Euroopa Liit - hispaania - EMA (European Medicines Agency)

holostem s.r.l - células epiteliales corneales humanas autólogas expandidas ex vivo que contienen células madre - stem cell transplantation; corneal diseases - oftalmológicos - tratamiento de pacientes adultos con moderada a severa límbica (definido por la presencia de neovascularización corneal superficial en al menos dos cuadrantes corneales, con afectación corneal central y deterioró severamente la agudeza visual), unilateral o bilateral, debido a las quemaduras oculares químicas o físicas. se requiere un mínimo de 1-2 mm2 de limbo no dañado para la biopsia.

Euroopa Liit - hispaania - EMA (European Medicines Agency)

teva b.v. - telmisartan - hipertensión - agentes que actúan sobre el sistema renina-angiotensina - el tratamiento de la hipertensión esencial en adultos.

Euroopa Liit - hispaania - EMA (European Medicines Agency)

takeda pharma a/s - alogliptin - diabetes mellitus, tipo 2 - drugs used in diabetes, dipeptidyl peptidase 4 (dpp-4) inhibitors - vipidia está indicado en adultos mayores de 18 años y mayores con diabetes mellitus tipo 2 para mejorar el control glucémico en combinación con otros medicamentos incluyendo insulina, cuando éstos, junto con dieta y ejercicio, no proporcionan suficiente hipoglucemiante el control glucémico (ver secciones 4. 4, 4. 5 y 5. 1 para datos disponibles sobre diferentes combinaciones).

Euroopa Liit - hispaania - EMA (European Medicines Agency)

novartis europharm limited  - onasemnogene abeparvovec - atrofia muscular, espinal - otras drogas para trastornos del sistema musculoesquelético - zolgensma está indicado para el tratamiento de pacientes con 5q de la atrofia muscular espinal (sma) con un bi-alélica de la mutación en el gen smn1 y el diagnóstico clínico de la atrofia muscular espinal tipo 1, orpatients con 5q sma con un bi-alélica de la mutación en el gen smn1 y hasta 3 copias del gen smn2.

Euroopa Liit - hispaania - EMA (European Medicines Agency)

gilead sciences ireland unlimited company - lenacapavir sodium - infecciones por vih - antivirales para uso sistémico - sunlenca injection, in combination with other antiretroviral(s), is indicated for the treatment of adults with multidrug resistant hiv 1 infection for whom it is otherwise not possible to construct a suppressive anti viral regimen (see sections 4. 2 y 5. sunlenca tablet, in combination with other antiretroviral(s), is indicated for the treatment of adults with multidrug resistant hiv 1 infection for whom it is otherwise not possible to construct a suppressive anti viral regimen, for oral loading prior to administration of long-acting lenacapavir injection (see sections 4. 2 y 5.

Euroopa Liit - hispaania - EMA (European Medicines Agency)

amgen europe b.v. - talimogene laherparepvec - melanoma - agentes antineoplásicos - imlygic está indicado para el tratamiento de adultos con melanoma irresecable que es metástasis regional o distante (etapa iiib, iiic y ivm1a) con la sin hueso, cerebro, pulmón u otra enfermedad visceral.

Euroopa Liit - hispaania - EMA (European Medicines Agency)

elanco gmbh - valnemulin - antiinfectives para uso sistémico - pigs; rabbits - pigsthe de prevención y tratamiento de la disentería porcina. el tratamiento de los signos clínicos de la enteropatía proliferativa porcina (ileítis). la prevención de los signos clínicos de la espiroquetosis colónica porcina (colitis) cuando la enfermedad ha sido diagnosticada en el rebaño. tratamiento y prevención de la neumonía enzoótica porcina. con la dosis recomendada de 10-12 mg / kg de peso corporal, las lesiones pulmonares y la pérdida de peso se reducen, pero la infección con mycoplasma hyopneumoniae no se elimina. rabbitsreduction de mortalidad durante un brote de epizoótica del conejo enteropatía (ere). el tratamiento debe iniciarse temprano en el brote, cuando el primer conejo ha sido diagnosticado con la enfermedad clínicamente.

Euroopa Liit - hispaania - 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.

Euroopa Liit - hispaania - EMA (European Medicines Agency)

moderna biotech spain, s.l. - single-stranded, 5’-capped messenger rna (mrna) 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 - spikevax is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older. spikevax bivalent original/omicron ba. 1 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 years of age and older who have previously received at least a primary vaccination course against covid-19. spikevax bivalent original/omicron ba. 4-5 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older.  spikevax xbb. 5 is indicated for active immunisation to prevent covid 19 caused by sars-cov-2 in individuals 6 months of age and older. the use of this vaccine should be in accordance with official recommendations.

Hispaania - hispaania - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

kern pharma s.l. - darunavir - comprimido recubierto con pelÍcula - 800 mg - darunavir 800 mg - darunavir