Франция - французский - ANSM (Agence Nationale de Sécurité du Médicament et des Produits de Santé)

laboratoires thea - cyanocobalamine 0 - collyre - 0,05 g - pour 100 ml de collyre > cyanocobalamine 0,05 g - medicament a usage ophtalmique/a visee cicatrisante - ce médicament est préconisé comme traitement d'appoint des troubles de la cicatrisation de l'œil.

Франция - французский - ANSM (Agence Nationale de Sécurité du Médicament et des Produits de Santé)

horus pharma - cyanocobalamine 0 - collyre - 0,050 g - pour 100 ml > cyanocobalamine 0,050 g - medicament ophtalmologique cicatrisant - ce médicament est préconisé comme traitement d'appoint des troubles de la cicatrisation cornéenne.

Франция - французский - ANSM (Agence Nationale de Sécurité du Médicament et des Produits de Santé)

substipharm - cyanocobalamine 250 - comprimé - 250,00 microgrammes - pour un comprimé > cyanocobalamine 250,00 microgrammes - antianemique - vitamine b12 - classe pharmacothérapeutique - code atc : antianemique - vitamine b12 - b03ba01.ce médicament contient de la vitamine b12.il est préconisé dans le traitement des anémies par carence d'apport alimentaire en vitamine b12 chez les végétaliens stricts depuis plus de 4 ans (régime alimentaire sans viande, laitages, œufs ou poisson) .

Франция - французский - ANSM (Agence Nationale de Sécurité du Médicament et des Produits de Santé)

laboratoires thea - cyanocobalamine 0 - collyre - 0,2 mg - pour 0,4 ml > cyanocobalamine 0,2 mg - ce médicament est préconisé comme traitement d'appoint des troubles de la cicatrisation oculaire.

Европейский союз - французский - EMA (European Medicines Agency)

amgen europe b.v. - adalimumab - arthritis, psoriatic; colitis, ulcerative; arthritis, juvenile rheumatoid; spondylitis, ankylosing; psoriasis; crohn disease; arthritis, rheumatoid - immunosuppresseurs - 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. le traitement de sévère, active et progressive de la polyarthrite rhumatoïde chez les adultes non précédemment traités par le méthotrexate. ,  amgevita can be given as monotherapy in case of intolerance to methotrexate or when continued treatment with methotrexate is inappropriate. amgevita réduit le taux de progression des lésions articulaires mesurés par radiographie et améliore la fonction physique, lorsqu'il est administré en association avec le méthotrexate. 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 peut être administré en monothérapie en cas d'intolérance au méthotrexate ou lorsque la poursuite du traitement avec le méthotrexate, est inadéquate (pour l'efficacité en monothérapie, voir la section 5. l'adalimumab n'a pas été étudié chez les patients âgés de moins de 2 ans. 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 réduit le taux de progression de l'atteinte articulaire périphérique tel que mesuré par rayons x dans les patients avec polyarticular symétrique sous-types de la maladie (voir la section 5. 1) et améliore la fonction physique. 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 et 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.

Европейский союз - французский - EMA (European Medicines Agency)

sandoz gmbh - adalimumab - arthritis, rheumatoid; arthritis, psoriatic; spondylitis, ankylosing; uveitis; hidradenitis suppurativa; colitis, ulcerative; arthritis, juvenile rheumatoid; crohn disease; skin diseases, papulosquamous - immunosuppresseurs - rheumatoid arthritishyrimoz 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. hyrimoz peut être administré en monothérapie en cas d'intolérance au méthotrexate ou lorsque la poursuite du traitement avec le méthotrexate est inapproprié. l'adalimumab a été montré pour réduire le taux de progression des lésions articulaires mesurés par radiographie et pour améliorer la fonction physique, lorsqu'il est administré en association avec le méthotrexate. juvenile idiopathic arthritis- polyarticular juvenile idiopathic arthritishyrimoz 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). hyrimoz peut être administré en monothérapie en cas d'intolérance au méthotrexate ou lorsque la poursuite du traitement avec le méthotrexate est inapproprié. l'adalimumab n'a pas été étudié chez les patients âgés de moins de 2 ans. - enthesitis-related arthritishyrimoz 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. axial spondyloarthritis- ankylosing spondylitis (as)hyrimoz 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 ashyrimoz 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 nonsteroidal anti-inflammatory drugs. psoriatic arthritishyrimoz 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. l'adalimumab a été montré pour réduire le taux de progression de l'atteinte articulaire périphérique tel que mesuré par rayons x dans les patients avec polyarticular symétrique sous-types de la maladie et pour améliorer la fonction physique. psoriasishyrimoz is indicated for the treatment of moderate to severe chronic plaque psoriasis in adult patients who are candidates for systemic therapy. paediatric plaque psoriasishyrimoz 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)hyrimoz 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. crohn’s diseasehyrimoz 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 diseasehyrimoz 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.  paediatric ulcerative colitishyrimoz 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. ulcerative colitishyrimoz 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. uveitishyrimoz 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 uveitishyrimoz 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.

Европейский союз - французский - EMA (European Medicines Agency)

eurocept international b. v. - acide para-aminosalicylique - tuberculose - antimycobactériens - granupas est indiquée dans le cadre d’un régime de combinaison appropriée pour une tuberculose multirésistante chez les adultes et les enfants de l’âge de 28 jours et plus âgés lorsqu’un schéma thérapeutique efficace ne peut pas être autrement composé pour des raisons de résistance ou la tolérance (voir la section 4. la considération devrait être donnée à des recommandations officielles concernant l'utilisation appropriée des antibactériens.

Бельгия - французский - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

viatris healthcare sa-nv - cyanocobalamine 0,5 mg; acide folique 0,8 mg; chlorhydrate de pyridoxine 3 mg - comprimé - 0,8 mg - 0,5 mg - 3 mg - cyanocobalamine 0.5 mg; acide folique 0.8 mg; chlorhydrate de pyridoxine 3 mg - vitamin b-complex, incl. combinations

Швейцария - французский - Swissmedic (Swiss Agency for Therapeutic Products)

medinova ag - zinci oxidum - cremepaste - zinci oxidum 200 mg, vaselinum album, paraffinum liquidum, alcohol cetylicus 55 mg, polysorbatum 60, sorbitani stearas, isopropylis myristas, decylis oleas, propylenglycolum 50 mg, e 307, butylis parahydroxybenzoas 0.4 mg, e 214 0.4 mg, e 218 3.2 mg, aqua purificata q.s. ad pastam pro 1 g. - l'érythème fessier, intertrigo, les petites blessures - synthetika

Европейский союз - французский - EMA (European Medicines Agency)

sanofi b.v. - eliglustat - maladie de gaucher - d'autres tractus digestif et le métabolisme des produits, - cerdelga est indiqué pour le traitement à long terme des patients adultes atteints de maladie de gaucher type 1 (gd1), qui sont pauvres cyp2d6 métaboliseurs (pms), métaboliseurs intermédiaires (ims) ou une vaste métaboliseurs (ems).