España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

laboratorios normon s.a. - fingolimod hidrocloruro - cÁpsula dura - 0,5 mg - fingolimod hidrocloruro 0,5 mg - fingolimod

España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

zentiva k.s. - fingolimod hidrocloruro - cÁpsula dura - 0,5 mg - fingolimod hidrocloruro 0,5 mg - fingolimod

España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

glenmark arzneimittel gmbh - fingolimod hidrocloruro - cÁpsula dura - 0,5 mg - fingolimod hidrocloruro 0,5 mg - fingolimod

Unión Europea - español - EMA (European Medicines Agency)

ucb pharma s.a.   - bimekizumab - psoriasis - inmunosupresores - plaque psoriasisbimzelx is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. psoriatic arthritisbimzelx, alone or in combination with methotrexate, is indicated for the treatment of active psoriatic arthritis in adults who have had an inadequate response or who have been intolerant to one or more disease-modifying antirheumatic drugs (dmards). axial spondyloarthritisnon-radiographic axial spondyloarthritis (nr-axspa)bimzelx is indicated for the treatment of adults with active non-radiographic axial spondyloarthritis with objective signs of inflammation as indicated by elevated c-reactive protein (crp) and/or magnetic resonance imaging (mri) who have responded inadequately or are intolerant to non-steroidal anti-inflammatory drugs (nsaids). ankylosing spondylitis (as, radiographic axial spondyloarthritis)bimzelx is indicated for the treatment of adults with active ankylosing spondylitis who have responded inadequately or are intolerant to conventional therapy.

Unión Europea - español - EMA (European Medicines Agency)

hansa biopharma ab - imlifidase - desensitization, immunologic; kidney transplantation - inmunosupresores - idefirix is indicated for desensitisation treatment of highly sensitised adult kidney transplant patients with positive crossmatch against an available deceased donor. the use of idefirix should be reserved for patients unlikely to be transplanted under the available kidney allocation system including prioritisation programmes for highly sensitised patients.

España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

products and technology s.l. - hidroxicloroquina sulfato - comprimido recubierto - 200 mg - hidroxicloroquina sulfato 200 mg - hidroxicloroquina

Unión Europea - español - EMA (European Medicines Agency)

takeda pharma a/s - vedolizumab - colitis, ulcerative; crohn disease - inmunosupresores selectivos - la colitis colitisentyvio está indicado para el tratamiento de pacientes adultos con moderada a gravemente activa la colitis ulcerosa que han tenido una respuesta inadecuada, perdió respuesta a, o eran intolerantes a la terapia convencional o un factor de necrosis tumoral alfa (tnfa), antagonista de la. la enfermedad de crohn diseaseentyvio está indicado para el tratamiento de pacientes adultos con moderada a gravemente activa la enfermedad de crohn que han tenido una respuesta inadecuada, perdió respuesta a, o eran intolerantes a la terapia convencional o un factor de necrosis tumoral alfa (tnfa), antagonista de la. pouchitisentyvio is indicated for the treatment of adult patients with moderately to severely active chronic pouchitis, who have undergone proctocolectomy and ileal pouch anal anastomosis for ulcerative colitis, and have had an inadequate response with or lost response to antibiotic therapy.

Unión Europea - español - EMA (European Medicines Agency)

mylan ireland limited - fumarato de dimetilo - la esclerosis múltiple remitente-recurrente - inmunosupresores - dimethyl fumarate mylan is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Unión Europea - español - EMA (European Medicines Agency)

zaklady farmafarmaceutyczne polpharma s.aceutyczne polpharma s.a. - fumarato de dimetilo - la esclerosis múltiple remitente-recurrente - inmunosupresores - dimethyl fumarate polpharma is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Unión Europea - español - EMA (European Medicines Agency)

teva gmbh - fumarato de dimetilo - multiple sclerosis, relapsing-remitting; multiple sclerosis - inmunosupresores - dimethyl fumarate teva is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).