Liên Minh Châu Âu - Tiếng Bồ Đào Nha - EMA (European Medicines Agency)

sfl pharmaceuticals deutschland gmbh - nyxthracis - anthrax - imune soros e imunoglobulinas, - obiltoxaximab sfl is indicated in combination with appropriate antibacterial drugs in all age groups for treatment of inhalational anthrax due to bacillus anthracis (see section 5. obiltoxaximab sfl is indicated in all age groups for post-exposure prophylaxis of inhalational anthrax when alternative therapies are not appropriate or are not available (see section 5.

Liên Minh Châu Âu - Tiếng Bồ Đào Nha - 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.

Liên Minh Châu Âu - Tiếng Bồ Đào Nha - EMA (European Medicines Agency)

accord healthcare s.l.u. - dasatinib - precursor cell lymphoblastic leukemia-lymphoma; leukemia, myelogenous, chronic, bcr-abl positive - agentes antineoplásicos - dasatinib accord is indicated for the treatment of adult patients with:• ph+ acute lymphoblastic leukaemia (all) with resistance or intolerance to prior therapy. dasatinib accord is indicated for the treatment of paediatric patients with:• newly diagnosed ph+ all in combination with chemotherapy.

Liên Minh Châu Âu - Tiếng Bồ Đào Nha - EMA (European Medicines Agency)

accord healthcare s.l.u. - dasatinib - precursor cell lymphoblastic leukemia-lymphoma; leukemia, myelogenous, chronic, bcr-abl positive - agentes antineoplásicos - dasatinib accordpharma is indicated for the treatment of adult patients with: newly diagnosed philadelphia chromosome positive (ph+) chronic myelogenous leukaemia (cml) in the chronic phase.  chronic, accelerated or blast phase cml with resistance or intolerance to prior therapy including imatinib.  ph+ acute lymphoblastic leukaemia (all) and lymphoid blast cml with resistance or intolerance to prior therapy. dasatinib accordpharma is indicated for the treatment of paediatric patients with: newly diagnosed ph+ cml in chronic phase (ph+ cml-cp) or ph+ cml-cp resistant or intolerant to prior therapy including imatinib.  newly diagnosed ph+ all in combination with chemotherapy.

Liên Minh Châu Âu - Tiếng Bồ Đào Nha - EMA (European Medicines Agency)

mylan pharmaceuticals limited - teriflunomide - esclerose múltipla remitente-recorrente envio - imunossupressores - teriflunomide mylan is indicated for the treatment of adult patients and paediatric patients aged 10 years and older (body weight > 40 kg) with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 of the smpc for important information on the population for which efficacy has been established).

Liên Minh Châu Âu - Tiếng Bồ Đào Nha - EMA (European Medicines Agency)

accord healthcare s.l.u. - teriflunomide - esclerose múltipla remitente-recorrente envio - imunosupressão, seletiva imunosupressão - teriflunomide accord is indicated for the treatment of adult patients and paediatric patients aged 10 years and older with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 for important information on the population for which efficacy has been established).

Bồ Đào Nha - Tiếng Bồ Đào Nha - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

bluefish pharmaceuticals ab - bisoprolol - comprimido - 5 mg - bisoprolol, fumarato 5 mg - bisoprolol - genérico - duração do tratamento: longa duração

Bồ Đào Nha - Tiếng Bồ Đào Nha - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

bluefish pharmaceuticals ab - bisoprolol - comprimido - 5 mg - bisoprolol, fumarato 5 mg - bisoprolol - genérico - duração do tratamento: longa duração

Bồ Đào Nha - Tiếng Bồ Đào Nha - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

towa pharmaceutical, s.a. - etoricoxib - comprimido revestido por película - 30 mg - etoricoxib 30 mg - etoricoxib - genérico - duração do tratamento: curta ou média duração

Bồ Đào Nha - Tiếng Bồ Đào Nha - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

towa pharmaceutical, s.a. - etoricoxib - comprimido revestido por película - 30 mg - etoricoxib 30 mg - etoricoxib - genérico - duração do tratamento: curta ou média duração