Malta - inglese - Medicines Authority

central procurement & supplies unit ub002 industrial estate, san gwann sgn 3000, malta - sodium aurothiomalate - solution for injection - sodium aurothiomalate 50 mg - antiinflammatory and antirheumatic products

Irlanda - inglese - HPRA (Health Products Regulatory Authority)

may & baker limited - withdrawn form - 1 milligram

Irlanda - inglese - HPRA (Health Products Regulatory Authority)

may & baker limited - withdrawn form - 5 milligram

Australia - inglese - Department of Health (Therapeutic Goods Administration)

amdipharm mercury australia pty ltd - auranofin, quantity: 3 mg - tablet, film coated - excipient ingredients: titanium dioxide; maize starch; lactose monohydrate; magnesium stearate; iron oxide yellow; microcrystalline cellulose; hypromellose; purified water; sodium starch glycollate; propylene glycol; ethanol - indications as at 14 november 2000: adjunctive treatment of active classical or definite rheumatoid arthritis in adults who have an insufficient therapeutic response to, or are intolerant of, an adequate trial of a baseline therapeutic program, including among other measures, full doses of one or more non-steroidal anti-inflammatory drugs. ridaura is not indicated in non-rheumatoid arthropathies such as osteoarthrosis. ridaura should be added to a comprehensive baseline therapeutic program.

Australia - inglese - Department of Health (Therapeutic Goods Administration)

auranofin -