Enjaymo Unión Europea - portugués - EMA (European Medicines Agency)

enjaymo

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).

Tecvayli Unión Europea - portugués - EMA (European Medicines Agency)

tecvayli

janssen-cilag international n.v. - teclistamab - mieloma múltiplo - agentes antineoplásicos - tecvayli is indicated as monotherapy 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.

Amvuttra Unión Europea - portugués - EMA (European Medicines Agency)

amvuttra

alnylam netherlands b.v. - vutrisiran sodium - amyloid neuropathies, familial - outros medicamentos do sistema nervoso - treatment of hereditary transthyretin-mediated amyloidosis (hattr amyloidosis) in adult patients with stage 1 or stage 2 polyneuropathy.

Amoxicilina + Ácido Clavulânico Centrient 875 mg + 125 mg Comprimido revestido por película Portugal - portugués - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

amoxicilina + ácido clavulânico centrient 875 mg + 125 mg comprimido revestido por película

centrient pharmaceuticals netherlands b.v. - amoxicilina + Ácido clavulânico - comprimido revestido por película - 875 mg + 125 mg - amoxicilina tri-hidratada 1004.4 mg ; clavulanato de potássio, diluído com celulose microcristalina (1:1) 297.81 mg - amoxicillin and beta-lactamase inhibitor - genérico - duração do tratamento: curta ou média duração

Amoxicilina + Ácido Clavulânico Centrient 875 mg + 125 mg Comprimido revestido por película Portugal - portugués - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

amoxicilina + ácido clavulânico centrient 875 mg + 125 mg comprimido revestido por película

centrient pharmaceuticals netherlands b.v. - amoxicilina + Ácido clavulânico - comprimido revestido por película - 875 mg + 125 mg - amoxicilina tri-hidratada 1004.4 mg ; clavulanato de potássio, diluído com celulose microcristalina (1:1) 297.81 mg - amoxicillin and beta-lactamase inhibitor - genérico - duração do tratamento: curta ou média duração

Columvi Unión Europea - portugués - EMA (European Medicines Agency)

columvi

roche registration gmbh  - glofitamab - lymphoma, large b-cell, diffuse - agentes antineoplásicos - columvi as monotherapy is indicated for the treatment of adult patients with relapsed or refractory diffuse large b cell lymphoma (dlbcl), after two or more lines of systemic therapy.

Degarelix Accord Unión Europea - portugués - EMA (European Medicines Agency)

degarelix accord

accord healthcare s.l.u. - degarelix acetate - neoplasias prostáticas - other hormone antagonists and related agents - degarelix accord is a gonadotrophin releasing hormone (gnrh) antagonist indicated:for treatment of adult male patients with advanced hormone-dependent prostate cancer. for treatment of high-risk localised and locally advanced hormone dependent prostate cancer in combination with radiotherapy. as neo-adjuvant treatment prior to radiotherapy in patients with high-risk localised or locally advanced hormone dependent prostate cancer.

Memantine Mylan Unión Europea - portugués - EMA (European Medicines Agency)

memantine mylan

mylan pharmaceuticals limited - cloridrato de memantina - doença de alzheimer - other anti-dementia drugs, psychoanaleptics, - tratamento de pacientes com doença de alzheimer moderada a grave.

Revolade Unión Europea - portugués - EMA (European Medicines Agency)

revolade

novartis europharm limited - eltrombopag - purpura, trombocitopénica, idiopática - other systemic hemostatics, antihemorrhagics - revolade is indicated for the treatment of adult patients with primary immune thrombocytopenia (itp) who are refractory to other treatments (e. corticosteroids, immunoglobulins) (see sections 4. 2 e 5. revolade is indicated for the treatment of paediatric patients aged 1 year and above with primary immune thrombocytopenia (itp) lasting 6 months or longer from diagnosis and who are refractory to other treatments (e. corticosteroids, immunoglobulins) (see sections 4. 2 e 5. revolade is indicated in adult patients with chronic hepatitis c virus (hcv) infection for the treatment of thrombocytopenia, where the degree of thrombocytopenia is the main factor preventing the initiation or limiting the ability to maintain optimal interferon-based therapy (see sections 4. 4 and 5. revolade is indicated in adult patients with acquired severe aplastic anaemia (saa) who were either refractory to prior immunosuppressive therapy or heavily pretreated and are unsuitable for haematopoietic stem cell transplantation (see section 5.

Takhzyro Unión Europea - portugués - EMA (European Medicines Agency)

takhzyro

takeda pharmaceuticals international ag ireland branch - lanadelumab - angioedemas, hereditário - other hematological agents - takhzyro is indicated for routine prevention of recurrent attacks of hereditary angioedema (hae) in patients aged 2 years and older.