União Europeia -
português -
EMA (European Medicines Agency)
carvykti
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)
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.
União Europeia -
português -
EMA (European Medicines Agency)
sugammadex amomed
aop orphan pharmaceuticals gmbh - sugammadex sodium - bloqueio neuromuscular - todos os outros produtos terapêuticos - reversão do bloqueio neuromuscular induzido por rocurônio ou vecurônio. for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.
União Europeia -
português -
EMA (European Medicines Agency)
akeega
janssen-cilag international n.v. - abiraterone acetate, niraparib tosilate monohydrate - prostática benigna neoplasias, a castração-resistente - agentes antineoplásicos - treatment of adult patients with prostate cancer.
União Europeia -
português -
EMA (European Medicines Agency)
bekemv
amgen technology (ireland) uc - eculizumab - hemoglobinúria, paroxística - imunossupressores - bekemv is indicated in adults and children for the treatment of paroxysmal nocturnal haemoglobinuria (pnh). evidência de benefício clínico é demonstrado em pacientes com hemólise com sintoma clínico(s) indicativo de alta atividade de doença, independentemente de transfusão de história (consulte a secção 5.
União Europeia -
português -
EMA (European Medicines Agency)
talvey
janssen-cilag international n.v. - talquetamab - mieloma múltiplo - agentes antineoplásicos - talvey is indicated as monotherapy for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least 3 prior therapies, including an immunomodulatory agent, a proteasome inhibitor, and an anti cd38 antibody and have demonstrated disease progression on the last therapy.
