Portugal - português - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

ferrer internacional s.a. - Ácido acetilsalicílico + atorvastatina + ramipril - cápsula - 100 mg + 40 mg + 5 mg - ramipril 5 mg ; Ácido acetilsalicílico 100 mg ; atorvastatina cálcica tri-hidratada 43.38 mg - atorvastatin, acetylsalicylic acid and ramipril - n/a - duração do tratamento: longa duração

Portugal - português - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

teva b.v. - rosuvastatina + Ácido acetilsalicílico - cápsula - 20 mg + 100 mg - rosuvastatina cálcica 20.8 mg ; Ácido acetilsalicílico 100 mg - rosuvastatin and acetylsalicylic acid - n/a - duração do tratamento: longa duração

Portugal - português - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

teva b.v. - rosuvastatina + Ácido acetilsalicílico - cápsula - 20 mg + 100 mg - rosuvastatina cálcica 20.8 mg ; Ácido acetilsalicílico 100 mg - rosuvastatin and acetylsalicylic acid - n/a - duração do tratamento: longa duração

Portugal - português - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

ferrer internacional s.a. - Ácido acetilsalicílico + atorvastatina + ramipril - cápsula - 100 mg + 20 mg + 2.5 mg - atorvastatina cálcica tri-hidratada 21.69 mg ; ramipril 2.5 mg ; Ácido acetilsalicílico 100 mg - atorvastatin, acetylsalicylic acid and ramipril - n/a - duração do tratamento: longa duração

Portugal - português - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

ferrer internacional s.a. - Ácido acetilsalicílico + atorvastatina + ramipril - cápsula - 100 mg + 20 mg + 5 mg - ramipril 5 mg ; atorvastatina cálcica tri-hidratada 21.69 mg ; Ácido acetilsalicílico 100 mg - atorvastatin, acetylsalicylic acid and ramipril - n/a - duração do tratamento: longa duração

Portugal - português - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

laboratório medinfar - produtos farmacêuticos, s.a. - rosuvastatina + Ácido acetilsalicílico - cápsula - 10 mg + 100 mg - rosuvastatina cálcica 10.4 mg ; Ácido acetilsalicílico 100 mg - rosuvastatin and acetylsalicylic acid - n/a - duração do tratamento: longa duração

União Europeia - português - EMA (European Medicines Agency)

mylan ireland limited - rivaroxaban - venous thromboembolism; pulmonary embolism; acute coronary syndrome; stroke; coronary artery disease; peripheral arterial disease; atrial fibrillation - agentes antitrombóticos - rivaroxaban mylan co-administered with acetylsalicylic acid (asa) alone or with asa plus clopidogrel or ticlopidine, is indicated for the prevention of atherothrombotic events in adult patients after an acute coronary syndrome (acs) with elevated cardiac biomarkers.  rivaroxaban mylan co-administered with acetylsalicylic acid (asa), is indicated for the prevention of atherothrombotic events in adult patients with coronary artery disease (cad) or symptomatic peripheral artery disease (pad) at high risk of ischaemic events.  ------prevention of venous thromboembolism (vte) in adult patients undergoing elective hip or knee replacement surgery.  treatment of deep vein thrombosis (dvt) and pulmonary embolism (pe), and prevention of recurrent dvt and pe in adults. -------adults prevention of stroke and systemic embolism in adult   patients with non-valvular atrial fibrillation with one or more risk factors, such as congestive heart failure, hypertension, age ≥ 75 years, diabetes mellitus, prior stroke or transient ischaemic attack. paediatric population treatment of venous thromboembolism (vte) and prevention of vte recurrence in children and adolescents aged less than 18 years and weighing from 30 kg to 50 kg after at least 5 days of initial parenteral anticoagulation treatment. paediatric population treatment of venous thromboembolism (vte) and prevention of vte recurrence in children and adolescents aged less than 18 years and weighing more than 50 kg after at least 5 days of initial parenteral anticoagulation treatment.

União Europeia - português - EMA (European Medicines Agency)

bayer ag - rivaroxaban - arthroplasty, replacement; venous thromboembolism - agentes antitrombóticos - xarelto, co-administrada com ácido acetilsalicílico (asa) sozinho ou com asa mais clopidogrel ou ticlopidina, é indicada para a prevenção de eventos aterotrombóticos em pacientes adultos, após uma síndrome coronária aguda (sca), com elevação de biomarcadores cardíacos. xarelto, co-administered with acetylsalicylic acid (asa), is indicated for the prevention of atherothrombotic events in adult patients with coronary artery disease (cad) or symptomatic peripheral artery disease (pad) at high risk of ischaemic events. prevenção de tromboembolismo venoso (vte) em pacientes adultos submetidos à cirurgia eletiva de substituição de quadril ou joelho. tratamento da trombose venosa profunda (tvp) e embolia pulmonar (pe), e na prevenção da tvp recorrente e pe em adultos. adultsprevention of stroke and systemic embolism in adult patients with non-valvular atrial fibrillation with one or more risk factors, such as congestive heart failure, hypertension, age ≥ 75 years, diabetes mellitus, prior stroke or transient ischaemic attack. paediatric population treatment of venous thromboembolism (vte) and prevention of vte recurrence in children and adolescents aged less than 18 years and weighing from 30 kg to 50 kg after at least 5 days of initial parenteral anticoagulation treatment. paediatric population treatment of venous thromboembolism (vte) and prevention of vte recurrence in children and adolescents aged less than 18 years and weighing more than 50 kg after at least 5 days of initial parenteral anticoagulation treatment.

União Europeia - português - EMA (European Medicines Agency)

accord healthcare s.l.u. - rivaroxaban - acute coronary syndrome; coronary artery disease; peripheral arterial disease; venous thromboembolism; stroke; atrial fibrillation; pulmonary embolism - agentes antitrombóticos - prevenção de tromboembolismo venoso (vte) em pacientes adultos submetidos à cirurgia eletiva de substituição de quadril ou joelho. tratamento da trombose venosa profunda (tvp) e embolia pulmonar (pe), e na prevenção da tvp recorrente e pe em adultos. (see section 4. 4 for haemodynamically unstable pe patients. tratamento da trombose venosa profunda (tvp) e embolia pulmonar (pe), e na prevenção da tvp recorrente e pe em adultos. (see section 4. 4 para haemodynamically instável pe pacientes). adultsprevention of stroke and systemic embolism in adult patients with non valvular atrial fibrillation with one or more risk factors, such as congestive heart failure, hypertension, age ≥ 75 years, diabetes mellitus, prior stroke or transient ischaemic attack. tratamento da trombose venosa profunda (tvp) e embolia pulmonar (pe), e na prevenção da tvp recorrente e pe em adultos. (see section 4. 4 for haemodynamically unstable pe patients. )paediatric populationtreatment of venous thromboembolism (vte) and prevention of vte recurrence in children and adolescents aged less than 18 years and weighing from 30 kg to 50 kg after at least 5 days of initial parenteral anticoagulation treatment. rivaroxaban accord, co administered with acetylsalicylic acid (asa) alone or with asa plus ticlopidine, is indicated for the prevention of atherothrombotic events in adult patients after an acute coronary syndrome (acs) with elevated cardiac biomarkers (see sections 4. 3, 4. 4 e 5. rivaroxaban accord, co administered with acetylsalicylic acid (asa), is indicated for the prevention of atherothrombotic events in adult patients with coronary artery disease (cad) or symptomatic peripheral artery disease (pad) at high risk of ischaemic events. adultsprevention of stroke and systemic embolism in adult patients with non-valvular atrial fibrillation with one or more risk factors, such as congestive heart failure, hypertension, age ≥ 75 years, diabetes mellitus, prior stroke or transient ischaemic attack. tratamento da trombose venosa profunda (tvp) e embolia pulmonar (pe), e na prevenção da tvp recorrente e pe em adultos. (see section 4. 4 for haemodynamically unstable pe patients. )paediatric populationtreatment of venous thromboembolism (vte) and prevention of vte recurrence in children and adolescents aged less than 18 years and weighing more than 50 kg after at least 5 days of initial parenteral anticoagulation treatment.

Portugal - português - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

elpen pharmaceutical co. inc. - ticagrelor - comprimido revestido por película - 60 mg - ticagrelor 60 mg - ticagrelor - genérico - duração do tratamento: longa duração