Liên Minh Châu Âu - Tiếng Tây Ban Nha - EMA (European Medicines Agency)

eisai gmbh - bexaroteno - linfoma, t-cell, cutáneo - agentes antineoplásicos - las cápsulas de targretin están indicadas para el tratamiento de las manifestaciones cutáneas de los pacientes con linfoma cutáneo de células t en estadio avanzado (ctcl) refractarios a al menos un tratamiento sistémico.

Liên Minh Châu Âu - Tiếng Tây Ban Nha - EMA (European Medicines Agency)

ceft biopharma s.r.o. - ibritumomab tiuxetan - linfoma, folicular - radiofármacos terapéuticos - zevalin está indicado en adultos. [90y]-radiomarcados zevalin está indicado como terapia de consolidación después de la inducción de la remisión en pacientes no tratados previamente con linfoma folicular. el beneficio de zevalin siguientes rituximab en combinación con quimioterapia no ha sido establecida. [90y]-radiomarcados zevalin está indicado para el tratamiento de pacientes adultos con rituximab relapsedorrefractory cd20+ folicular de células b linfoma no-hodgkin (lnh).

Liên Minh Châu Âu - Tiếng Tây Ban Nha - EMA (European Medicines Agency)

novartis europharm limited  - siponimod el ácido fumárico - la esclerosis múltiple remitente-recurrente - inmunosupresores selectivos - mayzent está indicado para el tratamiento de pacientes adultos con esclerosis múltiple secundaria progresiva (emsp) con enfermedad activa se evidencia por recaídas o características de las imágenes de la actividad inflamatoria.

Liên Minh Châu Âu - Tiếng Tây Ban Nha - EMA (European Medicines Agency)

accord healthcare s.l.u. - fingolimod clorhidrato de - la esclerosis múltiple remitente-recurrente - los inmunosupresores selectivos de inmunosupresores - indicado como único modificadores de la enfermedad la terapia altamente activa la esclerosis múltiple remitente recidivante para los siguientes grupos de pacientes adultos y pacientes pediátricos de 10 años de edad y mayores:los pacientes con muy activa de la enfermedad a pesar de una completa y adecuada curso de tratamiento con al menos uno de los modificadores de la enfermedad therapyorpatients con la rapidez de la evolución grave de la esclerosis múltiple remitente recidivante definido por 2 o más incapacitante de recaídas en un año, y con 1 o más gadolinio mejora de las lesiones en la rm cerebral o un aumento significativo de la carga lesional en t2 como en comparación con anteriores reciente resonancia magnética.

Liên Minh Châu Âu - Tiếng Tây Ban Nha - EMA (European Medicines Agency)

biontech manufacturing gmbh - single-stranded, 5’-capped messenger rna produced using a cell-free in vitro transcription from the corresponding dna templates, encoding the viral spike (s) protein of sars-cov-2 - covid-19 virus infection - vacunas - comirnaty 30 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty original/omicron ba. 1 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older who have previously received at least a primary vaccination course against covid-19. comirnaty original/omicron ba. 4-5 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty original/omicron ba. 4-5 (1. 5/1. 5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty omicron xbb. 5 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty omicron xbb. 5 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 10 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years. el uso de esta vacuna debe estar en conformidad con las recomendaciones oficiales.

Liên Minh Châu Âu - Tiếng Tây Ban Nha - EMA (European Medicines Agency)

stemline therapeutics b.v. - tagraxofusp - lymphoma - agentes antineoplásicos - elzonris is indicated as monotherapy for the first-line treatment of adult patients with blastic plasmacytoid dendritic cell neoplasm (bpdcn).

Liên Minh Châu Âu - Tiếng Tây Ban Nha - 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.

Liên Minh Châu Âu - Tiếng Tây Ban Nha - EMA (European Medicines Agency)

astrazeneca ab - chadox1-sars-cov-2 - covid-19 virus infection - vacunas - vaxzevria 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.

Liên Minh Châu Âu - Tiếng Tây Ban Nha - EMA (European Medicines Agency)

mylan ireland limited - fingolimod clorhidrato de - la esclerosis múltiple remitente-recurrente - inmunosupresores - indicated as single disease modifying therapy in highly active relapsing remitting multiple sclerosis for the following groups of adult and paediatric patients aged 10 years and older:patients with highly active disease despite a full and adequate course of treatment with at least one disease modifying therapy (for exceptions and information about washout periods see sections 4. 4 y 5. 1)orpatients con la rapidez de la evolución grave de la esclerosis múltiple remitente recidivante definido por 2 o más incapacitante de recaídas en un año, y con 1 o más gadolinio mejora de las lesiones en la rm cerebral o un aumento significativo de la carga lesional en t2 como en comparación con anteriores reciente resonancia magnética.

Liên Minh Châu Âu - Tiếng Tây Ban Nha - EMA (European Medicines Agency)

intervacc ab - recombinant streptococcus equi protein cce, recombinant streptococcus equi protein eq85, recombinant streptococcus equi protein idee - inmunológicos para équidos - caballos - for the active immunisation to reduce clinical signs and the number of abscesses in acute stage of infection with s. equi.