Brazīlija - portugāļu - ANVISA (Agência Nacional de Vigilância Sanitária)

fresenius kabi brasil ltda - adalimumabe - antinflamatorios antireumaticos

Eiropas Savienība - portugāļu - EMA (European Medicines Agency)

astrazeneca ab - tremelimumab - carcinoma, hepatocellular - agentes antineoplásicos - imjudo in combination with durvalumab is indicated for the first line treatment of adults with advanced or unresectable hepatocellular carcinoma (hcc). imjudo in combination with durvalumab and platinum-based chemotherapy is indicated for the first-line treatment of adults with metastatic non-small cell lung cancer (nsclc) with no sensitising egfr mutations or alk positive mutations.

Eiropas Savienība - portugāļu - EMA (European Medicines Agency)

astrazeneca ab - tremelimumab - carcinoma, pulmão de células não pequenas - agentes antineoplásicos - tremelimumab astrazeneca in combination with durvalumab and platinum-based chemotherapy is indicated for the first-line treatment of adults with metastatic non-small cell lung cancer (nsclc) with no sensitising egfr mutations or alk positive mutations.

Brazīlija - portugāļu - ANVISA (Agência Nacional de Vigilância Sanitária)

abbvie farmacÊutica ltda. - risanquizumabe - imunomodulador

Brazīlija - portugāļu - ANVISA (Agência Nacional de Vigilância Sanitária)

ucb biopharma ltda. - certolizumabe pegol - antinflamatorios

Eiropas Savienība - portugāļu - EMA (European Medicines Agency)

janssen-cilag international nv - guselkumab - psoríase - imunossupressores - plaque psoriasis tremfya is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. psoriatic arthritis tremfya, alone or in combination with methotrexate (mtx), is indicated for the treatment of active psoriatic arthritis in adult patients who have had an inadequate response or who have been intolerant to a prior disease-modifying antirheumatic drug (dmard) therapy (see section 5.

Eiropas Savienība - portugāļu - EMA (European Medicines Agency)

ucb pharma s.a.   - bimekizumab - psoríase - imunossupressores - plaque psoriasisbimzelx is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. psoriatic arthritisbimzelx, alone or in combination with methotrexate, is indicated for the treatment of active psoriatic arthritis in adults who have had an inadequate response or who have been intolerant to one or more disease-modifying antirheumatic drugs (dmards). axial spondyloarthritisnon-radiographic axial spondyloarthritis (nr-axspa)bimzelx is indicated for the treatment of adults with active non-radiographic axial spondyloarthritis with objective signs of inflammation as indicated by elevated c-reactive protein (crp) and/or magnetic resonance imaging (mri) who have responded inadequately or are intolerant to non-steroidal anti-inflammatory drugs (nsaids). ankylosing spondylitis (as, radiographic axial spondyloarthritis)bimzelx is indicated for the treatment of adults with active ankylosing spondylitis who have responded inadequately or are intolerant to conventional therapy.

Eiropas Savienība - portugāļu - EMA (European Medicines Agency)

hansa biopharma ab - imlifidase - desensitization, immunologic; kidney transplantation - imunossupressores - idefirix is indicated for desensitisation treatment of highly sensitised adult kidney transplant patients with positive crossmatch against an available deceased donor. the use of idefirix should be reserved for patients unlikely to be transplanted under the available kidney allocation system including prioritisation programmes for highly sensitised patients.

Brazīlija - portugāļu - ANVISA (Agência Nacional de Vigilância Sanitária)

bristol-myers squibb farmacÊutica ltda - abatacepte - antinflamatorios antireumaticos

Brazīlija - portugāļu - ANVISA (Agência Nacional de Vigilância Sanitária)

pfizer brasil ltda - citrato de tofacitinibe - imunosupressor