União Europeia - português - EMA (European Medicines Agency)

stada arzneimittel ag - budesonide, micronised - glomerulonephritis, iga - antidiarreicos, intestinal antiinflamatórios / anti infeccioso agentes - kinpeygo is indicated for the treatment of primary immunoglobulin a (iga) nephropathy (igan) in adults at risk of rapid disease progression with a urine protein-to-creatinine ratio (upcr) ≥1. 5 g/gram.

União Europeia - português - EMA (European Medicines Agency)

roche registration gmbh - mosunetuzumab - linfoma, folicular - antineoplastic agents, monoclonal antibodies - lunsumio as monotherapy is indicated for the treatment of adult patients with relapsed or refractory follicular lymphoma (fl) who have received at least two prior systemic therapies.

União Europeia - português - EMA (European Medicines Agency)

janssen-cilag international nv - ciltacabtagene autoleucel - mieloma múltiplo - carvykti is indicated for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least three prior therapies, including an immunomodulatory agent, a proteasome inhibitor and an anti-cd38 antibody and have demonstrated disease progression on the last therapy.

União Europeia - português - EMA (European Medicines Agency)

ptc therapeutics international limited - eladocagene exuparvovec - metabolismo de aminoácidos, erros nascidos - enzymes, other alimentary tract and metabolism products - upstaza is indicated for the treatment of patients aged 18 months and older with a clinical, molecular, and genetically confirmed diagnosis of aromatic l amino acid decarboxylase (aadc) deficiency with a severe phenotype (see section 5.

União Europeia - português - EMA (European Medicines Agency)

sanofi b.v. - sutimlimab - hemolysis; anemia, hemolytic, autoimmune - imunossupressores - enjaymo is indicated for the treatment of haemolytic anaemia in adult patients with cold agglutinin disease (cad).

União Europeia - português - EMA (European Medicines Agency)

pierre fabre medicament - tabelecleucel - lymphoproliferative disorders - ebvallo is indicated as monotherapy for treatment of adult and paediatric patients 2 years of age and older with relapsed or refractory epstein-barr virus positive post-transplant lymphoproliferative disease (ebv+ ptld) who have received at least one prior therapy. for solid organ transplant patients, prior therapy includes chemotherapy unless chemotherapy is inappropriate.

União Europeia - português - EMA (European Medicines Agency)

amryt pharmaceuticals dac - octreotide acetate - acromegalia - hormonas e análises pituitárias e hipotalâmicas - mycapssa is indicated for maintenance treatment in adult patients with acromegaly who have responded to and tolerated treatment with somatostatin analogues.

União Europeia - português - EMA (European Medicines Agency)

y-mabs therapeutics a/s - iodine (131i) omburtamab - neuroblastoma - rádiofarmacêutica terapêutica - treatment of neuroblastoma.

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

recordati rare diseases - hemina - concentrado para solução para perfusão - 250 mg/10 ml - hemina 25 mg/ml - heme products - derivado do sangue e plasma humano - duração do tratamento: curta ou média duração

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

sigillata ltd. - oxicodona - comprimido de libertação prolongada - 5 mg - oxicodona, cloridrato 5 mg - oxycodone - genérico - duração do tratamento: longa duração