欧盟 - 葡萄牙文 - EMA (European Medicines Agency)

idorsia pharmaceuticals deutschland gmbh - daridorexant hydrochloride - transtornos de iniciação e manutenção do sono - psicolepticos - quviviq is indicated for the treatment of adult patients with insomnia characterised by symptoms present for at least 3 months and considerable impact on daytime functioning.

欧盟 - 葡萄牙文 - EMA (European Medicines Agency)

merck europe b.v. - tepotinib hydrochloride monohydrate - carcinoma, pulmão de células não pequenas - agentes antineoplásicos - tepmetko as monotherapy is indicated for the treatment of adult patients with advanced non-small cell lung cancer (nsclc) harbouring alterations leading to mesenchymal-epithelial transition factor gene exon 14 (metex14) skipping, who require systemic therapy following prior treatment with immunotherapy and/or platinum-based chemotherapy.

欧盟 - 葡萄牙文 - EMA (European Medicines Agency)

gilead sciences international ltd  - emtricitabine, rilpivirine hydrochloride, tenofovir disoproxil fumarate - infecções por hiv - antivirais para uso sistêmico - a eviplera está indicada para o tratamento de adultos infectados com o vírus da imunodeficiência humana tipo 1 (hiv-1) sem mutações conhecidas associadas à resistência à classe de inibidores de transcriptase reversa não nucleósidos (nnrti), tenofovir ou emtricitabina e com carga viral ≤ 100,000 cópias de arn do hiv-1 / ml. tal como acontece com outros medicamentos anti-retrovirais, testes de resistência genotípica e / ou dados históricos de resistência devem orientar o uso de eviplera.

欧盟 - 葡萄牙文 - EMA (European Medicines Agency)

lupin europe gmbh - mexiletine hydrochloride - miotônica transtornos - terapia cardíaca - namuscla é indicado para o tratamento sintomático da miotonia em pacientes adultos com não-distrófico miotônica transtornos.

欧盟 - 葡萄牙文 - EMA (European Medicines Agency)

krka, d.d., novo mesto  - lenalidomide hydrochloride monohydrate - multiple myeloma; lymphoma, follicular - imunossupressores - multiple myelomalenalidomide krka d. novo mesto as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation. lenalidomide krka d. novo mesto as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone (see section 4. 2) é indicado para o tratamento de pacientes adultos não tratados previamente com mieloma múltiplo que não são elegíveis para transplante. lenalidomide krka d. novo mesto in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy. follicular lymphomalenalidomide krka d. novo mesto in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a). multiple myelomalenalidomide krka d. novo mesto as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation. lenalidomide krka d. novo mesto as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone (see section 4. 2) é indicado para o tratamento de pacientes adultos não tratados previamente com mieloma múltiplo que não são elegíveis para transplante. lenalidomide krka d. novo mesto in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy. follicular lymphomalenalidomide krka d. novo mesto in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a).

欧盟 - 葡萄牙文 - EMA (European Medicines Agency)

dipharma arzneimittel gmbh - sapropterin dihydrochloride - fenilcetonurias - outro aparelho digestivo e metabolismo produtos, - sapropterin dipharma is indicated for the treatment of hyperphenylalaninaemia (hpa) in adults and paediatric patients of all ages with phenylketonuria (pku) who have been shown to be responsive to such treatment. sapropterin dipharma is also indicated for the treatment of hyperphenylalaninaemia (hpa) in adults and paediatric patients of all ages with tetrahydrobiopterin (bh4) deficiency who have been shown to be responsive to such treatment.

欧盟 - 葡萄牙文 - EMA (European Medicines Agency)

accord healthcare s.l.u. - sitagliptin hydrochloride - diabetes mellitus, tipo 2 - drogas usadas em diabetes - for adult patients with type 2 diabetes mellitus, sitagliptin accord is indicated to improve glycaemic control:as monotherapy:- in patients inadequately controlled by diet and exercise alone and for whom metformin is inappropriate due to contraindications or intolerance. as dual oral therapy in combination with:- metformin when diet and exercise plus metformin alone do not provide adequate glycaemic control. - a sulphonylurea when diet and exercise plus maximal tolerated dose of a sulphonylurea alone do not provide adequate glycaemic control and when metformin is inappropriate due to contraindications or intolerance. - a peroxisome proliferator-activated receptor gamma (ppary) agonist (i. a thiazolidinedione) when use of a ppary agonist is appropriate and when diet and exercise plus the ppary agonist alone do not provide adequate glycaemic control. as triple oral therapy in combination with:- a sulphonylurea and metformin when diet and exercise plus dual therapy with these medicinal products do not provide adequate glycaemic control. - a ppary agonist and metformin when use of a ppary agonist is appropriate and when diet and exercise plus dual therapy with these medicinal products do not provide adequate glycaemic control. sitagliptin accord is also indicated as add-on to insulin (with or without metformin) when diet and exercise plus stable dose of insulin do not provide adequate glycaemic control.

欧盟 - 葡萄牙文 - EMA (European Medicines Agency)

janssen-cilag international nv - canagliflozin, metformin hydrochloride - diabetes mellitus, tipo 2 - drogas usadas em diabetes - vokanamet é indicado em adultos com idade entre 18 e mais anos, com diabetes mellitus tipo 2, como adjuvante à dieta e ao exercício para melhorar o controlo glicémico:em pacientes não controlados adequadamente, em seus máximo tolerado em doses de metformina alonein pacientes em seu máximo tolerado em doses de metformina, juntamente com outros glicose reduzindo medicamentos, incluindo insulina, quando estes não fornecem adequado controlo glicémico. em doentes já a serem tratados com a combinação de canagliflozin e a metformina como separar tabletsfor resultados do estudo com relação a combinação de terapias, efeitos no controlo glicémico e eventos cardiovasculares, e as populações estudadas, consulte as secções 4. 4, 4. 5 e 5.

欧盟 - 葡萄牙文 - EMA (European Medicines Agency)

abbvie deutschland gmbh & co. kg - dalbavancin hydrochloride - soft tissue infections; skin diseases, bacterial - antibacterianos para uso sistémico, - tratamento de infecções bacterianas agudas da pele e da pele (absssi) em adultos.

欧盟 - 葡萄牙文 - EMA (European Medicines Agency)

orion corporation - ropinirole hydrochloride - agentes dopaminérgicos, agonistas da dopamina - cães - a indução de vômitos em cães.