Yescarta Europese Unie - Tsjechisch - EMA (European Medicines Agency)

yescarta

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

GHRYVELIN (previously Macimorelin Aeterna Zentaris) Europese Unie - Tsjechisch - EMA (European Medicines Agency)

ghryvelin (previously macimorelin aeterna zentaris)

atnahs pharma netherlands b.v. - macimorelin acetát - diagnostické techniky, endokrinní - macimorelin - tento léčivý přípravek je určen pouze pro diagnostické účely.  ghryvelin is indicated for the diagnosis of growth hormone deficiency (ghd) in adults.

Trepulmix Europese Unie - Tsjechisch - EMA (European Medicines Agency)

trepulmix

scipharm sàrl - treprostinil sodný - hypertenze, plicní - antitrombotické činidla - treatment of adult patients with who functional class (fc) iii or iv and:inoperable chronic thromboembolic pulmonary hypertension (cteph), orpersistent or recurrent cteph after surgical treatmentto improve exercise capacity.

Vaxchora Europese Unie - Tsjechisch - EMA (European Medicines Agency)

vaxchora

bavarian nordic a/s - vibrio cholerae, napětí cvd 103-hgr, žít - cholera - vakcíny - vaxchora is indicated for active immunisation against disease caused by vibrio cholerae serogroup o1 in adults and children aged 2 years and older. tato vakcína by měla být použita v souladu s oficiálními doporučeními.

Lyumjev (previously Liumjev) Europese Unie - Tsjechisch - EMA (European Medicines Agency)

lyumjev (previously liumjev)

eli lilly nederland b.v. - inzulín lispro - diabetes mellitus - léky užívané při diabetu - léčba diabetes mellitus u dospělých, dospívajících a dětí ve věku 1 roku a starší. léčba diabetes mellitus u dospělých.

Daurismo Europese Unie - Tsjechisch - EMA (European Medicines Agency)

daurismo

pfizer europe ma eeig - glasdegib maleate - leukemie, myeloidní, akutní - antineoplastická činidla - daurismo is indicated, in combination with low-dose cytarabine, for the treatment of newly diagnosed de novo or secondary acute myeloid leukaemia (aml) in adult patients who are not candidates for standard induction chemotherapy.

Insulin aspart Sanofi Europese Unie - Tsjechisch - EMA (European Medicines Agency)

insulin aspart sanofi

sanofi winthrop industrie - inzulin aspart - diabetes mellitus - léky užívané při diabetu - insulin aspart sanofi is indicated for the treatment of diabetes mellitus in adults, adolescents and children aged 1 year and above.

Tecartus Europese Unie - Tsjechisch - 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) - lymfom, mantle-cell - antineoplastická činidla - 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).

Kirsty (previously Kixelle) Europese Unie - Tsjechisch - EMA (European Medicines Agency)

kirsty (previously kixelle)

biosimilar collaborations ireland limited - inzulin aspart - diabetes mellitus - léky užívané při diabetu - kirsty is indicated for treatment of diabetes mellitus in adults, adolescents and children aged 1 year and above.

Gavreto Europese Unie - Tsjechisch - EMA (European Medicines Agency)

gavreto

roche registration gmbh  - pralsetinib - karcinom, plicní jiná než malobuněčná - antineoplastická činidla - gavreto is indicated as monotherapy for the treatment of adult patients with rearranged during transfection (ret) fusion-positive advanced non-small cell lung cancer (nsclc) not previously treated with a ret inhibitor.