União Europeia - português - EMA (European Medicines Agency)

mylan ireland limited - lenalidomida - mieloma múltiplo - imunossupressores - multiple myelomalenalidomide mylan as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation. lenalidomide mylan as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone is indicated for the treatment of adult patients with previously untreated multiple myeloma who are not eligible for transplant. lenalidomide mylan in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy. follicular lymphomalenalidomide mylan in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1-3a).

União Europeia - português - EMA (European Medicines Agency)

krka, d.d., novo mesto  - lenalidomide hydrochloride hydrate - multiple myeloma; lymphoma, follicular; myelodysplastic syndromes - imunossupressores - multiple myelomalenalidomide krka d. as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation. lenalidomide krka d. as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone (see section 4. 2) é indicado para o tratamento de pacientes adultos não tratados previamente com mieloma múltiplo que não são elegíveis para transplante. lenalidomide krka d. in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy. myelodysplastic syndromeslenalidomide krka d. as monotherapy is indicated for the treatment of adult patients with transfusion-dependent anemia due to low- or intermediate-1-risk myelodysplastic syndromes associated with an isolated deletion 5q cytogenetic abnormality when other therapeutic options are insufficient or inadequate. follicular lymphomalenalidomide krka d. in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a).

Brasil - português - ANVISA (Agência Nacional de Vigilância Sanitária)

glaxosmithkline brasil ltda - antineoplasicos citotoxicos

Brasil - português - ANVISA (Agência Nacional de Vigilância Sanitária)

camber farmaceutica ltda - bortezomibe - antineoplasicos citotoxicos

Brasil - português - ANVISA (Agência Nacional de Vigilância Sanitária)

eurofarma laboratÓrios s.a. - bortezomibe - agentes antineoplÁsicos e imunomoduladores

Brasil - português - ANVISA (Agência Nacional de Vigilância Sanitária)

janssen-cilag farmacÊutica ltda - daratumumabe - anticorpos monoclonais

União Europeia - português - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - pomalidomide - mieloma múltiplo - imunossupressores - imnovid em combinação com o bortezomib e a dexametasona é indicado no tratamento de doentes adultos com mieloma múltiplo que tenham recebido pelo menos um tratamento anterior regime, incluindo a lenalidomida. imnovid em associação com dexametasona é indicado no tratamento de pacientes adultos com mieloma múltiplo recidivante e refratário que receberam pelo menos dois regimes de tratamento prévios, incluindo lenalidomida e bortezomib, e demonstraram progressão da doença na última terapia.

União Europeia - português - EMA (European Medicines Agency)

stemline therapeutics b.v. - selinexor - mieloma múltiplo - agentes antineoplásicos - nexpovio is indicatedin combination with bortezomib and dexamethasone for the treatment of adult patients with multiple myeloma who have received at least one prior therapy. in combination with dexamethasone for the treatment of multiple myeloma in adult patients who have received at least four prior therapies and whose disease is refractory to at least two proteasome inhibitors, two immunomodulatory agents and an anti-cd38 monoclonal antibody, and who have demonstrated disease progression on the last therapy.

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

farmoz - sociedade técnico medicinal, s.a. - lenalidomida - cápsula - 10 mg - lenalidomida 10 mg - lenalidomide - genérico - duração do tratamento: longa duração

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

farmoz - sociedade técnico medicinal, s.a. - lenalidomida - cápsula - 15 mg - lenalidomida 15 mg - lenalidomide - genérico - duração do tratamento: longa duração