Open AccessThe toxicity pattern of d‐penicillamine therapy
Author(s) -
Kean Walter F.,
Dwosh Isaac L.,
Anastassiades Tassos P.,
Ford Peter M.,
Kelly H. Garfield
Publication year - 1980
Publication title -
arthritis & rheumatism
Language(s) - English
Resource type - Journals
eISSN - 1529-0131
pISSN - 0004-3591
DOI - 10.1002/art.1780230205
Subject(s) - penicillamine , medicine , toxicity , proteinuria , rheumatoid arthritis , surgery , gastroenterology , kidney
One hundred and one patients with rheumatoid arthritis were followed prospectively to assess the efficacy and toxicity of therapy with D‐penicillamine. After a mean total followup of 11.5 months (38 patients have completed 2 years of followup) there was a 70% overall improvement rate with 2 complete remissions. Sixty‐one patients developed 84 separate toxic reactions, 36 of which required drug withdrawal. Skin rashes (27/84), proteinuria (15/84), low platelets (14/84), and taste abnormalities (10/84) were the most common side effects of therapy at a mean D‐penicillamine dose of 463 mg/ day. The majority of toxic reactions (85%) occurred in the first 6 months, but proteinuria and thrombocytopenia were more common in the 6 to 12 month treatment period. Previous gold toxicity was a risk factor for developing D‐penicillamine toxicity (10/13). Our observations suggest that D‐penicillamine related toxicity is a major problem even at 500 mg/day, but the drug can be used with an increased safety margin after 9 months of continuous therapy.