Unión Europea - español - EMA (European Medicines Agency)

pfizer europe ma eeig  - voxelotor - anemia; anemia, hemolytic; anemia, sickle cell - other hematological agents - oxbryta is indicated for the treatment of haemolytic anaemia due to sickle cell disease (scd) in adults and paediatric patients 12 years of age and older as monotherapy or in combination with hydroxycarbamide.

Unión Europea - español - EMA (European Medicines Agency)

pfizer europe ma eeig - pneumococcal polysaccharide serotype 1, pneumococcal polysaccharide serotype 3, pneumococcal polysaccharide serotype 4, pneumococcal polysaccharide serotype 5, pneumococcal polysaccharide serotype 6a, pneumococcal polysaccharide serotype 6b, pneumococcal polysaccharide serotype 7f, pneumococcal polysaccharide serotype 8, pneumococcal polysaccharide serotype 9v, pneumococcal polysaccharide serotype 10a, pneumococcal polysaccharide serotype 11a, pneumococcal polysaccharide serotype 12f, pneumococcal polysaccharide serotype 14, pneumococcal polysaccharide serotype 15b, pneumococcal polysaccharide serotype 18c, pneumococcal polysaccharide serotype 19a, pneumococcal polysaccharide serotype 19f, pneumococcal polysaccharide serotype 22f, pneumococcal polysaccharide serotype 23f, pneumococcal polysaccharide serotype 33f - infecciones neumocócicas - vacunas - active immunisation for the prevention of invasive disease and pneumonia caused by streptococcus pneumoniae in individuals 18 years of age and older. ver secciones 4. 4 y 5. 1 para obtener información sobre la protección contra serotipos neumocócicos específicos. apexxnar should be used in accordance with official recommendations. .

Unión Europea - español - EMA (European Medicines Agency)

pfizer europe ma eeig  - tanezumab - osteoarthritis; pain - analgésicos - treatment of moderate to severe chronic pain associated with osteoarthritis (oa) of the hip or knee in adult patients for whom treatment with non-steroidal anti-inflammatory drugs (nsaids) and/or any opioid is ineffective, not tolerated or inappropriate.

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

pfizer europe ma eeig - eplerenona - excipientes: lactosa monohidrato,croscarmelosa sodica,laurilsulfato de sodio,polisorbato 80 - agentes ahorradores de potasio - antagonistas de la aldosterona - eplerenona

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

pfizer europe ma eeig - eplerenona - excipientes: lactosa monohidrato,croscarmelosa sodica,laurilsulfato de sodio,polisorbato 80 - agentes ahorradores de potasio - antagonistas de la aldosterona - eplerenona

Unión Europea - español - EMA (European Medicines Agency)

pfizer europe ma eeig - neisseria meningitidis serogrupo b fhbp (recombinante liphidrato fhbp (proteína de unión a factor h)) subfamilia a; neisseria meningitidis serogrupo b fhbp (recombinante liphidrato fhbp (proteína de unión a factor h)) subfamilia b - meningitis, meningocócica - bacterial vaccines, meningococcal vaccines - trumenba está indicado para la inmunización activa de individuos de 10 años o más para prevenir la enfermedad meningocócica invasiva causada por neisseria meningitidis serogrupo b. el uso de esta vacuna debe estar en conformidad con las recomendaciones oficiales.

Unión Europea - español - EMA (European Medicines Agency)

pfizer europe ma eeig - nonacog alfa - hemofilia b - antihemorrágicos - tratamiento y profilaxis de hemorragias en pacientes con hemofilia b (deficiencia congénita de factor ix).

Unión Europea - español - EMA (European Medicines Agency)

pfizer europe ma eeig - moroctocog alfa - hemofilia a - antihemorrágicos - tratamiento y profilaxis de hemorragias en pacientes con hemofilia a (deficiencia congénita de factor viii). refacto af es apropiado para su uso en adultos y niños de todas las edades, incluyendo los recién nacidos. refacto af no contiene von-willebrand factor, y por lo tanto no está indicado en von-willebrand la enfermedad de.

Unión Europea - español - EMA (European Medicines Agency)

pfizer europe ma eeig - tofacitinib - artritis, reumatoide - inmunosupresores - rheumatoid arthritistofacitinib in combination with methotrexate (mtx) is indicated for the treatment of moderate to severe active rheumatoid arthritis (ra) in adult patients who have responded inadequately to, or who are intolerant to one or more disease-modifying antirheumatic drugs (dmards) (see section 5. tofacitinib can be given as monotherapy in case of intolerance to mtx or when treatment with mtx is inappropriate (see sections 4. 4 y 4. psoriatic arthritistofacitinib in combination with mtx is indicated for the treatment of active psoriatic arthritis (psa) in adult patients who have had an inadequate response or who have been intolerant to a prior disease modifying antirheumatic drug (dmard) therapy (see section 5. ulcerative colitistofacitinib is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis (uc) who have had an inadequate response, lost response, or were intolerant to either conventional therapy or a biologic agent (see section 5. tofacitinib is indicated for the treatment of active polyarticular juvenile idiopathic arthritis (rheumatoid factor positive [rf+] or negative [rf-] polyarthritis and extended oligoarthritis), and juvenile psoriatic arthritis (psa) in patients 2 years of age and older, who have responded inadequately to previous therapy with disease modifying antirheumatic drugs (dmards). tofacitinib can be given in combination with methotrexate (mtx) or as monotherapy in case of intolerance to mtx or where continued treatment with mtx is inappropriate. ankylosing spondylitistofacitinib is indicated for the treatment of adult patients with active ankylosing spondylitis (as) who have responded inadequately to conventional therapy.

Unión Europea - español - EMA (European Medicines Agency)

pfizer europe ma eeig  - rimegepant - trastornos de la migraña - antimigraine preparations, calcitonin gene-related peptide (cgrp) antagonists - vydura is indicated for theacute treatment of migraine with or without aura in adults;preventative treatment of episodic migraine in adults who have at least 4 migraine attacks per month.