União Europeia - português - EMA (European Medicines Agency)

biogen netherlands b.v. - diroximel fumarate (biib098) - esclerose múltipla remitente-recorrente envio - imunossupressores - vumerity is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis (see section 5. 1 for important information on the populations for which efficacy has been established).

União Europeia - português - EMA (European Medicines Agency)

deciphera pharmaceuticals (netherlands) b.v. - ripretinib - tumores do estromal gastrointestinal - agentes antineoplásicos - qinlock is indicated for the treatment of adult patients with advanced gastrointestinal stromal tumour (gist) who have received prior treatment with three or more kinase inhibitors, including imatinib.

União Europeia - português - EMA (European Medicines Agency)

siga technologies netherlands b.v. - tecovirimat - poxviridae infections; cowpox; monkeypox; vaccinia; smallpox - antivirais para uso sistêmico - tecovirimat siga is indicated for the treatment of the following viral infections in adults and children with body weight at least 13 kg:- smallpox- monkeypox- cowpoxtecovirimat siga is also indicated to treat complications due to replication of vaccinia virus following vaccination against smallpox in adults and children with body weight at least 13 kg (see sections 4. 4 e 5. tecovirimat siga should be used in accordance with official recommendations.

União Europeia - português - EMA (European Medicines Agency)

otsuka pharmaceutical netherlands b.v. - voclosporin - lupus nephritis - imunossupressores - lupkynis is indicated in combination with mycophenolate mofetil for the treatment of adult patients with active class iii, iv or v (including mixed class iii/v and iv/v) lupus nephritis (ln).

União Europeia - português - EMA (European Medicines Agency)

taiho pharma netherlands b.v. - futibatinib - cholangiocarcinoma - agentes antineoplásicos - lytgobi monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic cholangiocarcinoma with a fibroblast growth factor receptor 2 (fgfr2) fusion or rearrangement that have progressed after at least one prior line of systemic therapy.

União Europeia - português - EMA (European Medicines Agency)

glaxosmithkline biologicals s.a.  - respiratory syncytial virus recombinant glycoprotein f stabilised in the pre-fusion conformation (rsvpref3) produced in chinese hamster ovary (cho) cells by recombinant dna technology - infecções respiratórias do vírus sincitial - vacinas - arexvy is indicated for active immunisation for the prevention of lower respiratory tract disease (lrtd) caused by respiratory syncytial virus in adults 60 years of age and older. o uso desta vacina deve ser de acordo com as recomendações oficiais.

União Europeia - português - EMA (European Medicines Agency)

otsuka pharmaceutical netherlands b.v. - cedazuridine, decitabine - leucemia, mieloide - agentes antineoplásicos - inaqovi is indicated as monotherapy for the treatment of adult patients with newly diagnosed acute myeloid leukaemia (aml) who are ineligible for standard induction chemotherapy.

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

curium netherlands b.v. - cloreto taloso (201tl) - solução injetável - 37 mbq/ml - cloreto taloso (201tl) 37 mbq/ml - thallium (201tl) chloride - radiofármaco - duração do tratamento: curta ou média duração

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

curium netherlands b.v. - cloreto taloso (201tl) - solução injetável - 37 mbq/ml - cloreto taloso (201tl) 37 mbq/ml - thallium (201tl) chloride - radiofármaco - duração do tratamento: curta ou média duração

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

curium netherlands b.v. - cloreto taloso (201tl) - solução injetável - 37 mbq/ml - cloreto taloso (201tl) 37 mbq/ml - thallium (201tl) chloride - radiofármaco - duração do tratamento: curta ou média duração