União Europeia - português - EMA (European Medicines Agency)

sanofi winthrop industrie - dupilumab - dermatitis, atopic; prurigo; esophageal diseases; asthma; sinusitis - agentes para dermatite, excluindo corticosteróides - atopic dermatitisadults and adolescentsdupixent is indicated for the treatment of moderate-to-severe atopic dermatitis in adults and adolescents 12 years and older who are candidates for systemic therapy. children 6 months to 11 years of agedupixent is indicated for the treatment of severe atopic dermatitis in children 6 months to 11 years old who are candidates for systemic therapy. asthmaadults and adolescentsdupixent is indicated in adults and adolescents 12 years and older as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils and/or raised fraction of exhaled nitric oxide (feno), see section 5. 1, who are inadequately controlled with high dose inhaled corticosteroids (ics) plus another medicinal product for maintenance treatment. children 6 to 11 years of agedupixent is indicated in children 6 to 11 years old as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils and/or raised fraction of exhaled nitric oxide (feno), who are inadequately controlled with medium to high dose inhaled corticosteroids (ics) plus another medicinal product for maintenance treatment. chronic rhinosinusitis with nasal polyposis (crswnp)dupixent is indicated as an add-on therapy with intranasal corticosteroids for the treatment of adults with severe crswnp for whom therapy with systemic corticosteroids and/or surgery do not provide adequate disease control. prurigo nodularis (pn)dupixent is indicated for the treatment of adults with moderate-to-severe prurigo nodularis (pn) who are candidates for systemic therapy. eosinophilic esophagitis (eoe)dupixent is indicated for the treatment of eosinophilic esophagitis in adults and adolescents 12 years and older, weighing at least 40 kg, who are inadequately controlled by, are intolerant to, or who are not candidates for conventional medicinal therapy.

União Europeia - português - EMA (European Medicines Agency)

roche registration gmbh - metoxi polietileno glicol-epoetina beta - anemia; kidney failure, chronic - preparações antianêmicas - treatment of symptomatic anaemia associated with chronic kidney disease (ckd) in adult patients (see section 5. treatment of symptomatic anaemia associated with chronic kidney disease (ckd) in paediatric patients from 3 months to less than 18 years of age who are converting from another erythropoiesis stimulating agent (esa) after their haemoglobin level was stabilised with the previous esa (see section 5.

União Europeia - português - EMA (European Medicines Agency)

takeda pharma a/s - o citrato de fentanil - pain; cancer - analgésicos - instanyl é indicado para o gerenciamento da dor inovadora em adultos que já recebem manutenção de terapia com opióides para dor de câncer crônica. a dor inovadora é uma exacerbação transitória da dor que ocorre em um fundo de dor persistente, de outra forma controlada.  patients receiving maintenance opioid therapy are those who are taking at least 60 mg of oral morphine daily, at least 25 micrograms of transdermal fentanyl per hour, at least 30 mg oxycodone daily, at least 8 mg of oral hydromorphone daily or an equianalgesic dose of another opioid for a week or longer.

União Europeia - português - EMA (European Medicines Agency)

ecuphar nv - enflicoxib - produtos antiinflamatórios e anti-reumáticos - cães - for the treatment of pain and inflammation associated with osteoarthritis (or degenerative joint disease) in dogs.

União Europeia - português - EMA (European Medicines Agency)

astrazeneca ab - tezepelumab - asma - medicamentos para obstrutiva, doenças das vias respiratórias, - tezspire is indicated as an add-on maintenance treatment in adults and adolescents 12 years and older with severe asthma who are inadequately controlled despite high dose inhaled corticosteroids plus another medicinal product for maintenance treatment.

União Europeia - português - EMA (European Medicines Agency)

nordic group b.v. - tegafur, gimeracil, oteracil - neoplasias de estômago - agentes antineoplásicos - teysuno is indicated in adults:- for the treatment of advanced gastric cancer when given in combination with cisplatin (see section 5. - as monotherapy or in combination with oxaliplatin or irinotecan, with or without bevacizumab, for the treatment of patients with metastatic colorectal cancer for whom it is not possible to continue treatment with another fluoropyrimidine due to hand-foot syndrome or cardiovascular toxicity that developed in the adjuvant or metastatic setting.

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

abdi farma gmbh - ticagrelor - comprimido revestido por película - 90 mg - ticagrelor 90 mg - ticagrelor - genérico - duração do tratamento: longa duração

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

abdi farma gmbh - ticagrelor - comprimido revestido por película - 60 mg - ticagrelor 60 mg - ticagrelor - genérico - duração do tratamento: longa duração

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

abdi farma gmbh - ticagrelor - comprimido revestido por película - 90 mg - ticagrelor 90 mg - ticagrelor - genérico - duração do tratamento: longa duração

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

abdi farma gmbh - ticagrelor - comprimido revestido por película - 60 mg - ticagrelor 60 mg - ticagrelor - genérico - duração do tratamento: longa duração