Euroopa Liit - portugali - EMA (European Medicines Agency)

ratiopharm gmbh - sildenafil - disfunção erétil - urologia - tratamento de homens com disfunção erétil, que é a incapacidade de alcançar ou manter uma ereção peniana suficiente para um desempenho sexual satisfatório. para que o sildenafil seja efetivo, é necessária uma estimulação sexual.

Euroopa Liit - portugali - EMA (European Medicines Agency)

teva gmbh - fumarato de dimetilo - multiple sclerosis, relapsing-remitting; multiple sclerosis - imunossupressores - dimethyl fumarate teva is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).

Euroopa Liit - portugali - EMA (European Medicines Agency)

boehringer ingelheim international gmbh - linagliptin, metformina - diabetes mellitus, tipo 2 - drogas usadas em diabetes - o tratamento de pacientes adultos com diabetes mellitus do tipo 2:jentadueto é indicado como adjuvante à dieta e ao exercício para melhorar o controlo glicémico em doentes adultos, inadequadamente controlados em sua máxima tolerada, a dose de metformina isoladamente, ou aqueles que já tenham sido tratados com a combinação de linagliptin e metformin. jentadueto é indicado em combinação com um sulphonylurea (eu. triplo terapia de combinação), como adjuvante da dieta e exercício em pacientes adultos inadequadamente controlados em sua máxima tolerada, a dose de metformina e uma sulphonylurea.

Euroopa Liit - portugali - EMA (European Medicines Agency)

biontech manufacturing gmbh - single-stranded, 5’-capped messenger rna produced using a cell-free in vitro transcription from the corresponding dna templates, encoding the viral spike (s) protein of sars-cov-2 - covid-19 virus infection - vacinas - comirnaty 30 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty original/omicron ba. 1 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older who have previously received at least a primary vaccination course against covid-19. comirnaty original/omicron ba. 4-5 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty original/omicron ba. 4-5 (1. 5/1. 5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty omicron xbb. 5 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty omicron xbb. 5 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 10 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years. o uso desta vacina deve ser de acordo com as recomendações oficiais.

Euroopa Liit - portugali - EMA (European Medicines Agency)

daiichi sankyo europe gmbh - trastuzumab deruxtecan - neoplasias do peito - agentes antineoplásicos - breast cancerher2-positive breast cancerenhertu as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic her2-positive breast cancer who have received one or more prior anti-her2-based regimens. her2-low breast cancerenhertu as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic her2-low breast cancer who have received prior chemotherapy in the metastatic setting or developed disease recurrence during or within 6 months of completing adjuvant chemotherapy (see section 4. non-small cell lung cancer (nsclc)enhertu as monotherapy is indicated for the treatment of adult patients with advanced nsclc whose tumours have an activating her2 (erbb2) mutation and who require systemic therapy following platinum-based chemotherapy with or without immunotherapy. gastric cancerenhertu as monotherapy is indicated for the treatment of adult patients with advanced her2-positive gastric or gastroesophageal junction (gej) adenocarcinoma who have received a prior trastuzumab-based regimen.

Euroopa Liit - portugali - EMA (European Medicines Agency)

biofrontera bioscience gmbh - cloridrato de ácido 5-aminolevulínico - keratosis, actinic; carcinoma, basal cell - agentes antineoplásicos - tratamento de queratose actínica de leve a moderada gravidade no rosto e couro cabeludo (olsen grau 1 para 2; ver secção 5. 1) e de campo cancerization em adultos. tratamento superficial e/ou nodular carcinoma basocelular inadequado para o tratamento cirúrgico devido a possíveis relacionadas com o tratamento, morbidade e/ou pobres resultado estético em adultos.

Euroopa Liit - portugali - EMA (European Medicines Agency)

merz pharmaceuticals gmbh - cloridrato de memantina - doença de alzheimer - outros medicamentos anti-demência - tratamento de pacientes com doença de alzheimer moderada a grave.

Euroopa Liit - portugali - EMA (European Medicines Agency)

otsuka novel products gmbh - delamanid - tuberculose, resistente a mutações múltiplas - antimicrobacterianos - deltyba is indicated for use as part of an appropriate combination regimen for pulmonary multi-drug resistant tuberculosis (mdr-tb) in adults, adolescents, children and infants with a body weight of at least 10 kg when an effective treatment regimen cannot otherwise be composed for reasons of resistance or tolerability (see sections 4. 2, 4. 4 e 5. deve ser tido em consideração a orientação oficial sobre o uso apropriado de agentes antibacterianos..

Euroopa Liit - portugali - EMA (European Medicines Agency)

eisai gmbh - eribulin - breast neoplasms; liposarcoma - agentes antineoplásicos - a monoterapia com halaven é indicada para o tratamento de pacientes com câncer de mama localmente avançado ou metastático que progrediu após pelo menos um regime quimioterapêutico para doença avançada (ver seção 5. terapia prévia deveria ter incluído uma antraciclina e um taxano a menos que os pacientes não fossem adequados para esses tratamentos. halaven é indicado para o tratamento de pacientes adultos com metastáticos lipossarcoma que recebeu antes de antraciclina contendo a terapia (a menos inadequado) para a avançada ou doença metastática (consulte a secção 5.

Euroopa Liit - portugali - EMA (European Medicines Agency)

boehringer ingelheim international gmbh - empagliflozin - diabetes mellitus, type 2; heart failure; renal insufficiency, chronic - drogas usadas em diabetes - type 2 diabetes mellitusjardiance is indicated for the treatment of adults with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exerciseas monotherapy when metformin is considered in addition to other medicinal products for the treatment of diabetesfor study results with respect to combinations of therapies, effects on glycaemic control, and cardiovascular and renal events, and the populations studied, see sections 4. 4, 4. 5 e 5. of the annex. heart failurejardiance is indicated in adults for the treatment of symptomatic chronic heart failure.  chronic kidney diseasejardiance is indicated in adults for the treatment of chronic kidney disease.