البرازيل - البرتغالية - ANVISA (Agência Nacional de Vigilância Sanitária)

sanofi medley farmacÊutica ltda. - outros medicamentos de acao no aparelho cardiovascular

البرازيل - البرتغالية - ANVISA (Agência Nacional de Vigilância Sanitária)

ranbaxy farmacÊutica ltda - outros medicamentos de acao no aparelho cardiovascular

الاتحاد الأوروبي - البرتغالية - EMA (European Medicines Agency)

the medicines company uk ltd - bivalirudin - síndrome coronariana aguda - agentes antitrombóticos - angiox é indicado como um anticoagulante em pacientes adultos submetidos à intervenção coronária percutânea (pci), incluindo pacientes com infarto do miocárdio de elevação do segmento st (stemi) submetidos à icp primária. angiox é também indicado para o tratamento de pacientes adultos com angina instável / não-st-segmento de elevação de infarto do miocárdio (ua / nstemi) prevista para urgência ou de intervenção precoce. angiox deve ser administrado com aspirina e clopidogrel.

الاتحاد الأوروبي - البرتغالية - 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.

الاتحاد الأوروبي - البرتغالية - 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.

البرتغال - البرتغالية - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

covex, s.a. - vinpocetina - comprimido - 10 mg - vinpocetina 10 mg - vinpocetine - n/a - duração do tratamento: longa duração

البرتغال - البرتغالية - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

covex, s.a. - vinpocetina - comprimido - 5 mg - vinpocetina 5 mg - vinpocetine - n/a - duração do tratamento: longa duração

البرتغال - البرتغالية - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

covex, s.a. - vinpocetina - comprimido - 5 mg - vinpocetina 5 mg - vinpocetine - n/a - duração do tratamento: longa duração

البرتغال - البرتغالية - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

covex, s.a. - vinpocetina - comprimido - 10 mg - vinpocetina 10 mg - vinpocetine - n/a - duração do tratamento: longa duração

البرازيل - البرتغالية - ANVISA (Agência Nacional de Vigilância Sanitária)

bristol-myers squibb farmacÊutica ltda - anticoagulantes