Kymriah Európska únia - lotyština - EMA (European Medicines Agency)

kymriah

novartis europharm limited - tisagenlecleucel - precursor b-cell lymphoblastic leukemia-lymphoma; lymphoma, large b-cell, diffuse - other antineoplastic agents - 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 Európska únia - lotyština - EMA (European Medicines Agency)

yescarta

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

Zynteglo Európska únia - lotyština - EMA (European Medicines Agency)

zynteglo

bluebird bio (netherlands) b.v. - autologās cd34+ šūnu bagātināts iedzīvotāju, kas satur asinsrades cilmes šūnas, transduced ar lentiglobin bb305 lentiviral vektoru kodēšanas beta-a-t87q-globin gēnu - beta-talasēmija - other hematological agents - zynteglo ir indicēts, lai ārstētu pacientu, 12 gadi un vecāki ar asins pārliešanu atkarīgas no β thalassaemia (tdt), kas nav β0/β0 genotipa, kuriem hematopoētisko cilmes šūnu (vak) transplantācija ir lietderīgi, bet cilvēka leikocītu antigēnu (hla)-saskaņota saistīti hsc donoru nav pieejama.

Breyanzi Európska únia - lotyština - 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 - antineoplastiski līdzekļi - 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.

Carvykti Európska únia - lotyština - EMA (European Medicines Agency)

carvykti

janssen-cilag international nv - ciltacabtagene autoleucel - multiple mieloma - 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.

Boostrix Polio suspensija injekcijām Lotyšsko - lotyština - Zāļu valsts aģentūra

boostrix polio suspensija injekcijām

glaxosmithkline latvia, sia, latvija - difterijas, stingumkrampju, acelulāra garā klepus un poliomielīta (inaktivēta) vakcīna (adsorbēta) - suspensija injekcijām

Boostrix Polio suspensija injekcijām pilnšļircē Lotyšsko - lotyština - Zāļu valsts aģentūra

boostrix polio suspensija injekcijām pilnšļircē

glaxosmithkline biologicals s.a., belgium - difterijas, stingumkrampju, acelulāra garā klepus un poliomielīta (inaktivēta) vakcīna (adsorbēta) - suspensija injekcijām pilnšļircē

Pentaxim pulveris un suspensija injekciju suspensijas pagatavošanai pilnšļircē Lotyšsko - lotyština - Zāļu valsts aģentūra

pentaxim pulveris un suspensija injekciju suspensijas pagatavošanai pilnšļircē

sanofi pasteur, france - difterijas, stingumkrampju, garā klepus, poliomielīta (inaktivēta) un b tipa haemophilus influenzae konjugēta vakcīna (adsorbēta) - pulveris un suspensija injekciju suspensijas pagatavošanai pilnšļircē

Infanrix-IPV + Hib pulveris un suspensija injekciju suspensijas pagatavošanai Lotyšsko - lotyština - Zāļu valsts aģentūra

infanrix-ipv + hib pulveris un suspensija injekciju suspensijas pagatavošanai

glaxosmithkline biologicals s.a., belgium - difterijas, stingumkrampju, acelulāra garā klepus, poliomielīta (inaktivēta) un b tipa haemophilus influenzae konjugēta vakcīna (adsorbēta) - pulveris un suspensija injekciju suspensijas pagatavošanai

Infanrix polio suspensija injekcijām pilnšļircē Lotyšsko - lotyština - Zāļu valsts aģentūra

infanrix polio suspensija injekcijām pilnšļircē

glaxosmithkline biologicals s.a., belgium - difterijas, stingumkrampju, acelulāra garā klepus un poliomielīta (inaktivēta) vakcīna (adsorbēta) - suspensija injekcijām pilnšļircē