alprolix 250unit powder and solvent for solution for injection vials
swedish orphan biovitrum ltd - eftrenonacog alfa - powder and solvent for solution for injection - 250unit
alprolix 500unit powder and solvent for solution for injection vials
swedish orphan biovitrum ltd - eftrenonacog alfa - powder and solvent for solution for injection - 500unit
alprolix 1,000unit powder and solvent for solution for injection vials
swedish orphan biovitrum ltd - eftrenonacog alfa - powder and solvent for solution for injection - 1000unit
alprolix 2,000unit powder and solvent for solution for injection vials
swedish orphan biovitrum ltd - eftrenonacog alfa - powder and solvent for solution for injection - 2000unit
alprolix 3,000unit powder and solvent for solution for injection vials
swedish orphan biovitrum ltd - eftrenonacog alfa - powder and solvent for solution for injection - 3000unit
xiapex 0.9mg powder and solvent for solution for injection vials
swedish orphan biovitrum ltd - collagenase clostridium histolyticum - powder and solvent for solution for injection - 900microgram
kineret 100mg0.67ml solution for injection pre-filled syringes
swedish orphan biovitrum ltd - anakinra - solution for injection - 150mg/1ml
alprolix
swedish orphan biovitrum ab (publ) - eftrenonacog alfa - hemophilia b - vitamin k and other hemostatics, blood coagulation factors - treatment and prophylaxis of bleeding in patients with haemophilia b (congenital factor ix deficiency).
kineret
swedish orphan biovitrum ab (publ) - anakinra - arthritis, rheumatoid; covid-19 virus infection - immunosuppressants - rheumatoid arthritis (ra)kineret is indicated in adults for the treatment of the signs and symptoms of ra in combination with methotrexate, with an inadequate response to methotrexate alone.covid-19kineret is indicated for the treatment of coronavirus disease 2019 (covid-19) in adult patients with pneumonia requiring supplemental oxygen (low- or high-flow oxygen) who are at risk of progressing to severe respiratory failure determined by plasma concentration of soluble urokinase plasminogen activator receptor (supar) ≥ 6 ng/ml.periodic fever syndromeskineret is indicated for the treatment of the following autoinflammatory periodic fever syndromes in adults, adolescents, children and infants aged 8 months and older with a body weight of 10 kg or above:cryopyrin-associated periodic syndromes (caps)kineret is indicated for the treatment of caps, including:neonatal-onset multisystem inflammatory disease (nomid) / chronic infantile neurological, cutaneous, articular syndrome (cinca)muckle-wells syndrome (mws)familial cold autoinflammatory syndrome (fcas)familial mediterranean fever (fmf)kineret is indicated for the treatment of familial mediterranean fever (fmf). kineret should be given in combination with colchicine, if appropriate.still’s diseasekineret is indicated in adults, adolescents, children and infants aged 8 months and older with a body weight of 10 kg or above for the treatment of still’s disease, including systemic juvenile idiopathic arthritis (sjia) and adult-onset still’s disease (aosd), with active systemic features of moderate to high disease activity, or in patients with continued disease activity after treatment with non-steroidal anti-inflammatory drugs (nsaids) or glucocorticoids.kineret can be given as monotherapy or in combination with other anti-inflammatory drugs and disease-modifying antirheumatic drugs (dmards).
empaveli pegcetacoplan 1080 mg/20 ml injection solution vial
swedish orphan biovitrum pty ltd - pegcetacoplan, quantity: 1080 mg - injection, solution - excipient ingredients: water for injections; sodium hydroxide; sodium acetate trihydrate; glacial acetic acid; sorbitol - empaveli is indicated in the treatment of adult patients with paroxysmal nocturnal haemoglobinuria (pnh) who have an inadequate response to, or are intolerant of, a c5 inhibitor.