पुर्तगाल - पुर्तगाली - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

synthon, b.v. - tansulosina - comprimido de libertação prolongada - 0.4 mg - tansulosina, cloridrato 0.4 mg - tamsulosin - genérico - duração do tratamento: longa duração

पुर्तगाल - पुर्तगाली - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

synthon, b.v. - tansulosina - comprimido de libertação prolongada - 0.4 mg - tansulosina, cloridrato 0.4 mg - tamsulosin - genérico - duração do tratamento: longa duração

पुर्तगाल - पुर्तगाली - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

synthon, b.v. - tansulosina - comprimido de libertação prolongada - 0.4 mg - tansulosina, cloridrato 0.4 mg - tamsulosin - genérico - duração do tratamento: longa duração

पुर्तगाल - पुर्तगाली - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

synthon, b.v. - tansulosina - comprimido de libertação prolongada - 0.4 mg - tansulosina, cloridrato 0.4 mg - tamsulosin - genérico - duração do tratamento: longa duração

यूरोपीय संघ - पुर्तगाली - EMA (European Medicines Agency)

koanaa healthcare gmbh - o imatinib mesilate - leukemia, myelogenous, chronic, bcr-abl positive; precursor cell lymphoblastic leukemia-lymphoma; myelodysplastic-myeloproliferative diseases; hypereosinophilic syndrome; dermatofibrosarcoma; gastrointestinal stromal tumors - agentes antineoplásicos - imatinib koanaa is indicated for the treatment ofadult and paediatric patients with newly diagnosed philadelphia chromosome (bcr-abl) positive (ph+) chronic myeloid leukaemia (cml) for whom bone marrow transplantation is not considered as the first line of treatment. adult and paediatric patients with ph+ cml in chronic phase after failure of interferon-alpha therapy, or in accelerated phase or blast crisis. adult and paediatric patients with newly diagnosed philadelphia chromosome positive acute lymphoblastic leukaemia (ph+ all) integrated with chemotherapy. adult patients with relapsed or refractory ph+ all as monotherapy. adult patients with myelodysplastic/myeloproliferative diseases (mds/mpd) associated with platelet-derived growth factor receptor (pdgfr) gene re-arrangements. adult patients with advanced hypereosinophilic syndrome (hes) and/or chronic eosinophilic leukaemia (cel) with fip1l1-pdgfrα rearrangement. the effect of imatinib on the outcome of bone marrow transplantation has not been determined. imatinib koanaa is indicated forthe treatment of adult patients with kit (cd 117) positive unresectable and/or metastatic malignant gastrointestinal stromal tumours (gist). the adjuvant treatment of adult patients who are at significant risk of relapse following resection of kit (cd117)-positive gist. os pacientes que têm um baixo ou muito baixo risco de recorrência não deve receber tratamento adjuvante. the treatment of adult patients with unresectable dermatofibrosarcoma protuberans (dfsp) and adult patients with recurrent and/or metastatic dfsp who are not eligible for surgery. in adult and paediatric patients, the effectiveness of imatinib is based on overall haematological and cytogenetic response rates and progression-free survival in cml, on haematological and cytogenetic response rates in ph+ all, mds/mpd, on haematological response rates in hes/cel and on objective response rates in adult patients with unresectable and/or metastatic gist and dfsp and on recurrence-free survival in adjuvant gist. the experience with imatinib in patients with mds/mpd associated with pdgfr gene re-arrangements is very limited (see section 5. exceto em recém-diagnosticados lmc em fase crónica, não há ensaios clínicos controlados demonstrando um benefício clínico ou aumento da sobrevivência para essas doenças.

यूरोपीय संघ - पुर्तगाली - EMA (European Medicines Agency)

roche registration gmbh - atezolizumab - carcinoma, transitional cell; carcinoma, non-small-cell lung; urologic neoplasms; breast neoplasms; small cell lung carcinoma - agentes antineoplásicos - urothelial carcinomatecentriq as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic urothelial carcinoma (uc):- after prior platinum containing chemotherapy, or - who are considered cisplatin ineligible, and whose tumours have a pd-l1 expression ≥ 5% (see section 5. non-small cell lung cancer tecentriq, in combination with bevacizumab, paclitaxel and carboplatin, is indicated for the first-line treatment of adult patients with metastatic non-squamous non small cell lung cancer (nsclc). in patients with egfr mutant or alk-positive nsclc, tecentriq, in combination with bevacizumab, paclitaxel and carboplatin, is indicated only after failure of appropriate targeted therapies (see section 5. tecentriq, in combination with nab paclitaxel and carboplatin, is indicated for the first line treatment of adult patients with metastatic non-squamous nsclc who do not have egfr mutant or alk positive nsclc (see section 5. tecentriq as monotherapy is indicated for the first-line treatment of adult patients with metastatic non-small cell lung cancer (nsclc) whose tumours have a pd-l1 expression ≥ 50% tumour cells (tc) or ≥ 10% tumour-infiltrating immune cells (ic) and who do not have egfr mutant or alk-positive nsclc (see section 5. tecentriq como monoterapia é indicado para o tratamento de pacientes adultos com localmente avançado ou metastático, nsclc após quimioterapia prévia. patients with egfr mutant or alk positive nsclc should also have received targeted therapies before receiving tecentriq (see section 5. small cell lung cancertecentriq, in combination with carboplatin and etoposide, is indicated for the first-line treatment of adult patients with extensive-stage small cell lung cancer (es-sclc) (see section 5. hepatocellular carcinomatecentriq, in combination with bevacizumab, is indicated for the treatment of adult patients with advanced or unresectable hepatocellular carcinoma (hcc) who have not received prior systemic therapy (see section 5. urothelial carcinomatecentriq as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic urothelial carcinoma (uc):- after prior platinum containing chemotherapy, or- who are considered cisplatin ineligible, and whose tumours have a pd-l1 expression ≥ 5% (see section 5. non-small cell lung cancertecentriq as monotherapy is indicated for the first-line treatment of adult patients with metastatic non-small cell lung cancer (nsclc) whose tumours have a pd-l1 expression ≥ 50% tumour cells (tc) or ≥ 10% tumour-infiltrating immune cells (ic) and who do not have egfr mutant or alk-positive nsclc (see section 5. tecentriq como monoterapia é indicado para o tratamento de pacientes adultos com localmente avançado ou metastático, nsclc após quimioterapia prévia. patients with egfr mutant or alk positive nsclc should also have received targeted therapies before receiving tecentriq (see section 5. triple-negative breast cancertecentriq in combination with nab-paclitaxel is indicated for the treatment of adult patients with unresectable locally advanced or metastatic triple-negative breast cancer (tnbc) whose tumours have pd-l1 expression ≥ 1% and who have not received prior chemotherapy for metastatic disease.

पुर्तगाल - पुर्तगाली - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

venus pharma gmbh - cefuroxima - pó para solução injetável ou para perfusão - 750 mg - cefuroxima sódica 750 mg - cefuroxime - genérico - duração do tratamento: curta ou média duração

पुर्तगाल - पुर्तगाली - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

venus pharma gmbh - cefuroxima - pó para solução injetável ou para perfusão - 750 mg - cefuroxima sódica 750 mg - cefuroxime - genérico - duração do tratamento: curta ou média duração

पुर्तगाल - पुर्तगाली - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

venus pharma gmbh - cefuroxima - pó para solução injetável ou para perfusão - 750 mg - cefuroxima sódica 750 mg - cefuroxime - genérico - duração do tratamento: curta ou média duração

पुर्तगाल - पुर्तगाली - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

venus pharma gmbh - cefuroxima - pó para solução injetável ou para perfusão - 1500 mg - cefuroxima sódica 1500 mg - cefuroxime - genérico - duração do tratamento: curta ou média duração