Kymriah Europos Sąjunga - ispanų - EMA (European Medicines Agency)

kymriah

novartis europharm limited - tisagenlecleucel - precursor b-cell lymphoblastic leukemia-lymphoma; lymphoma, large b-cell, diffuse - otros agentes antineoplásicos - 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.

Libtayo Europos Sąjunga - ispanų - EMA (European Medicines Agency)

libtayo

regeneron ireland designated activity company (dac) - cemiplimab - carcinoma, célula escamosa - agentes antineoplásicos - cutaneous squamous cell carcinomalibtayo as monotherapy is indicated for the treatment of adult patients with metastatic or locally advanced cutaneous squamous cell carcinoma (mcscc or lacscc) who are not candidates for curative surgery or curative radiation. basal cell carcinomalibtayo as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic basal cell carcinoma (labcc or mbcc) who have progressed on or are intolerant to a hedgehog pathway inhibitor (hhi). non-small cell lung cancerlibtayo as monotherapy is indicated for the first-line treatment of adult patients with non-small cell lung cancer (nsclc) expressing pd-l1 (in ≥ 50% tumour cells), with no egfr, alk or ros1 aberrations, who have:locally advanced nsclc who are not candidates for definitive chemoradiation, ormetastatic nsclc. libtayo in combination with platinum‐based chemotherapy is indicated for the first‐line treatment of adult patients with nsclc expressing pd-l1 (in ≥ 1% of tumour cells), with no egfr, alk or ros1 aberrations, who have:locally advanced nsclc who are not candidates for definitive chemoradiation, ormetastatic nsclc. cervical cancerlibtayo as monotherapy is indicated for the treatment of adult patients with recurrent or metastatic cervical cancer and disease progression on or after platinum-based chemotherapy.

Jemperli Europos Sąjunga - ispanų - EMA (European Medicines Agency)

jemperli

glaxosmithkline (ireland) limited - dostarlimab - endometrial neoplasms - antineoplastic agents and antibody drug conjugates - jemparli is indicated as monotherapy for the treatment of adult patients with mismatch repair deficient (dmmr)/microsatellite instability-high (msi h) recurrent or advanced endometrial cancer (ec) that has progressed on or following prior treatment with a platinum-containing regimen.

XEMBIFY 200 MG/ML SOLUCION INYECTABLE SUBCUTANEA Ispanija - ispanų - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

xembify 200 mg/ml solucion inyectable subcutanea

instituto grifols s.a. - inmunoglobulina humana normal - soluciÓn inyectable - 200 mg/ml inyectable 50 ml - inmunoglobulina humana normal 200 mg - inmunoglobulinas humanas normales para adm. extravascular

HEMAX 4000 UI Argentina - ispanų - ANMAT (Administración Nacional de Medicamentos, Alimentos y Tecnología Médica)

hemax 4000 ui

bio sidus s.a. - eritropoyetina - solucion inyectable - eritropoyetina 4000 ui / 2 ml

HEMAX 2000 UI Argentina - ispanų - ANMAT (Administración Nacional de Medicamentos, Alimentos y Tecnología Médica)

hemax 2000 ui

bio sidus s.a. - eritropoyetina - solucion inyectable - eritropoyetina humana 2000 ui / 1 ml

HYPERCRIT Argentina - ispanų - ANMAT (Administración Nacional de Medicamentos, Alimentos y Tecnología Médica)

hypercrit

bio sidus s.a. - eritropoyetina - pol liof - eritropoyetina humana recombinante 2000 ui