Unión Europea - español - EMA (European Medicines Agency)

aimmune therapeutics ireland limited - defatted powder of arachis hypogaea l., semen (peanuts) - peanut hypersensitivity - allergens - palforzia is indicated for the treatment of patients aged 4 to 17 years with a confirmed diagnosis of peanut allergy. palforzia may be continued in patients 18 years of age and older. palforzia should be used in conjunction with a peanut-avoidant diet.

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

fatro s.p.a. - acido 2-fenoxi-2-metilpropionico - soluciÓn inyectable - acido 2-fenoxi-2-metilpropionico 100mg - terapia hepática - bovino; caprino; caballos; porcino; perros

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

byk leo, s.l. - timonacato arginina - excipientes: - terapia hepÁtica, lipotrÓpicos - terapia hepática -

Unión Europea - español - EMA (European Medicines Agency)

ptc therapeutics international limited - eladocagene exuparvovec - metabolismo de aminoácidos, errores congénitos - enzymes, other alimentary tract and metabolism products - upstaza is indicated for the treatment of patients aged 18 months and older with a clinical, molecular, and genetically confirmed diagnosis of aromatic l amino acid decarboxylase (aadc) deficiency with a severe phenotype (see section 5.

Unión Europea - español - EMA (European Medicines Agency)

amicus therapeutics europe limited - miglustat - enfermedad de almacenamiento de glucógeno tipo ii - otros productos del metabolismo y del tracto alimentario - opfolda (miglustat) is an enzyme stabiliser of cipaglucosidase alfa long-term enzyme replacement therapy in adults with late-onset pompe disease (acid α- glucosidase [gaa] deficiency).

Unión Europea - español - EMA (European Medicines Agency)

glaxosmithkline biologicals s.a.  - respiratory syncytial virus recombinant glycoprotein f stabilised in the pre-fusion conformation (rsvpref3) produced in chinese hamster ovary (cho) cells by recombinant dna technology - infecciones por virus sincicial respiratorio - vacunas - arexvy is indicated for active immunisation for the prevention of lower respiratory tract disease (lrtd) caused by respiratory syncytial virus in adults 60 years of age and older. el uso de esta vacuna debe estar en conformidad con las recomendaciones oficiales.

Unión Europea - español - EMA (European Medicines Agency)

immunocore ireland limited - tebentafusp - uveal neoplasms - agentes antineoplásicos - kimmtrak is indicated as monotherapy for the treatment of human leukocyte antigen (hla)-a*02:01-positive adult patients with unresectable or metastatic uveal melanoma.

Unión Europea - español - EMA (European Medicines Agency)

biogen netherlands b.v. - fumarato de dimetilo - esclerosis múltiple - inmunosupresores - tecfidera is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).

Unión Europea - español - EMA (European Medicines Agency)

biogen netherlands b.v. - natalizumab - esclerosis múltiple - inmunosupresores selectivos - tysabri is indicated as single disease modifying therapy in adults with highly active relapsing remitting multiple sclerosis for the following patient groups: , patients with highly active disease activity despite a full and adequate course of treatment with at least one disease modifying therapy (dmt) (for exceptions and information about washout periods see sections 4. 4 y 5. 1), , or, patients with rapidly evolving severe relapsing remitting multiple sclerosis defined by 2 or more disabling relapses in one year, and with 1 or more gadolinium enhancing lesions on brain mri or a significant increase in t2 lesion load as compared to a previous recent mri.

Unión Europea - español - EMA (European Medicines Agency)

blueprint medicines (netherlands) b.v. - avapritinib - tumores del estroma gastrointestinal - otros agentes antineoplásicos, inhibidores de la proteína quinasa - ayvakyt is indicated as monotherapy for the treatment of adult patients with unresectable or metastatic gastrointestinal stromal tumours (gist) harbouring the platelet-derived growth factor receptor alpha (pdgfra) d842v mutation.