Brasilien - portugisisk - ANVISA (Agência Nacional de Vigilância Sanitária)

janssen-cilag farmacÊutica ltda - bortezomibe - antineoplasicos citotoxicos

Den Europæiske Union - portugisisk - EMA (European Medicines Agency)

baxter holding b.v. - cloridrato de doxorrubicina - sarcoma, kaposi; multiple myeloma; ovarian neoplasms; breast neoplasms - agentes antineoplásicos - caelyx peguilado lipossomas é indicado:como monoterapia para pacientes com câncer de mama metastático, onde há um aumento do risco cardíaco;para o tratamento avançado de câncer de ovário em mulheres que não conseguiram uma primeira-linha platinum-base de quimioterapia regime;em combinação com o bortezomib para o tratamento de progressiva mieloma múltiplo em pacientes que receberam pelo menos uma terapêutica prévia e que já passou ou são inadequados para transplante de medula óssea;para tratamento da aids relacionados ao sarcoma de kaposi (sk) em pacientes com baixa contagem de células cd4 (.

Den Europæiske Union - portugisisk - EMA (European Medicines Agency)

accord healthcare s.l.u. - doxorubicin hydrochloride, liposomal - ovarian neoplasms; sarcoma, kaposi; multiple myeloma - doxorubicin - zolsketil pegylated liposomal is a medicine used to treat the following types of cancer in adults:• breast cancer that has spread to other parts of the body in patients at risk of heart problems. zolsketil pegylated liposomal is used on its own for this disease;• advanced ovarian cancer in women whose previous treatment including a platinum-based cancer medicine has stopped working;• multiple myeloma (a cancer of the white blood cells in the bone marrow), in patients with progressive disease who have received at least one other treatment in the past and have already had, or are unsuitable for, a bone marrow transplantation. zolsketil pegylated liposomal is used in combination with bortezomib (another cancer medicine);• kaposi’s sarcoma in patients with aids who have a very damaged immune system. kaposi’s sarcoma is a cancer that causes abnormal tissue to grow under the skin, on moist body surfaces or on internal organs. zolsketil pegylated liposomal contains the active substance doxorubicin and is a ‘hybrid medicine’. this means that it is similar to a ‘reference medicine’ containing the same active substance called adriamycin. however, in zolsketil pegylated liposomal the active substance is enclosed in tiny fatty spheres called liposomes, whereas this is not the case for adriamycin.

Den Europæiske Union - portugisisk - EMA (European Medicines Agency)

yes pharmaceutical development services gmbh - cloridrato de doxorrubicina - breast neoplasms; ovarian neoplasms; multiple myeloma; sarcoma, kaposi - agentes antineoplásicos - celdoxome pegylated liposomal is indicated in adults:as monotherapy for patients with metastatic breast cancer, where there is an increased cardiac risk. or treatment of advanced ovarian cancer in women who have failed a first-line platinum-based chemotherapy regimen. in combination with bortezomib for the treatment of progressive multiple myeloma in patients who have received at least one prior therapy and who have already undergone or are unsuitable for bone marrow transplant. for treatment of aids-related kaposi’s sarcoma (ks) in patients with low cd4 counts (< 200 cd4 lymphocytes/mm3) and extensive mucocutaneous or visceral disease. celdoxome pegylated liposomal may be used as first-line systemic chemotherapy, or as second line chemotherapy in aids-ks patients with disease that has progressed with, or in patients intolerant to, prior combination systemic chemotherapy comprising at least two of the following agents: a vinca alkaloid, bleomycin and standard doxorubicin (or other anthracycline).

Brasilien - portugisisk - ANVISA (Agência Nacional de Vigilância Sanitária)

cipla brasil importadora e distribuidora de medicamentos ltda - bortezomibe - antineoplasico

Den Europæiske Union - portugisisk - EMA (European Medicines Agency)

pharmaand gmbh - panacetato lactato anidro - mieloma múltiplo - agentes antineoplásicos - farydak, em combinação com bortezomib e dexametasona, é indicado para o tratamento de pacientes adultos com mieloma múltiplo recidivante e / ou refratário que receberam pelo menos dois regimes anteriores, incluindo bortezomib e um agente imunomodulador. farydak, em combinação com bortezomib e dexametasona, é indicado para o tratamento de pacientes adultos com mieloma múltiplo recidivante e / ou refratário que receberam pelo menos dois regimes anteriores, incluindo bortezomib e um agente imunomodulador.

Den Europæiske Union - portugisisk - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - lenalidomida - multiple myeloma; lymphoma, mantle-cell; myelodysplastic syndromes - imunossupressores - vários myelomarevlimid como monoterapia é indicado para o tratamento de manutenção de pacientes adultos diagnosticados com mieloma múltiplo que tenham sido submetidos a transplante de células-tronco autólogas. revlimid como a terapia de combinação com dexametasona, ou o bortezomib e dexametasona, ou melfalano e prednisona (ver secção 4,. 2) é indicado para o tratamento de pacientes adultos não tratados previamente com mieloma múltiplo que não são elegíveis para transplante. revlimid em combinação com dexametasona é indicado para o tratamento de mieloma múltiplo em pacientes adultos que receberam pelo menos uma terapêutica prévia. mielodisplásicas syndromesrevlimid como monoterapia é indicado para o tratamento de pacientes adultos com dependência de transfusões de anemia devido à baixa ou intermediária-1-risco de síndromes mielodisplásicas associado a um isolado de exclusão 5q anormalidade citogenética quando outras opções terapêuticas são insuficientes ou inadequadas. de células do manto lymphomarevlimid como monoterapia é indicado para o tratamento de pacientes adultos com recidivado ou refratário linfoma de células do manto. folicular lymphomarevlimid em combinação com rituximab (anti-cd20 de anticorpos) é indicado para o tratamento de doentes adultos tratados previamente folicular linfoma (grau 1 – 3a).

Den Europæiske Union - portugisisk - EMA (European Medicines Agency)

krka, d.d., novo mesto  - lenalidomide hydrochloride monohydrate - multiple myeloma; lymphoma, follicular - imunossupressores - multiple myelomalenalidomide krka d. novo mesto 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. novo mesto 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. novo mesto 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 krka d. novo mesto in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a). multiple myelomalenalidomide krka d. novo mesto 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. novo mesto 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. novo mesto 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 krka d. novo mesto in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a).

Den Europæiske Union - portugisisk - EMA (European Medicines Agency)

krka, d.d., novo mesto  - lenalidomide hydrochloride monohydrate - multiple myeloma; myelodysplastic syndromes; lymphoma, follicular; lymphoma, mantle-cell - imunossupressores - multiple myelomalenalidomide krka 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 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 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 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. mantle cell lymphomalenalidomide krka as monotherapy is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (see sections 4. 4 e 5. follicular lymphomalenalidomide krka in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a). multiple myelomalenalidomide krka 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 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 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 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. mantle cell lymphomalenalidomide krka as monotherapy is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (see sections 4. 4 e 5. follicular lymphomalenalidomide krka in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a).

Den Europæiske Union - portugisisk - EMA (European Medicines Agency)

accord healthcare s.l.u. - lenalidomida - mieloma múltiplo - imunossupressores - multiple myelomalenalidomide accord as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation. lenalidomide accord 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. a lenalidomida acordo, em combinação com dexametasona é indicado para o tratamento de mieloma múltiplo em pacientes adultos que receberam pelo menos uma terapêutica prévia. follicular lymphomalenalidomide accord in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a).