Reinstitution of gold therapy in rheumatoid arthritis after mucocutaneous reactions
- PMID: 127042
Reinstitution of gold therapy in rheumatoid arthritis after mucocutaneous reactions
Abstract
Gold therapy was successfully reinstituted in 28 of 30 patients with rheumatoid arthritis who had previously developed toxic, mucocutaneous reactions. At least six weeks after the reactions had completely cleared, patients were given 1 to 10 mg of gold sodium thiomalate (Myochrysine). This dose was increased every two to four weeks. An initial dose of 1 or 2 mg, with an interval of at least three weeks between injections, increasing not more than5 mg at each injection, is recommended.