Zydelig União Europeia - português - EMA (European Medicines Agency)

zydelig

gilead sciences ireland uc - idelalisib - lymphoma, non-hodgkin; leukemia, lymphocytic, chronic, b-cell - antineoplastic agents, other antineoplastic agents - zydelig is indicated in combination with an anti‑cd20 monoclonal antibody (rituximab or ofatumumab) for the treatment of adult patients with chronic lymphocytic leukaemia (cll):who have received at least one prior therapy, oras first line treatment in the presence of 17p deletion or tp53 mutation in patients who are not eligible for any other therapies. zydelig is indicated as monotherapy for the treatment of adult patients with follicular lymphoma (fl) that is refractory to two prior lines of treatment.

Celvapan União Europeia - português - EMA (European Medicines Agency)

celvapan

nanotherapeutics bohumil, s.r.o. - whole virion influenza vaccine, inactivated containing antigen of strain a/california/07/2009 (h1n1)v - disease outbreaks; influenza, human; immunization - vacinas - profilaxia da gripe causada pelo vírus a (h1n1) v 2009. celvapan deve ser usado de acordo com orientação oficial.

OENOTHERA BIENNIS Brasil - português - ANVISA (Agência Nacional de Vigilância Sanitária)

oenothera biennis

zenimport comercio importacao e exportacao ltda - fitoterapico simples

Lorviqua União Europeia - português - EMA (European Medicines Agency)

lorviqua

pfizer europe ma eeig - lorlatinib - carcinoma, pulmão de células não pequenas - antineoplastic agents, protein kinase inhibitors - lorviqua as monotherapy is indicated for the treatment of adult patients with anaplastic lymphoma kinase (alk)‑positive advanced non‑small cell lung cancer (nsclc) previously not treated with an alk inhibitor. lorviqua as monotherapy is indicated for the treatment of adult patients with alk‑positive advanced nsclc whose disease has progressed after:alectinib or ceritinib as the first alk tyrosine kinase inhibitor (tki) therapy; orcrizotinib and at least one other alk tki.

Calquence União Europeia - português - EMA (European Medicines Agency)

calquence

astrazeneca ab - acalabrutinib - leucemia, linfocítica, crônica, células b - antineoplastic agents, protein kinase inhibitors, - calquence as monotherapy or in combination with obinutuzumab is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (cll). calquence as monotherapy is indicated for the treatment of adult patients with chronic lymphocytic leukaemia (cll) who have received at least one prior therapy.

Jemperli União Europeia - português - 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.

Lunsumio União Europeia - português - EMA (European Medicines Agency)

lunsumio

roche registration gmbh - mosunetuzumab - linfoma, folicular - 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.

Vanflyta União Europeia - português - EMA (European Medicines Agency)

vanflyta

daiichi sankyo europe gmbh - quizartinib dihydrochloride - leucemia, mieloide - antineoplastic agents, protein kinase inhibitors - vanflyta is indicated in combination with standard cytarabine and anthracycline induction and standard cytarabine consolidation chemotherapy, followed by vanflyta single-agent maintenance therapy for adult patients with newly diagnosed acute myeloid leukaemia (aml) that is flt3-itd positive.

Cisplatina Hikma 0.5 mg/ml Concentrado para solução para perfusão Portugal - português - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

cisplatina hikma 0.5 mg/ml concentrado para solução para perfusão

hikma farmacêutica (portugal), s.a. - cisplatina - concentrado para solução para perfusão - 0.5 mg/ml - cisplatina 0.5 mg/ml - cisplatin - genérico - duração do tratamento: longa duração

Cisplatina Hikma 0.5 mg/ml Concentrado para solução para perfusão Portugal - português - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

cisplatina hikma 0.5 mg/ml concentrado para solução para perfusão

hikma farmacêutica (portugal), s.a. - cisplatina - concentrado para solução para perfusão - 0.5 mg/ml - cisplatina 0.5 mg/ml - cisplatin - genérico - duração do tratamento: longa duração