Europska Unija - španjolski - EMA (European Medicines Agency)

amgen europe b.v. - adalimumab - arthritis, psoriatic; colitis, ulcerative; arthritis, juvenile rheumatoid; spondylitis, ankylosing; psoriasis; crohn disease; arthritis, rheumatoid - inmunosupresores - rheumatoid arthritis  amgevita in combination with methotrexate, is indicated for: , the treatment of moderate to severe, active rheumatoid arthritis in adult patients when the response to disease-modifying anti-rheumatic drugs including methotrexate has been inadequate. el tratamiento de graves, activa y progresiva de la artritis reumatoide en adultos no tratados previamente con metotrexato. ,  amgevita can be given as monotherapy in case of intolerance to methotrexate or when continued treatment with methotrexate is inappropriate. amgevita reduce la tasa de progresión del daño articular medido por rayos x y de mejora de la función física, cuando se administra en combinación con metotrexato. juvenile idiopathic arthritis polyarticular juvenile idiopathic arthritis amgevita in combination with methotrexate is indicated for the treatment of active polyarticular juvenile idiopathic arthritis, in patients from the age of 2 years who have had an inadequate response to one or more disease-modifying anti-rheumatic drugs (dmards). amgevita puede ser administrado como monoterapia en caso de intolerancia al metotrexato o cuando el tratamiento continuado con metotrexato no es la adecuada (para la eficacia en monoterapia véase la sección 5. adalimumab no ha sido estudiado en pacientes menores de 2 años. enthesitis-related arthritis amgevita is indicated for the treatment of active enthesitis-related arthritis in patients, 6 years of age and older, who have had an inadequate response to, or who are intolerant of, conventional therapy (see section 5. axial spondyloarthritis ankylosing spondylitis (as) amgevita is indicated for the treatment of adults with severe active ankylosing spondylitis who have had an inadequate response to conventional therapy. axial spondyloarthritis without radiographic evidence of as amgevita is indicated for the treatment of adults with severe axial spondyloarthritis without radiographic evidence of as but with objective signs of inflammation by elevated crp and/or mri, who have had an inadequate response to, or are intolerant to non-steroidal anti-inflammatory drugs. psoriatic arthritis amgevita is indicated for the treatment of active and progressive psoriatic arthritis in adults when the response to previous disease-modifying anti-rheumatic drug therapy has been inadequate. amgevita reduce la tasa de progresión de periféricos daño articular medido por rayos x en pacientes con poliarticular simétrica subtipos de la enfermedad (ver sección 5. 1) y mejora la función física. psoriasis amgevita is indicated for the treatment of moderate to severe chronic plaque psoriasis in adult patients who are candidates for systemic therapy. paediatric plaque psoriasis amgevita is indicated for the treatment of severe chronic plaque psoriasis in children and adolescents from 4 years of age who have had an inadequate response to or are inappropriate candidates for topical therapy and phototherapies. hidradenitis suppurativa (hs) amgevita is indicated for the treatment of active moderate to severe hidradenitis suppurativa (acne inversa) in adults and adolescents from 12 years of age with an inadequate response to conventional systemic hs therapy (see sections 5. 1 y 5. crohn’s disease amgevita is indicated for treatment of moderately to severely active crohn’s disease, in adult patients who have not responded despite a full and adequate course of therapy with a corticosteroid and/or an immunosuppressant; or who are intolerant to or have medical contraindications for such therapies. paediatric crohn's disease amgevita is indicated for the treatment of moderately to severely active crohn's disease in paediatric patients (from 6 years of age) who have had an inadequate response to conventional therapy including primary nutrition therapy and a corticosteroid and/or an immunomodulator, or who are intolerant to or have contraindications for such therapies. ulcerative colitis amgevita is indicated for treatment of moderately to severely active ulcerative colitis in adult patients who have had an inadequate response to conventional therapy including corticosteroids and 6-mercaptopurine (6-mp) or azathioprine (aza), or who are intolerant to or have medical contraindications for such therapies. uveitis amgevita is indicated for the treatment of non-infectious intermediate, posterior and panuveitis in adult patients who have had an inadequate response to corticosteroids, in patients in need of corticosteroid-sparing, or in whom corticosteroid treatment is inappropriate. paediatric uveitis amgevita is indicated for the treatment of paediatric chronic non-infectious anterior uveitis in patients from 2 years of age who have had an inadequate response to or are intolerant to conventional therapy, or in whom conventional therapy is inappropriate.

Venezuela - španjolski - Instituto Nacional de Higiene

janssen cilag, c.a. - infliximab - polvo liofilizado para infusion - 100 mg

Europska Unija - španjolski - EMA (European Medicines Agency)

sandoz gmbh - infliximab - arthritis, psoriatic; psoriasis; crohn disease; arthritis, rheumatoid; colitis, ulcerative; spondylitis, ankylosing - inmunosupresores - tratamiento de la artritis reumatoide, enfermedad de crohn, la colitis ulcerosa, la espondilitis anquilosante, la artritis psoriásica y la psoriasis.

Europska Unija - španjolski - EMA (European Medicines Agency)

celltrion healthcare hungary kft. - adalimumab - arthritis, rheumatoid; arthritis, psoriatic; psoriasis; spondylitis, ankylosing; uveitis; hidradenitis suppurativa; colitis, ulcerative; crohn disease; arthritis, juvenile rheumatoid - inmunosupresores - rheumatoid arthritisyuflyma in combination with methotrexate, is indicated for:- the treatment of moderate to severe, active rheumatoid arthritis in adult patients when the response to disease-modifying anti-rheumatic drugs including methotrexate has been inadequate. - the treatment of severe, active and progressive rheumatoid arthritis in adults not previously treated with methotrexate. yuflyma can be given as monotherapy in case of intolerance to methotrexate or when continued treatment with methotrexate is inappropriate. adalimumab ha demostrado reducir la tasa de progresión del daño articular medido por rayos x y para mejorar la función física, cuando se administra en combinación con metotrexato. juvenile idiopathic arthritispolyarticular juvenile idiopathic arthritisyuflyma in combination with methotrexate is indicated for the treatment of active polyarticular juvenile idiopathic arthritis, in patients from the age of 2 years who have had an inadequate response to one or more disease-modifying anti-rheumatic drugs (dmards). yuflyma can be given as monotherapy in case of intolerance to methotrexate or when continued treatment with methotrexate is inappropriate (for the efficacy in monotherapy see section 5. adalimumab no ha sido estudiado en pacientes menores de 2 años. enthesitis-related arthritisyuflyma is indicated for the treatment of active enthesitis-related arthritis in patients, 6 years of age and older, who have had an inadequate response to, or who are intolerant of, conventional therapy (see section 5. axial spondyloarthritisankylosing spondylitis (as)yuflyma is indicated for the treatment of adults with severe active ankylosing spondylitis who have had an inadequate response to conventional therapy. axial spondyloarthritis without radiographic evidence of asyuflyma is indicated for the treatment of adults with severe axial spondyloarthritis without radiographic evidence of as but with objective signs of inflammation by elevated crp and/or mri, who have had an inadequate response to, or are intolerant to non-steroidal anti-inflammatory drugs (nsaids). psoriatic arthritisyuflyma is indicated for the treatment of active and progressive psoriatic arthritis in adults when the response to previous disease-modifying anti-rheumatic drug therapy has been inadequate. adalimumab ha demostrado reducir la tasa de progresión de periféricos daño articular medido por rayos x en pacientes con poliarticular simétrica subtipos de la enfermedad (ver sección 5. 1) y para mejorar la función física. psoriasisyuflyma is indicated for the treatment of moderate to severe chronic plaque psoriasis in adult patients who are candidates for systemic therapy. paediatric plaque psoriasisyuflyma is indicated for the treatment of severe chronic plaque psoriasis in children and adolescents from 4 years of age who have had an inadequate response to or are inappropriate candidates for topical therapy and phototherapies. hidradenitis suppurativa (hs)yuflyma is indicated for the treatment of active moderate to severe hidradenitis suppurativa (acne inversa) in adults and adolescents from 12 years of age with an inadequate response to conventional systemic hs therapy (see sections 5. 1 y 5. crohn’s diseaseyuflyma is indicated for treatment of moderately to severely active crohn’s disease, in adult patients who have not responded despite a full and adequate course of therapy with a corticosteroid and/or an immunosuppressant; or who are intolerant to or have medical contraindications for such therapies. paediatric crohn's diseaseyuflyma is indicated for the treatment of moderately to severely active crohn's disease in paediatric patients (from 6 years of age) who have had an inadequate response to conventional therapy including primary nutrition therapy and a corticosteroid and/or an immunomodulator, or who are intolerant to or have contraindications for such therapies. ulcerative colitisyuflyma is indicated for treatment of moderately to severely active ulcerative colitis in adult patients who have had an inadequate response to conventional therapy including corticosteroids and 6-mercaptopurine (6-mp) or azathioprine (aza), or who are intolerant to or have medical contraindications for such therapies. paediatric ulcerative colitisyuflyma is indicated for the treatment of moderately to severely active ulcerative colitis in paediatric patients (from 6 years of age) who have had an inadequate response to conventional therapy including corticosteroids and/or 6-mercaptopurine (6-mp) or azathioprine (aza), or who are intolerant to or have medical contraindications for such therapies. uveitisyuflyma is indicated for the treatment of non-infectious intermediate, posterior and panuveitis in adult patients who have had an inadequate response to corticosteroids, in patients in need of corticosteroid- sparing, or in whom corticosteroid treatment is inappropriate. paediatric uveitisyuflyma is indicated for the treatment of paediatric chronic non-infectious anterior uveitis in patients from 2 years of age who have had an inadequate response to or are intolerant to conventional therapy, or in whom conventional therapy is inappropriate.

Čile - španjolski - ISPC (Instituto de Salud Pública de Chile)

laboratorios wyeth llc. - etanercept - sin formulas

Čile - španjolski - ISPC (Instituto de Salud Pública de Chile)

abbvie productos farmacÉuticos ltda. - adalimumab - adalimumab* 40,0 mg - adultos: - artritis reumatoidea humira se indica para reducir los signos y síntomas, incluyendo mejoría en la respuesta clínica y remisión clínica inhibiendo la progresión del daño estructural y mejorando la función física en pacientes adultos con artritis reumatoidea moderada a severamente activa (ar). humira ha mostrado reducir la tasa de progresión del daño articular medido por rayos x y mejora la función física cuando se administra conjuntamente con metotrexato. humira se puede utilizar solo o en combinación con metotrexato u otras drogas antirreumáticas modificadoras de enfermedad (dmards). -artritis psoriática humira se indica para reducir los signos y síntomas de artritis activa en pacientes con artritis psoriática (aps). humira ha mostrado que reduce la tasa de progresión de daño articular periférico estructural y mejora la función física. humira se puede utilizar solo o en combinación con dmards. -espondiloartritis axial espondilitis anquilosante humira se indica para reducir los signos y síntomas en pacientes con espondilitis anquilosante (ea) activa que tienen una respuesta inadecuada a la terapia convencional. espondiloartritis axial no-radiográfica (espondiloartritis axial sin evidencia radiográfica de ea) humira se indica para reducir los signos y síntomas en pacientes con espondiloartritis axial no-radiográfica (spanrax) activa, pero con signos objetivos de inflamación por elevación de la pcr y/o resonancia magnética, que han tenido una respuesta inadecuada a, o son intolerantes a anti-inflamatorios no esteroidales. -enfermedad de crohn humira se indica para reducir los signos y síntomas, e inducir y mantener la remisión clínica en pacientes adultos con enfermedad de crohn (ec) moderada a severamente activa que han tenido una respuesta inadecuada a la terapia convencional. humira se indica para reducir los signos y síntomas e inducir remisión clínica en estos pacientes si ellos también han perdido respuesta a o son intolerantes a infliximab. -colitis ulcerosa humira se indica para el tratamiento de colitis ulcerosa (cu) moderada a severamente activa en pacientes adultos que han tenido una respuesta inadecuada a la terapia convencional incluyendo corticosteroides y/o 6-mercaptopurina (6-mp) o azatioprina (aza), o que son intolerantes a o tienen contraindicaciones médicas para tales terapias. -psoriasis en placa humira se indica para el tratamiento de pacientes adultos con psoriasis crónica en placa moderada a severa que son candidatos a terapia sistémica o fototerapia y cuando otras terapias sistémicas son médicamente menos apropiadas. -hidradenitis supurativa humira está indicado para el tratamiento de pacientes adultos con hidradenitis supurativa (acné inversa), de moderada a severa, incluyendo el tratamiento de lesiones inflamatorias y la prevención del empeoramiento de abscesos y fístulas drenantes. -uveítis humira está indicado para el tratamiento de uveítis no infecciosa anterior, intermediaria, posterior y panuveitis en pacientes adultos. pacientes pediátricos artritis idiopática juvenil artritis idiopática juvenil poliarticular humira se indica para reducir los signos y síntomas de la artritis idiopática juvenil poliarticular (aijp) moderada a severamente activa en pacientes desde los 13 años de edad. humira se puede usar solo o en combinación con metotrexato humira se indica para el tratamiento de pacientes adultos con psoriasis crónica en placa moderada a severa que son candidatos a terapia sistémica o fototerapia. humira está indicado para psoriasis de uñas de moderada a severa en pacientes adultos que son candidatos a terapia sistémica. artritis idiopática juvenil poliarticular humira en combinación con metotrexato está indicada para el tratamiento de la artritis idiopática juvenil poliarticular activa en niños y adolescentes a partir de 2 años que han presentado una respuesta insuficiente a uno o más fármacos antirreumáticos modificadores de ia enfermedad (dmards). humira puede ser administrado en monoterapia en caso de intolerancia al metotrexato o cuando el tratamiento continuado con metotrexato no sea posible. no se ha estudiado el uso de humira en niños menores de 2 años. artritis relacionada con entesitis humira está indicado para el tratamiento de artritis relacionada con entesitis, en pacientes de 6 años de edad y mayores, que han tenido una respuesta inadecuada, o que son intolerantes a la terapia convencional. enfermedad de crohn pediátrico humira está indicado para el tratamiento de la enfermedad de crohn activa de moderada a severa, en pacientes pediátricos (a partir de los 6 años de edad) que han presentado una respuesta insuficiente a ia terapia convencional incluyendo tratamiento nutricional primario, un corticoesteroide, y un inmunomodulador, o que son intolerantes o tienen contraindicadas estas terapias. psoriasis en placa en pediatría humira está indicado para el tratamiento de pacientes con psoriasis en placa crónica y severa, en niños y adolescentes a partir de los 4 años de edad que han tenido una respuesta inadecuada o que son candidatos inapropiados para terapia tópica o fototerapia. hidradenitis suporativa en adolecentes humira está indicado en el tratamientos de hidradenitis supurativa activa (acné inverso) moderada a severa en adolecentes desde 12 años de edad con una inadecuada respuesta a la terapia convencional para hidradenitis supurativa ( hs). uveitis pediátrica humira está indicado para el tratamiento de uveitis crónica no infecciosa en pacientes pediátricos de 2 años de edad y mayores.

Čile - španjolski - ISPC (Instituto de Salud Pública de Chile)

abbvie productos farmacÉuticos ltda. - adalimumab - sin formulas

Peru - španjolski - DIGEMID (Dirección General de Medicamentos, Insumos y Drogas)

pfizer s.a. - droguerÍa - adalimumab - solucion inyectable - 40mg/0.8m - por mililitro - - adalimumab