Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

abbvie a/s - clostridium botulinum, type a toxin - pulver til injektionsvæske, opløsning - 100 enheder

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

abbvie a/s - clostridium botulinum, type a toxin - pulver til injektionsvæske, opløsning - 200 enheder

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

abbvie a/s - carmellosenatrium - øjendråber, opløsning, enkeltdosisbeholder - 10 mg/ml

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

abbvie a/s - carbidopa, levodopa - enteralgel - 20+5 mg/ml

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

abbvie a/s - sevofluran - væske til inhalationsdamp

Den europeiske union - dansk - EMA (European Medicines Agency)

abbvie deutschland gmbh & co. kg - risankizumab - psoriasis; arthritis, psoriatic - immunosuppressiva - plaque psoriasisskyrizi is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. psoriatic arthritisskyrizi, alone or in combination with methotrexate (mtx), is indicated for the treatment of active psoriatic arthritis in adults who have had an inadequate response or who have been intolerant to one or more disease-modifying antirheumatic drugs (dmards). crohn's diseaseskyrizi is indicated for the treatment of adult patients with moderately to severely active crohn's disease who have had an inadequate response to, lost response to, or were intolerant to conventional therapy or a biologic therapy.

Den europeiske union - dansk - EMA (European Medicines Agency)

abbvie deutschland gmbh & co. kg - upadacitinib - arthritis, reumatoid - 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.

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

abbvie a/s - foscarbidopa, foslevodopa - infusionsvæske, opløsning - 240+12 mg/ml

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

idt biologika gmbh - clostridium botulinum type c, stamme stockholm, toxoid, mink parvovirus, stamme e-mink f1 (inaktiveret), pseudomonas aeruginosa habs serotype 5 (inaktiveret), pseudomonas aeruginosa habs serotype 6 (inaktiveret), pseudomonas aeruginosa habs serotype 7-8 (inaktiveret) - injektionsvæske, suspension - pelsdyr (f.eks. mink)

Den europeiske union - dansk - EMA (European Medicines Agency)

cp-pharma handelsgesellschaft mbh - dexmedetomidine hydrochloride - psycholeptics, hypnotika og sedativa - cats; dogs - ikke-invasiv, mild til moderat smertefuld, procedurer og undersøgelser, der kræver tilbageholdenhed, sedation og analgesi hos hunde og katte. dyb sedation og analgesi hos hunde i samtidig brug med butorphanol til medicinske og mindre kirurgiske indgreb. premedicinering hos hunde og katte før induktion og vedligeholdelse af generel anæstesi.