New Zealand - English - Medsafe (Medicines Safety Authority)

douglas pharmaceuticals limited - urokinase 500000 [iu] (ex italy) - powder for injection - 500000 iu - active: urokinase 500000 [iu] (ex italy) excipient: aprotinin mannitol sodium chloride water for injection

New Zealand - English - Medsafe (Medicines Safety Authority)

douglas pharmaceuticals limited - urokinase 5000 [iu] (ex italy) - powder for injection - 5000 iu - active: urokinase 5000 [iu] (ex italy) excipient: aprotinin dibasic sodium phosphate disodium edetate dihydrate mannitol sodium chloride water for injection

Ireland - English - HPRA (Health Products Regulatory Authority)

leo laboratories limited - 5,000 international unit

Ireland - English - HPRA (Health Products Regulatory Authority)

leo laboratories limited - 25,000 milligram

Ireland - English - HPRA (Health Products Regulatory Authority)

leo laboratories limited - 100,000 international unit

Egypt - English - EDA (Egyptian Drug Authority)

welding-medac - vial

Bangladesh - English - DGDA (Directorate General of Drug Administration)

beacon pharmaceuticals plc - urokinase - injection - 500000 iu/10 ml

European Union - English - EMA (European Medicines Agency)

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).

Ireland - English - HPRA (Health Products Regulatory Authority)

sanofi-synthelabo ireland ltd - urokinase -

India - English - Central Drugs Standard Control Organization

dabur ph. - urokinase - vial - 250000 i.u. - vial