Europos Sąjunga - ispanų - EMA (European Medicines Agency)

janssen-cilag international nv - rilpivirine - infecciones por vih - antivirales para uso sistémico - rekambys is indicated, in combination with cabotegravir injection, for the treatment of human immunodeficiency virus type 1 (hiv 1) infection in adults who are virologically suppressed (hiv-1 rna < 50 copies/ml) on a stable antiretroviral regimen without present or past evidence of viral resistance to, and no prior virological failure with, agents of the nnrti and ini class.

Europos Sąjunga - ispanų - EMA (European Medicines Agency)

janssen-cilag international nv - adenovirus type 26 encoding the sars-cov-2 spike glycoprotein (ad26.cov2-s) - covid-19 virus infection - vacunas - jcovden is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 18 years of age and older. el uso de esta vacuna debe estar en conformidad con las recomendaciones oficiales.

Europos Sąjunga - ispanų - EMA (European Medicines Agency)

janssen-cilag international n.v.    - amivantamab - carcinoma, pulmón no microcítico - agentes antineoplásicos - rybrevant as monotherapy is indicated for treatment of adult patients with locally advanced or metastatic non-small cell lung cancer (nsclc) with activating epidermal growth factor receptor (egfr) exon 20 insertion mutations, after failure of platinum-based chemotherapy.

Europos Sąjunga - ispanų - EMA (European Medicines Agency)

amgen europe bv - sotorasib - carcinoma, pulmón no microcítico - agentes antineoplásicos - lumykras as monotherapy is indicated for the treatment of adults with advanced non-small cell lung cancer (nsclc) with kras g12c mutation and who have progressed after at least one prior line of systemic therapy.

Europos Sąjunga - ispanų - EMA (European Medicines Agency)

janssen-cilag international nv - ciltacabtagene autoleucel - mieloma múltiple - 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.

Europos Sąjunga - ispanų - EMA (European Medicines Agency)

aop orphan pharmaceuticals gmbh - sugammadex sodium - bloqueo neuromuscular - todos los demás productos terapéuticos - reversión del bloqueo neuromuscular inducido por rocuronio o vecuronio. for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.

Europos Sąjunga - ispanų - EMA (European Medicines Agency)

janssen-cilag international n.v. - abiraterone acetate, niraparib tosilate monohydrate - próstata neoplasias, resistente a la castración - agentes antineoplásicos - treatment of adult patients with prostate cancer.

Europos Sąjunga - ispanų - EMA (European Medicines Agency)

amgen technology (ireland) uc - eculizumab - hemoglobinuria, paroxística - inmunosupresores - bekemv is indicated in adults and children for the treatment of paroxysmal nocturnal haemoglobinuria (pnh). evidencia de beneficio clínico se ha demostrado en pacientes con hemólisis con síntoma clínico(s) indicativo de la alta actividad de la enfermedad, independientemente de los antecedentes de transfusión (véase la sección 5.