PSILO-BALSAM 10MG/G Gel Jamhuri ya Cheki - Kicheki - SUKL (Státní ústav pro kontrolu léčiv)

psilo-balsam 10mg/g gel

stada arzneimittel ag, bad vilbel array - 510 difenhydramin-hydrochlorid - gel - 10mg/g - difenhydramin

Rimadyl 50.0 mg/ml Injekční roztok Jamhuri ya Cheki - Kicheki - USKVBL (Ústav Pro Státní Kontrolu Veterinárních Biopreparátů A Léčiv)

rimadyl 50.0 mg/ml injekční roztok

zoetis Česká republika s.r.o. (2) - karprofen - injekční roztok - deriváty kyseliny propionové - kočky, psi

MOTILIUM 10MG Potahovaná tableta Jamhuri ya Cheki - Kicheki - SUKL (Státní ústav pro kontrolu léčiv)

motilium 10mg potahovaná tableta

janssen-cilag s.r.o., praha array - 4991 domperidon - potahovaná tableta - 10mg - domperidon

Vyxeos liposomal (previously known as Vyxeos) Umoja wa Ulaya - Kicheki - EMA (European Medicines Agency)

vyxeos liposomal (previously known as vyxeos)

jazz pharmaceuticals ireland limited - daunorubicin hydrochloride, cytarabine - leukemie, myeloidní, akutní - antineoplastická činidla - vyxeos lipozomální je indikován k léčbě dospělých pacientů s nově diagnostikovaným, terapie související s akutní myeloidní leukémií (t-aml), nebo aml s myelodysplasie-související změny (aml-mrc).

Oncaspar Umoja wa Ulaya - Kicheki - EMA (European Medicines Agency)

oncaspar

les laboratoires servier - pegaspargase - prekurzorová buněčná lymfoblastická leukémie-lymfom - antineoplastická činidla - přípravek oncaspar je indikován jako součást antineoplastické kombinované léčby u akutní lymfoblastické leukémie (all) u pediatrických pacientů od narození do 18 let a dospělých pacientů.

MEDOVERT 20MG/40MG Tableta Jamhuri ya Cheki - Kicheki - SUKL (Státní ústav pro kontrolu léčiv)

medovert 20mg/40mg tableta

medochemie ltd., limassol array - 363 cinarizin; 498 dimenhydrinÁt - tableta - 20mg/40mg - cinarizin, kombinace

Yescarta Umoja wa Ulaya - Kicheki - 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.

Tecartus Umoja wa Ulaya - Kicheki - 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).

Lunsumio Umoja wa Ulaya - Kicheki - EMA (European Medicines Agency)

lunsumio

roche registration gmbh - mosunetuzumab - lymfom, folikulární - 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.

Carvykti Umoja wa Ulaya - Kicheki - EMA (European Medicines Agency)

carvykti

janssen-cilag international nv - ciltacabtagene autoleucel - mnohočetný myelom - 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.