General information

Pyritinol (pyridoxine disulfide or pyrithioxine) is a sulfhydryl-containing compound, a dimer of 5-thiopyridoxine. It was used from 1961 onwards as a psychostimulant of doubtful efficacy, but apparently without adverse reactions, and then largely abandoned. When it was re-introduced in some countries for rheumatoid arthritis, adverse reactions were registered in 25% of patients.

Cross-allergy with d -penicillamine has been hypothesized to explain the apparently higher frequency of adverse reactions to pyritinol in patients with rheumatoid arthritis [ ].

In usual doses, 600–800 mg/day, pyritinol has a profile of adverse reactions reminiscent of that of penicillamine [ , ]. Some 40% of users have adverse reactions, leading to withdrawal in about 23% of the total. The most common are non-specific rashes and stomatitis; in addition, pemphigus, lichen planus, and photosensitivity have occurred. Gastrointestinal symptoms (diarrhea, gastralgia, nausea, loss of taste) can occur, but are less frequent than with penicillamine. Thrombocytopenia, reversible extramembranous glomerulonephritis with nephrotic syndrome [ ], a myasthenia-like picture, and acute polymyositis with positive rechallenge have also been described [ ].

In a collaborative study of the French Pharmacovigilance Centers there were 23 reports of suspected reactions to pyritinol, including four cases of pemphigus, three of agranulocytosis (but other drugs taken were oxyphenbutazone or clomipramine), two of nephrosis, and two of a lupus-like syndrome [ ].

Drug studies

Comparative studies

In a multicenter, double-blind study, patients with rheumatoid arthritis took pyritinol 600 mg/day or auranofin 6 mg/day for 1 year [ ]. Of 139 patients randomized to pyritinol, 61 (44%) dropped out because of adverse events or response failure compared with 44 (31%) of the 142 patients randomized to auranofin. Among the rest, adverse events occurred in 64% of patients taking pyritinol and in 58% of patients taking auranofin: the main events were mucocutaneous symptoms (pyritinol 36%, auranofin 23%) and gastrointestinal complaints (pyritinol 30%, auranofin 37%). There were single cases of proteinuria, hepatic abnormalities, and hematological abnormalities in both groups.

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