PSILO-BALSAM 10MG/G Gel チェコ共和国 - チェコ語 - SUKL (Státní ústav pro kontrolu léčiv)

psilo-balsam 10mg/g gel

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

MEDOVERT 20MG/40MG Tableta チェコ共和国 - チェコ語 - SUKL (Státní ústav pro kontrolu léčiv)

medovert 20mg/40mg tableta

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

Stelfonta 欧州連合 - チェコ語 - EMA (European Medicines Agency)

stelfonta

qbiotics netherlands b.v. - tigilanol tiglate - tigilanol tiglate - psi - pro léčbu non-resekabilním, non-metastatický (kdo staging) podkožní mastocytů se nachází na nebo distální k lokti, nebo hleznu, a non-resekabilním, non metastazující kožní žírných buněk nádory u psů.

Kymriah 欧州連合 - チェコ語 - EMA (European Medicines Agency)

kymriah

novartis europharm limited - tisagenlecleucel - precursor b-cell lymphoblastic leukemia-lymphoma; lymphoma, large b-cell, diffuse - další antineoplastické látky - kymriah is indicated for the treatment of:• paediatric and young adult patients up to and including 25 years of age with b cell acute lymphoblastic leukaemia (all) that is refractory, in relapse post transplant or in second or later relapse. • adult patients with relapsed or refractory diffuse large b cell lymphoma (dlbcl) after two or more lines of systemic therapy. • adult patients with relapsed or refractory follicular lymphoma (fl) after two or more lines of systemic therapy.

Yescarta 欧州連合 - チェコ語 - 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 欧州連合 - チェコ語 - 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 欧州連合 - チェコ語 - 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 欧州連合 - チェコ語 - 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.

MOTILIUM 10MG Potahovaná tableta チェコ共和国 - チェコ語 - SUKL (Státní ústav pro kontrolu léčiv)

motilium 10mg potahovaná tableta

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

Columvi 欧州連合 - チェコ語 - EMA (European Medicines Agency)

columvi

roche registration gmbh  - glofitamab - lymphoma, large b-cell, diffuse - antineoplastická činidla - columvi 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.