Ventizolve 1,26 mg/dosis næsespray, opløsning i enkeltdosisbeholder Данска - Дански - Lægemiddelstyrelsen (Danish Medicines Agency)

ventizolve 1,26 mg/dosis næsespray, opløsning i enkeltdosisbeholder

dne pharma as - naloxonhydrochlorid (vandfrit) - næsespray, opløsning i enkeltdosisbeholder - 1,26 mg/dosis

Rinvoq Европска Унија - Дански - EMA (European Medicines Agency)

rinvoq

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.

Lumeblue (previously known as Methylthioninium chloride Cosmo) Европска Унија - Дански - EMA (European Medicines Agency)

lumeblue (previously known as methylthioninium chloride cosmo)

alfasigma s.p.a. - methylthioniniumchlorid - colorectal neoplasms; colonoscopy - other diagnostic agents - lumeblue is indicated as a diagnostic agent enhancing visualisation of colorectal lesions in adult patients undergoing screening or surveillance colonoscopy.

Porcilis Ery+Parvo+Lepto injektionsvæske, suspension Данска - Дански - Lægemiddelstyrelsen (Danish Medicines Agency)

porcilis ery+parvo+lepto injektionsvæske, suspension

pharmaménta aps - erysipelothrix rhusiopathiae serotype 2, stamme m2 (inaktiveret), leptospira interrogans serogruppe australis serovar bratislava (stamme as-05-073), leptospira interrogans serogruppe canicola serovar portland-vere (stamme ca-12-000), leptospira interrogans serogruppe grippotyphosa serovar dadas (stamme gr-01-005), leptospira interrogans serogruppe icterohaemorragiae serovar copenhageni (stamme ic-02-001), leptospira interrogans serogruppe pomona, stamme po-01-000 (inaktiveret), leptospira santarosai serogruppe tarassovi serovar gatuni (strain s1148/02), porcin parvovirus, stamme 014 (inaktiveret) - injektionsvæske, suspension

Adrovance Европска Унија - Дански - EMA (European Medicines Agency)

adrovance

n.v. organon - colecalciferol, alendronic acid (as sodium trihydrate) - osteoporose, postmenopausale - narkotika til behandling af knoglesygdomme - behandling af postmenopausal osteoporose hos patienter med risiko for vitamin d-insufficiens. adrovance reducerer risikoen for vertebrale og hoftebrud.