Yescarta यूरोपीय संघ - क्रोएशियाई - EMA (European Medicines Agency)

yescarta

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.

Tecartus यूरोपीय संघ - क्रोएशियाई - 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) - 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).

Libmeldy यूरोपीय संघ - क्रोएशियाई - EMA (European Medicines Agency)

libmeldy

orchard therapeutics (netherlands) bv - atidarsagene autotemcel - leukodystrophy, metachromatic - ostali lijekovi protiv živčanog sustava - libmeldy is indicated for the treatment of metachromatic leukodystrophy (mld) characterized by biallelic mutations in the arysulfatase a (arsa) gene leading to a reduction of the arsa enzymatic activity:in children with late infantile or early juvenile forms, without clinical manifestations of the disease,in children with the early juvenile form, with early clinical manifestations of the disease, who still  have the ability to walk independently and before the onset of cognitive decline.

Abecma यूरोपीय संघ - क्रोएशियाई - EMA (European Medicines Agency)

abecma

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.

Breyanzi यूरोपीय संघ - क्रोएशियाई - EMA (European Medicines Agency)

breyanzi

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.

Zalmoxis यूरोपीय संघ - क्रोएशियाई - EMA (European Medicines Agency)

zalmoxis

molmed spa - alogenih t stanica genetski modificirani sa retrovirusni vektor kodiranje za skraćeni oblik ljudske nizak afinitet receptora faktora rasta živaca (Δlngfr) i herpes simplex virus timidin kinaze (hsv-tk mut2) - hematopoietic stem cell transplantation; graft vs host disease - antineoplastična sredstva - zalmoksis je indiciran kao dodatna terapija u haploidentical hematopoetskih matičnih stanica (hsct) odraslih bolesnika s visokog rizika hematoloških malignih bolesti.

Visudyne यूरोपीय संघ - क्रोएशियाई - EMA (European Medicines Agency)

visudyne

cheplapharm arzneimittel gmbh - verteporfin - myopia, degenerative; macular degeneration - ophthalmologicals - Визудин indiciran za liječenje:odrasli s экссудативной (vlažna) senilne makularne degeneracije (amd) s pretežno klasične subfoveal хориоидальной неоваскуляризации (ХНВ); ili odrasli s subfoveal хориоидальной неоваскуляризации sekundarne patološkog kratkovidnosti.

Septolete mentol 1 mg pastile क्रोएशिया - क्रोएशियाई - HALMED (Agencija za lijekove i medicinske proizvode)

septolete mentol 1 mg pastile

krka - farma d.o.o., radnička cesta 48, zagreb - benzalkonii klorida - pastila - 1 mg - urbroj: svaka pastila sadrži 1,0 mg benzalkonijevog klorida

Daunoblastina 2 mg/ml prašak i otapalo za otopinu za injekciju क्रोएशिया - क्रोएशियाई - HALMED (Agencija za lijekove i medicinske proizvode)

daunoblastina 2 mg/ml prašak i otapalo za otopinu za injekciju

pfizer croatia d.o.o., slavonska avenija 6, zagreb, hrvatska - daunorubicinklorid - prašak i otapalo za otopinu za injekciju - 2 mg/ml - urbroj: jedna bočica sadrži 20 mg daunorubicinklorida nakon rekonstitucije s 10 ml otapala jedna bočica sadrži 2 mg/ml daunorubicinklorida

Farmorubicin PFS 2 mg/ml otopina za injekciju/infuziju क्रोएशिया - क्रोएशियाई - HALMED (Agencija za lijekove i medicinske proizvode)

farmorubicin pfs 2 mg/ml otopina za injekciju/infuziju

pfizer croatia d.o.o., slavonska avenija 6, zagreb, hrvatska - epirubicinklorid - otopina za injekciju/infuziju - 2 mg/ml - urbroj: jedna bočica od 5 ml sadrži 10 mg epirubicinklorida; jedna bočica od 25 ml sadrži 50 mg epirubicinklorida