Europska Unija - hrvatski - EMA (European Medicines Agency)

angelini pharma s.p.a - cenobamate - epilepsija - antiepileptici sredstva, - 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.

Europska Unija - hrvatski - EMA (European Medicines Agency)

glaxo group limited  - retigabinje - epilepsija - antiepileptici sredstva, - trobalt je indiciran kao adjuvantna terapija otporna djelomično pojavu napadaja sa ili bez sekundarne generalizacije u bolesnika u dobi od 18 godina ili stariji od epilepsije, gdje druge odgovarajuće droge kombinacije pokazale neprikladnima ili nisu podnosi.

Europska Unija - hrvatski - EMA (European Medicines Agency)

eisai gmbh - perampanel - epilepsije, djelomično - antiepileptici sredstva, drugi antiepileptici sredstva - fycompa je indicirana adjuvantna liječenje parcijalnih napadaja sa ili bez sekundarno generaliziranih napadaja u odraslih i adolescenata od 12 godina s epilepsijom. fycompa indiciran za dodatna terapija u početku генерализованных тонико-клонические napadaja kod odraslih i adolescenata bolesnika 12 godina s idiopatskom epilepsijom postati generalizirani.

Europska Unija - hrvatski - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - idecabtagene vicleucel - multiple myeloma; neoplasms; cancer; neoplasms, plasma cell; hemostatic disorders; vascular diseases; cardiovascular diseases; paraproteinemias; blood protein disorders; hematologic diseases; hemic and lymphatic diseases; hemorrhagic disorders; infectious mononucleosis; lymphoproliferative disorders; immunoproliferative disorders; immune system diseases - antineoplastična sredstva - abecma 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.

Europska Unija - hrvatski - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - cd19-directed genetically modified autologous cell-based product consisting of purified cd8+ t-cells (cd8+ cells), cd19-directed genetically modified autologous cell-based product consisting of purified cd4+ t cells (cd4+ cells) - lymphoma, large b-cell, diffuse; lymphoma, follicular; mediastinal neoplasms - antineoplastična sredstva - breyanzi is indicated for the treatment of adult patients with diffuse large b-cell lymphoma (dlbcl), high grade b-cell lymphoma (hgbcl), primary mediastinal large b-cell lymphoma (pmbcl) and follicular lymphoma grade 3b (fl3b), who relapsed within 12 months from completion of, or are refractory to, first-line chemoimmunotherapy.

Europska Unija - hrvatski - EMA (European Medicines Agency)

abbvie deutschland gmbh & co. kg - epcoritamab - lymphoma, large b-cell, diffuse - antineoplastična sredstva - tepkinly as monotherapy is indicated for the treatment of adult patients with relapsed or refractory diffuse large b-cell lymphoma (dlbcl) after two or more lines of systemic therapy.

Europska Unija - hrvatski - EMA (European Medicines Agency)

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

Europska Unija - hrvatski - 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, mantel-stanica - antineoplastična sredstva - 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).

Europska Unija - hrvatski - EMA (European Medicines Agency)

mitsubishi pharma europe ltd - colestilan - hiperfosfatemija - lijekovi za liječenje hiperkalemije i hiperfosfatemije - liječenje hiperfosfatemije u odraslih bolesnika s kroničnom bolesti bubrega, stupanj 5, koji primaju hemodijalizu ili peritonealnu dijalizu.

Europska Unija - hrvatski - EMA (European Medicines Agency)

bial - portela & ca, s.a. - eslikarbazepin acetat - epilepsija - antiepileptici sredstva, - zebinix je indiciran kao pomoćna terapija kod odraslih, adolescenata i djece iznad 6 godina, s parcijalnim napadajima sa ili bez sekundarne generalizacije.