Европейски съюз - нидерландски - EMA (European Medicines Agency)

janssen-cilag international nv - ciltacabtagene autoleucel - multiple myeloma - 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.

Европейски съюз - нидерландски - EMA (European Medicines Agency)

aop orphan pharmaceuticals gmbh - sugammadex sodium - neuromusculaire blokkade - alle andere therapeutische producten - omkering van neuromusculaire blokkade geïnduceerd door rocuronium of vecuronium. for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.

Европейски съюз - нидерландски - EMA (European Medicines Agency)

janssen-cilag international n.v. - abiraterone acetate, niraparib tosilate monohydrate - de prostaat tumoren, castratie-resistente - antineoplastische middelen - treatment of adult patients with prostate cancer.

Европейски съюз - нидерландски - EMA (European Medicines Agency)

amgen technology (ireland) uc - eculizumab - hemoglobinurie, paroxysmale - immunosuppressiva - bekemv is indicated in adults and children for the treatment of paroxysmal nocturnal haemoglobinuria (pnh). bewijs van klinisch voordeel aangetoond bij patiënten met hemolyse met klinische symptomen(s) een indicatie van een hoge ziekte activiteit uitoefent, ongeacht transfusie geschiedenis (zie sectie 5.