b-cell, diffuse - agenți antineoplazici - 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.

Uniunea Europeană - română - EMA (European Medicines Agency)

novartis ireland ltd - ofatumumab - scleroză multiplă, scleroză multiplă recurent-remisivă - immunosuppressant - kesimpta is indicated for the treatment of adult patients with relapsing forms of multiple sclerosis (rms) with active disease defined by clinical or imaging features (see section 5.

Uniunea Europeană - română - EMA (European Medicines Agency)

boehringer ingelheim international gmbh - telmisartan - hipertensiune - sistemul cardiovascular - tratamentul hipertensiunii arteriale esențiale la adulți:se adauga pe therapyonduarp este indicată la adulți a căror tensiune arterială nu este controlată adecvat cu amlodipină. Înlocuirea therapyadult pacienții tratați cu telmisartan și amlodipină sub formă de comprimate separate pot în schimb să primească tablete de onduarp conțin aceeași componentă doze.

Uniunea Europeană - română - EMA (European Medicines Agency)

medac gesellschaft für klinische spezialpräparate mbh - treosulfan - transplantul de celule stem hematopoietice - agenți antineoplazici - treosulfan in combination with fludarabine is indicated as part of conditioning treatment prior to allogeneic haematopoietic stem cell transplantation (allohsct) in adult patients and in paediatric patients older than one month with malignant and non-malignant diseases.

Uniunea Europeană - română - EMA (European Medicines Agency)

medac gesellschaft fuer klinische spezialpraeparate mbh - asparaginază - leucemia limfoblastică limfoblastică a celulelor precursoare - agenți antineoplazici - spectrila este indicat ca si componenta a antineoplastic combinaţie de terapie pentru tratamentul acut leucemie limfoblastica (toate) la pacienţii pediatrice la nastere la 18 ani şi adulţi.

România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

incdca/magistra c&c srl - romania - diverse - supoz. - 0,5mg - antiinflamatoare intestinale alte antiinflamatoare intestinale