Čilė - ispanų - ISPC (Instituto de Salud Pública de Chile)

pfizer chile s.a. - palbociclib - palbociclib 100,000 mg núcleo: - está indicado en combinación con la terapia endocrina para el tratamiento del cáncer de mama avanzado o metastásico con receptor de hormona (hr) positivo y receptor 2 del factor de crecimiento epidérmico humano (her2) negativo: - con un inhibidor de la aromatasa como terapia endocrina inicial en mujeres postmenopáusicas; o - con fulvestrant en mujeres que recibieron tratamiento anterior.

Čilė - ispanų - ISPC (Instituto de Salud Pública de Chile)

pfizer chile s.a. - palbociclib - palbociclib 125,000 mg núcleo - está indicado en combinación con la terapia endocrina para el tratamiento del cáncer de mama avanzado o metastásico con receptor de hormona (hr) positivo y receptor 2 del factor de crecimiento epidérmico humano (her2) negativo: - con un inhibidor de la aromatasa como terapia endocrina inicial en mujeres postmenopáusicas; o - con fulvestrant en mujeres que recibieron tratamiento anterior.

Čilė - ispanų - ISPC (Instituto de Salud Pública de Chile)

pfizer chile s.a. - palbociclib - palbociclib 75,000 mg núcleo - está indicado en combinación con la terapia endocrina para el tratamiento del cáncer de mama avanzado o metastásico con receptor de hormona (hr) positivo y receptor 2 del factor de crecimiento epidérmico humano (her2) negativo: -con un inhibidor de la aromatasa como terapia endocrina inicial en mujeres postmenopáusicas; o -con fulvestrant en mujeres que recibieron tratamiento anterior.

Čilė - ispanų - ISPC (Instituto de Salud Pública de Chile)

pentafarma s.a. - bicarbonato sodico; calcio cloruro; glucosa; magnesio cloruro; sodio cloruro - bicarbonato de sodio 0,29400 g; cloruro de calcio dihidrato 0,02573 g; cloruro de magnesio hexahidrato 0,01017 g; cloruro de sodio 0,57860 g - insuficiencia renal crónica (descompensada) en fase terminal de cualquier etiología, tratada con diálisis peritoneal.

Čilė - ispanų - ISPC (Instituto de Salud Pública de Chile)

pentafarma s.a. - bicarbonato sodico; calcio cloruro; glucosa; magnesio cloruro; sodio cloruro - bicarbonato de sodio 0,29400 g; cloruro de calcio dihidrato 0,02573 g; cloruro de magnesio hexahidrato 0,01017 g; cloruro de sodio 0,57860 g; glucosa monohidrato 2,50000 g - insuficiencia renal crónica (descompensada) en fase terminal de cualquier etiología, tratada con diálisis peritoneal.

Čilė - ispanų - ISPC (Instituto de Salud Pública de Chile)

pentafarma s.a. - bicarbonato sodico; calcio cloruro; glucosa; magnesio cloruro; sodio cloruro - bicarbonato de sodio 0,29400 g; cloruro de calcio dihidrato 0,02573 g; cloruro de magnesio hexahidrato 0,01017 g; cloruro de sodio 0,57860 g; glucosa monohidrato 4,67500 g - insuficiencia renal crónica (descompensada) en fase terminal de cualquier etiología, tratada con diálisis peritoneal.

Ispanija - ispanų - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

ratiopharm españa, s.a. - micofenolato de mofetilo - excipientes: croscarmelosa sodica,laurilsulfato de sodio,laurilsulfato de sodio,propilenglicol,potasio, hidroxido de - inmunosupresores - inmunosupresores selectivos - Ácido micofenólico

Ispanija - ispanų - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

ratiopharm españa, s.a. - micofenolato de mofetilo - excipientes: croscarmelosa sodica - inmunosupresores - inmunosupresores selectivos - Ácido micofenólico

Europos Sąjunga - ispanų - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - el ipilimumab - melanoma; carcinoma, renal cell; carcinoma, non-small-cell lung; mesothelioma, malignant; colorectal neoplasms - agentes antineoplásicos - melanomayervoy as monotherapy or combination with nivolumab is indicated for the treatment of advanced (unresectable or metastatic) melanoma in adults and adolescents 12 years of age and older (see section 4.  yervoy in combination with nivolumab is indicated for the treatment of advanced (unresectable or metastatic) melanoma in adults. 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 (see sections 4. 4 y 5. renal cell carcinoma (rcc)yervoy in combination with nivolumab is indicated for the first-line treatment of adult patients with intermediate/poor-risk advanced renal cell carcinoma (see section 5. non-small cell lung cancer (nsclc)yervoy in combination with nivolumab 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. malignant pleural mesothelioma (mpm)yervoy in combination with nivolumab is indicated for the first-line treatment of adult patients with unresectable malignant pleural mesothelioma. mismatch repair deficient (dmmr) or microsatellite instability-high (msi-h) colorectal cancer (crc)yervoy in combination with nivolumab 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 (see section 5. oesophageal squamous cell carcinoma (oscc)yervoy in combination with nivolumab 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%.

Europos Sąjunga - ispanų - 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.