België - Nederlands - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

lundbeck sa-nv - amitriptylinehydrochloride 28,28 mg - eq. amitriptyline 25 mg - filmomhulde tablet - 25 mg - amitriptylinehydrochloride 28.28 mg - amitriptyline

Europese Unie - Nederlands - EMA (European Medicines Agency)

abbvie deutschland gmbh & co. kg - upadacitinib - artritis, reumatoïde - immunosuppressiva - rheumatoid arthritisrinvoq is indicated for the treatment of moderate to severe active rheumatoid arthritis in adult patients who have responded inadequately to, or who are intolerant to one or more disease-modifying anti-rheumatic drugs (dmards). rinvoq may be used as monotherapy or in combination with methotrexate. psoriatic arthritisrinvoq is indicated for the treatment of active psoriatic arthritis in adult patients who have responded inadequately to, or who are intolerant to one or more dmards. rinvoq may be used as monotherapy or in combination with methotrexate. axial spondyloarthritisnon-radiographic axial spondyloarthritis (nr-axspa)rinvoq is indicated for the treatment of active non-radiographic axial spondyloarthritis in adult patients with objective signs of inflammation as indicated by elevated c-reactive protein (crp) and/or magnetic resonance imaging (mri), who have responded inadequately to nonsteroidal anti-inflammatory drugs (nsaids). ankylosing spondylitis (as, radiographic axial spondyloarthritis)rinvoq is indicated for the treatment of active ankylosing spondylitis in adult patients who have responded inadequately to conventional therapy. atopic dermatitisrinvoq is indicated for the treatment of moderate to severe atopic dermatitis in adults and adolescents 12 years and older who are candidates for systemic therapy. ulcerative colitisrinvoq is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis who have had an inadequate response, lost response or were intolerant to either conventional therapy or a biologic agent.  crohn’s diseaserinvoq is indicated for the treatment of adult patients with moderately to severely active crohn’s disease who have had an inadequate response, lost response or were intolerant to either conventional therapy or a biologic agent.

Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

amitriptylinehydrochloride 11,3 mg/stuk samenstelling overeenkomend met ; amitriptyline 10 mg/stuk - filmomhulde tablet - cellulose, gepoederd (e 460(ii)) ; croscarmellose natrium (e 468) ; ijzeroxide geel (e 172) ; ijzeroxide rood (e 172) ; lactose 1-water ; macrogol 3350 ; magnesiumstearaat (e 470b) ; maÏszetmeel ; polyvinylalcohol (e 1203) ; siliciumdioxide (e 551) ; talk (e 553 b) ; titaandioxide (e 171), ijzeroxide geel (e 172) ; ijzeroxide rood (e 172) ; lactose 1-water ; macrogol 3350 ; magnesiumstearaat (e 470b) ; maÏszetmeel ; polyvinylalcohol (e1203) ; povidon k 25 (e 1201) ; talk (e 553 b) ; titaandioxide (e 171)

Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

amitriptylinehydrochloride 56,6 mg/stuk samenstelling overeenkomend met ; amitriptyline 50 mg/stuk - filmomhulde tablet - cellulose, gepoederd (e 460(ii)) ; croscarmellose natrium (e 468) ; ijzeroxide geel (e 172) ; ijzeroxide rood (e 172) ; lactose 1-water ; macrogol 3350 ; magnesiumstearaat (e 470b) ; maÏszetmeel ; polyvinylalcohol (e 1203) ; siliciumdioxide (e 551) ; talk (e 553 b) ; titaandioxide (e 171), cellulose, gepoederd (e 460) ; croscarmellose natrium (e 468) ; ijzeroxide geel (e 172) ; ijzeroxide rood (e 172) ; lactose 1-water ; macrogol 3350 ; magnesiumstearaat (e 470b) ; maÏszetmeel ; polyvinylalcohol (e1203) ; siliciumdioxide (e 551) ; talk (e 553 b) ; titaandioxide (e 171), ijzeroxide geel (e 172) ; ijzeroxide rood (e 172) ; lactose 1-water ; macrogol 3350 ; magnesiumstearaat (e 470b) ; maÏszetmeel ; polyvinylalcohol, gedeeltelijk gehydrolyseerd (e1203) ; povidon k 25 (e 1201) ; talk (e 553 b) ; titaandioxide (e 171)

Europese Unie - Nederlands - EMA (European Medicines Agency)

omrix biopharmaceuticals n. v. - menselijk fibrinogeen, menselijk trombine - hemostase, chirurgisch - antihemorragica - evicel wordt gebruikt als ondersteunende behandeling bij operaties waarbij standaardchirurgische technieken onvoldoende zijn, ter verbetering van de hemostase. evicel is ook geïndiceerd als hechtdraad ondersteuning voor hemostase in vasculaire chirurgie.

Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

alfasan nederland b.v. - sulfasalazine - tablet - sulfasalazine 500 mg/stuk, - sulfasalazine - honden

Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

glaxosmithkline b.v. - a-california-7-2009 (h1n1)pdm09 achtige stam, gebruikt nib-74xp afgeleid van a-christchurch-16-2010 ; a-switzerland-9715293-2013 (h3n2)-achtige stam (a-switzerland-9715293-2013, nib-88) ; b-phuket-3073-2013-achtige stam (b-phuket-3073-2013, wild type) - suspensie voor injectie - dinatriumwaterstoffosfaat 12-water (e 339) ; kaliumchloride ; kaliumdiwaterstoffosfaat 0-water (e 340) ; magnesiumchloride 6-water (e 511) ; natriumchloride ; octoxinol ; polysorbaat 80 (e 433) ; tocoferol, d-alpha waterstofsuccinaat ; water voor injectie, - influenza, purified antigen

Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

bayer b.v. - acarbose; - tablet - acarbose

Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

medcor pharmaceuticals b.v. - acarbose; - tablet - acarbose

Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

bayer b.v. energieweg 1 3641 rt mijdrecht - acarbose - tablet - cellulose, microkristallijn (e 460) ; magnesiumstearaat (e 470b) ; maÏszetmeel ; siliciumdioxide (e 551), - acarbose