Ευρωπαϊκή Ένωση - Ισπανικά - EMA (European Medicines Agency)

merck europe b.v. - avelumab - tumores neuroendocrinos - otros agentes antineoplásicos, anticuerpos monoclonales - bavencio está indicado como monoterapia para el tratamiento de pacientes adultos con cáncer metastásico carcinoma de células de merkel (mcc). bavencio en combinación con axitinib está indicado para el tratamiento de primera línea de pacientes adultos con carcinoma avanzado de células renales (rcc). bavencio is indicated as monotherapy for the first‑line maintenance treatment of adult patients with locally advanced or metastatic urothelial carcinoma (uc) who are progression-free following platinum‑based chemotherapy.

Ευρωπαϊκή Ένωση - Ισπανικά - EMA (European Medicines Agency)

bayer ag - sorafenib - carcinoma, hepatocellular; carcinoma, renal cell - agentes antineoplásicos - hepatocelular carcinomanexavar está indicado para el tratamiento del carcinoma hepatocelular. de células renales carcinomanexavar está indicado para el tratamiento de pacientes con carcinoma avanzado de células renales en los que han fracasado antes de interferón-alfa o interleucina-2 basado en la terapia o se consideran adecuados para la terapia. diferenciado de tiroides carcinomanexavar está indicado para el tratamiento de pacientes con progresiva, localmente avanzado o metastásico, diferenciado (papilar/folicular/células de hürthle) de carcinoma de tiroides, refractario al yodo radioactivo.

Ευρωπαϊκή Ένωση - Ισπανικά - EMA (European Medicines Agency)

recordati netherlands b.v. - tivozanib - carcinoma, células renales - agentes antineoplásicos - fotivda está indicado para el tratamiento de primera línea de pacientes adultos con carcinoma avanzado de células renales (rcc) y para pacientes adultos que vegfr y mtor vía inhibidor no siguen la progresión de la enfermedad después de un tratamiento previo con terapia del cytokine para rcc avanzado. tratamiento de carcinoma de células renales avanzado.

Ευρωπαϊκή Ένωση - Ισπανικά - EMA (European Medicines Agency)

pfizer europe ma eeig  - axitinib - carcinoma, células renales - inhibidores de la proteína quinasa - inlyta is indicated for the treatment of adult patients with advanced renal cell carcinoma (rcc) after failure of prior treatment with sunitinib or a cytokine.

Ευρωπαϊκή Ένωση - Ισπανικά - EMA (European Medicines Agency)

pfizer europe ma eeig - bevacizumab - colorectal neoplasms; breast neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell; uterine cervical neoplasms - agentes antineoplásicos - zirabev en combinación con fluoropirimidina basado en la quimioterapia está indicada para el tratamiento de pacientes adultos con carcinoma metastásico de colon o recto. zirabev en combinación con paclitaxel está indicado para el tratamiento de primera línea de pacientes adultos con cáncer de mama metastásico. para más información de como humanos, factor de crecimiento epidérmico 2 (her2) estado de. zirabev, además de la quimioterapia basada en platino, está indicado para el tratamiento de primera línea de pacientes adultos con irresecables avanzado, metastásico o recurrente no-pequeño cáncer de pulmón de células distinto predominantemente de células escamosas de la histología. zirabev en combinación con interferón alfa-2a está indicado para el tratamiento de primera línea de pacientes adultos con avanzado y/o metastásico, cáncer de células renales. zirabev, en combinación con paclitaxel y cisplatino o, alternativamente, paclitaxel y topotecan en pacientes que no pueden recibir de platino de la terapia, está indicado para el tratamiento de pacientes adultos con persistente, recurrente o metastásico, carcinoma del cuello uterino.

Ευρωπαϊκή Ένωση - Ισπανικά - EMA (European Medicines Agency)

astellas pharma europe b.v. - tacrolimus - rechazo del injerto - inmunosupresores - profilaxis del rechazo de trasplantes en receptores de aloinjerto de adultos y pediátricos, renales, hepáticos o cardíacos. tratamiento del rechazo de aloinjertos resistente a los tratamientos con otros medicamentos inmunosupresores en pacientes adultos y pediátricos.

Ευρωπαϊκή Ένωση - Ισπανικά - EMA (European Medicines Agency)

ceva santé animale - espironolactona - diuréticos - perros - para el uso en combinación con la terapia estándar (incluido el soporte diurético, cuando sea necesario) para el tratamiento de la insuficiencia cardíaca congestiva causada por la regurgitación valvular en perros.

Ευρωπαϊκή Ένωση - Ισπανικά - EMA (European Medicines Agency)

novartis europharm ltd. - amlodipino, valsartán, hidroclorotiazida - hipertensión - antagonistas de angiotensina ii, llano, antagonistas de angiotensina ii, combinaciones - tratamiento de la hipertensión esencial como terapia de sustitución en pacientes adultos cuya presión arterial se controla adecuadamente en la combinación de amlodipino, valsartán e hidroclorotiazida (hct), tomada como tres formulaciones del solo-componente o como una dos componentes y una formulación monocomponente.

Ευρωπαϊκή Ένωση - Ισπανικά - EMA (European Medicines Agency)

novartis europharm ltd - valsartan, amlodipine (as amlodipine besilate) - hipertensión - agentes que actúan sobre el sistema renina-angiotensina - el tratamiento de la hipertensión esencial. imprida está indicada en pacientes cuya presión arterial no está controlada adecuadamente con amlodipino o valsartán en monoterapia.

Ευρωπαϊκή Ένωση - Ισπανικά - 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.