Europäische Union - Deutsch - EMA (European Medicines Agency)

olympus biotech international limited - eptotermin alfa - spondylolisthesis - medikamente zur behandlung von knochenerkrankungen - opgenra ist indiziert für die posterolaterale lumbale spinalfusion bei erwachsenen patienten mit spondylolisthese, bei denen das autotransplantat versagt hat oder kontraindiziert ist.

Europäische Union - Deutsch - EMA (European Medicines Agency)

abbvie deutschland gmbh & co. kg - dexamethason - macular edema; uveitis - ophthalmologicals, other ophthalmologicals - ozurdex ist indiziert für die behandlung von erwachsenen patienten mit makula-ödem nach entweder branch retinal-vein occlusion (vav) oder central-retinal-vein occlusion (crvo). ozurdex ist indiziert für die behandlung von erwachsenen patienten mit einer entzündung des posterioren segments des auges, die vorlage als nichtinfektiöse uveitis. ozurdex ist indiziert für die behandlung von erwachsenen patienten mit sehbehinderungen durch diabetische makula-ödem (dme), die pseudophaken oder als unzureichend zu reagieren, oder ungeeignet für nicht-kortikosteroid-therapie.

Deutschland - Deutsch - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

baxter oncology gmbh (8044474) - cyclophosphamid 1 h<2>o - überzogene tablette - teil 1 - überzogene tablette; cyclophosphamid 1 h<2>o (12932) 53,5 milligramm

Europäische Union - Deutsch - EMA (European Medicines Agency)

astellas pharma europe b.v. - gilteritinib fumarate - leukämie, myeloisch, akut - antineoplastische mittel - xospata ist indiziert als monotherapie für die behandlung erwachsener patienten mit rezidivierter oder refraktärer akuter myeloischer leukämie (aml) mit flt3-mutation.

Österreich - Deutsch - AGES (Agentur für Gesundheit und Ernährungssicherheit)

koanaa healthcare spain - gemcitabin hydrochlorid -

Europäische Union - Deutsch - 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 - immunsuppressiva - 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 wurde gezeigt, zur verringerung der rate des fortschreitens von gelenkschäden, wie gemessen, durch die x-ray und für die verbesserung der physischen funktion, wenn sie in kombination mit methotrexat. 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 wurde nicht untersucht bei patienten im alter von weniger als 2 jahren. 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 wurde gezeigt, zur verringerung der rate des fortschreitens peripherer gelenkschäden, wie gemessen, durch die x-ray bei patienten mit polyarticular symmetrischen subtypen der erkrankung (siehe abschnitt 5. 1) und auf die verbesserung der physischen funktion. 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 und 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.

Deutschland - Deutsch - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

wala-heilmittel gmbh (3092764) - plexus gastricus bovis (pot.-angaben) - flüssige verdünnung zur injektion - plexus gastricus bovis (pot.-angaben) (16514) information nicht vorhanden

Deutschland - Deutsch - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

betapharm arzneimittel gmbh (3364323) - fingolimodhydrochlorid - hartkapsel - 0,5 mg - teil 1 - hartkapsel; fingolimodhydrochlorid (30117) 0,56 milligramm

Österreich - Deutsch - AGES (Agentur für Gesundheit und Ernährungssicherheit)

grifols deutschland gmbh - immunglobulin - immunglobuline, normal

Deutschland - Deutsch - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

sanofi pasteur europe (4609086) - tollwut-virus, stamm wistar pm/wi 38-1503-3m, inaktiviert - lyophilisat und lösungsmittel zur herstellung einer injektionssuspension - tollwut-virus, stamm wistar pm/wi 38-1503-3m, inaktiviert (31433) 2,5 internationale einheit