MESALAZINE - A GLOBAL SAFETY EVALUATION

The potential benefit of sulphasalazine in inflammatory bowel disease is limited by the wide variety of side effects that occur in about one-third of treated patients. Most of the side effects of sulphasalazine are due to the sulphapyridine moiety. Claversal has the advantage of delivering the active ingredient of sulphasalazine-mesalazine- without the undesirable effects of sulphapyridine. Four international multicentre trials involving 932 patients with ulcerative colitis or Crohn's disease compared 0.75 g/ day or 1.5 g/day mesalazine, 1.5 g/day or 3.0 g/day sulphasalazine, or placebo. Forty-seven (14% of 331 patients receiving mesalazine reported adverse events, whereas 33 (23% of 144 patients receiving sulphasalazine and 23 (19% of 123 patients receiving placebo reported adverse effects. When lower doses of both mesalazine (0.75 g/day) and sulphasalazine (1.5 to 2.0 g/day) were evaluated in a maintenance trial, the percentage of adverse events was similar for both drugs-14% and 12% respectively. In these trials the incidence of adverse effects was similar with both doses of mesalazine; however, doubling the sulphasalazine dose resulted in a twofold increase in adverse effects. In contrast, mesalazine appeared not to induce dose-related effects, suggesting that patients may be able to tolerate even higher mesalazine doses than those studied. The withdrawal rate owing to adverse events in all four controlled trials was similar for patients treated with mesalazine (6% and sulphasalazine (8% Results of an open postmarketing sampling trial of just over 1700 patients in Germany showed a low overall incidence of adverse effects (3% with mesalazine and none of the rare, more serious effects, such as hepatotoxicity, agranulocytosis, or pulmonary complications. Less than 1% of all patients discontinued the therapy as a result of adverse events. In addition, approximately 30,000 patients in Germany have taken mesalazine since its introduction. With the exception of three reports of pancreatitis (a rare but documented event with sulphasalazine), most adverse effects reported to date have been minor. Mesalazine has been shown to provide the therapeutic benefits of sulphasalazine with an improved safety profile. © 1990 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted.