Chile - español - ISPC (Instituto de Salud Pública de Chile)

takeda chile s.p.a. - brentuximab vedotina - brentuximab vedotina (1) 50,0 mg - 1.- linfoma de hodgkin clásico (chl) en estadio iv no tratado previamente, en combinación con quimioterapia: adcetris está indicado para el tratamiento de pacientes adultos con chl en estadio iv no tratado previamente, en combinación con doxorrubicina, vinblastina y dacarbazina. 2.- consolidación del linfoma de hodgkin clásico (chl): adcetris está indicado para el tratamiento de pacientes adultos con chl con alto riesgo de recaída o progresión como consolidación después del trasplante autólogo de células madre hematopoyéticas (auto-hsct). 3.- linfoma de hodgkin clásico (chl) recidivante: adcetris está indicado para el tratamiento de pacientes adultos con chl después del fracaso del auto-hsct o después del fracaso de por lo menos dos regímenes previos de quimioterapia con múltiples agentes en pacientes que no son candidatos para el auto-hsct. 4.- linfoma anaplásico de células grandes sistémico (salcl) u otros linfomas periféricos de células t (ptcl) que expresan cd30, en combinación con quimioterapia no tratados previamente: adcetris está indicado para el tratamiento de pacientes adultos con salcl no tratado previamente u otro ptcl que expresa cd30, incluido el linfoma angioinmunoblástico de células t y el ptcl no especificado de otro modo, en combinación con ciclofosfamida, doxorrubicina y prednisona. 5.- linfoma anaplásico sistémico de células grandes recidivante (salcl): adcetris está indicado para el tratamiento de pacientes adultos con salcl después del fracaso de por lo menos un régimen de quimioterapia previa con múltiples agentes. 6.- linfoma anaplásico de células grandes cutáneo primario recidivante (pcalcl) o micosis fungoides (mf) que expresan cd30: adcetris está indicado para el tratamiento de pacientes adultos con pcalcl o mf que expresan cd30 que han recibido terapia sistémica previa.

Unión Europea - español - EMA (European Medicines Agency)

takeda pharma a/s - brentuximab vedotin - lymphoma, non-hodgkin; hodgkin disease - agentes antineoplásicos - hodgkin lymphomaadcetris is indicated for adult patients with previously untreated cd30+ stage iv hodgkin lymphoma (hl) in combination with doxorubicin, vinblastine and dacarbazine (avd). adcetris is indicated for the treatment of adult patients with cd30+ hl at increased risk of relapse or progression following autologous stem cell transplant (asct). adcetris is indicated for the treatment of adult patients with relapsed or refractory cd30+ hodgkin lymphoma (hl):following asct, orfollowing at least two prior therapies when asct or multi-agent chemotherapy is not a treatment option. systemic anaplastic large cell lymphomaadcetris in combination with cyclophosphamide, doxorubicin and prednisone (chp) is indicated for adult patients with previously untreated systemic anaplastic large cell lymphoma (salcl). adcetris is indicated for the treatment of adult patients with relapsed or refractory salcl. cutaneous t cell lymphomaadcetris is indicated for the treatment of adult patients with cd30+ cutaneous t cell lymphoma (ctcl) after at least 1 prior systemic therapy.

Venezuela - español - Instituto Nacional de Higiene

takeda s.r.l. - brentuximab vedotina - polvo liofilizado para concentrado para solucion para perfusion - 50 mg

Perú - español - DIGEMID (Dirección General de Medicamentos, Insumos y Drogas)

takeda s.r.l. - droguerÍa - brentuximab vedotina - concentrado para solucion para perfusion - 50mg - por vial - - brentuximab vedotina

Ecuador - español - Agencia Nacional de Regulación, Control y Vigilancia Sanitaria

takeda ecuador cia. ltda. ecuador - brentuximab vedotin 50 mg - polvo para concentrado para soluciÓn para perfusiÓn - cada vial contiene: brentuximab vedotin 50 mg

Unión Europea - español - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - nivolumab - melanoma; hodgkin disease; carcinoma, renal cell; carcinoma, non-small-cell lung; carcinoma, transitional cell; squamous cell carcinoma of head and neck; urologic neoplasms; mesothelioma; colorectal neoplasms - agentes antineoplásicos - melanomaopdivo as monotherapy or in combination with ipilimumab is indicated for the treatment of advanced (unresectable or metastatic) melanoma in adults and adolescents 12 years of age and older. relative to nivolumab monotherapy, an increase in progression free survival (pfs) and overall survival (os) for the combination of nivolumab with ipilimumab is established only in patients with low tumour pd-l1 expression. adjuvant treatment of melanomaopdivo as monotherapy is indicated for the adjuvant treatment of adults and adolescents 12 years of age and older with melanoma with involvement of lymph nodes or metastatic disease who have undergone complete resection. non-small cell lung cancer (nsclc)opdivo in combination with ipilimumab and 2 cycles of platinum-based chemotherapy is indicated for the first-line treatment of metastatic non-small cell lung cancer in adults whose tumours have no sensitising egfr mutation or alk translocation. opdivo as monotherapy is indicated for the treatment of locally advanced or metastatic non-small cell lung cancer after prior chemotherapy in adults. neoadjuvant treatment of nsclcopdivo in combination with platinum-based chemotherapy is indicated for the neoadjuvant treatment of resectable non-small cell lung cancer at high risk of recurrence in adult patients whose tumours have pd-l1 expression ≥ 1%. malignant pleural mesothelioma (mpm)opdivo in combination with ipilimumab is indicated for the first-line treatment of adult patients with unresectable malignant pleural mesothelioma. neoadjuvant treatment of nsclcopdivo in combination with platinum-based chemotherapy is indicated for the neoadjuvant treatment of resectable non-small cell lung cancer at high risk of recurrence in adult patients whose tumours have pd-l1 expression ≥ 1%. renal cell carcinoma (rcc)opdivo as monotherapy is indicated for the treatment of advanced renal cell carcinoma after prior therapy in adults. opdivo in combination with ipilimumab is indicated for the first-line treatment of adult patients with intermediate/poor risk advanced renal cell carcinoma. opdivo in combination with cabozantinib is indicated for the first-line treatment of adult patients with advanced renal cell carcinoma. classical hodgkin lymphoma (chl)opdivo as monotherapy is indicated for the treatment of adult patients with relapsed or refractory classical hodgkin lymphoma after autologous stem cell transplant (asct) and treatment with brentuximab vedotin. squamous cell cancer of the head and neck (scchn)opdivo as monotherapy is indicated for the treatment of recurrent or metastatic squamous cell cancer of the head and neck in adults progressing on or after platinum based therapy. urothelial carcinomaopdivo as monotherapy is indicated for the treatment of locally advanced unresectable or metastatic urothelial carcinoma in adults after failure of prior platinum containing therapy. adjuvant treatment of urothelial carcinomaopdivo as monotherapy is indicated for the adjuvant treatment of adults with muscle invasive urothelial carcinoma (miuc) with tumour cell pd-l1 expression ≥ 1%, who are at high risk of recurrence after undergoing radical resection of miuc. mismatch repair deficient (dmmr) or microsatellite instability-high (msi-h) colorectal cancer (crc)opdivo in combination with ipilimumab is indicated for the treatment of adult patients with mismatch repair deficient or microsatellite instability-high metastatic colorectal cancer after prior fluoropyrimidine based combination chemotherapy. oesophageal squamous cell carcinoma (oscc)opdivo in combination with ipilimumab is indicated for the first-line treatment of adult patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma with tumour cell pd-l1 expression ≥ 1%. opdivo in combination with fluoropyrimidine- and platinum-based combination chemotherapy is indicated for the first-line treatment of adult patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma with tumour cell pd-l1 expression ≥ 1%. opdivo as monotherapy is indicated for the treatment of adult patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma after prior fluoropyrimidine- and platinum-based combination chemotherapy. adjuvant treatment of oesophageal or gastro-oesophageal junction cancer (oc or gejc)opdivo as monotherapy is indicated for the adjuvant treatment of adult patients with oesophageal or gastro-oesophageal junction cancer who have residual pathologic disease following prior neoadjuvant chemoradiotherapy. gastric, gastro‑oesophageal junction (gej) or oesophageal adenocarcinomaopdivo in combination with fluoropyrimidine- and platinum-based combination chemotherapy is indicated for the first‑line treatment of adult patients with her2‑negative advanced or metastatic gastric, gastro‑oesophageal junction or oesophageal adenocarcinoma whose tumours express pd-l1 with a combined positive score (cps) ≥ 5.

Perú - español - DIGEMID (Dirección General de Medicamentos, Insumos y Drogas)

r.h. medica s.a. - solucion para inyeccion - por vial ; albumina humana 20.000000 g; - brentuximab vedotina

Perú - español - DIGEMID (Dirección General de Medicamentos, Insumos y Drogas)

bristol-myers squibb peru s.a. - droguerÍa -   nivolumab - solucion inyectable - 10 mg/ml - por vial ml - - nivolumab