Literature DB >> 1347468

Clinical tolerance to three 5-aminosalicylic acid releasing preparations in patients with inflammatory bowel disease intolerant or allergic to sulphasalazine.

M H Giaffer1, C J O'Brien, C D Holdsworth.   

Abstract

The clinical tolerance to three 5-aminosalicylic acid (5-ASA) releasing preparations (mesalazine, olsalazine and balsalazide) was assessed in a consecutive series of 43 patients with inflammatory bowel disease who were intolerant to sulphasalazine. The relative contributions to the side-effects of sulphasalazine made by its two components, 5-ASA and sulphapyridine, were also assessed in these patients. Thirty-nine (91%) patients were able to tolerate at least one of the three 5-ASA preparations. Only four (9%) patients were intolerant to all preparations, having adverse reactions previously experienced with sulphasalazine and presumably related to 5-ASA rather than sulphapyridine. The clinical tolerance to mesalazine (63%), olsalazine (70%) and balsalazide (70%) was similar, and tolerance to one drug only was found in nine (18%) patients. The commonest adverse reactions associated with 5-ASA preparations were gastrointestinal. Diarrhoea was a problem in five patients during treatment with olsalazine and three each while on mesalazine and balsalazide. Allergic reactions from 5-ASA preparations were uncommon; of ten patients with rash following sulphasalazine only one developed a rash with mesalazine. The results of this study indicate that the vast majority of patients with inflammatory bowel disease can be managed with at least one of these four 5-ASA containing preparations and that the side-effects of sulphasalazine are multifactorial in aetiology, some being due to the parent molecule, and some to one of its two metabolites, 5-ASA and sulphapyridine.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1347468     DOI: 10.1111/j.1365-2036.1992.tb00544.x

Source DB:  PubMed          Journal:  Aliment Pharmacol Ther        ISSN: 0269-2813            Impact factor:   8.171


  12 in total

1.  Mesalamine induced symptom exacerbation of ulcerative colitis: Case report and brief discussion.

Authors:  Maneesh Kumar Gupta; Scott Pollack; John J Hutchings
Journal:  World J Gastrointest Pharmacol Ther       Date:  2010-12-06

2.  New salicylates as maintenance treatment in ulcerative colitis.

Authors:  G Järnerot
Journal:  Gut       Date:  1994-09       Impact factor: 23.059

Review 3.  Oral 5-aminosalicylic acid for maintenance of remission in ulcerative colitis.

Authors:  Yongjun Wang; Claire E Parker; Brian G Feagan; John K MacDonald
Journal:  Cochrane Database Syst Rev       Date:  2016-05-09

Review 4.  Comparative tolerability of treatments for inflammatory bowel disease.

Authors:  R B Stein; S B Hanauer
Journal:  Drug Saf       Date:  2000-11       Impact factor: 5.606

Review 5.  How important is onset of action in ulcerative colitis therapy?

Authors:  Steven Masson; David Nylander; John C Mansfield
Journal:  Drugs       Date:  2005       Impact factor: 9.546

6.  Sulphasalazine and mesalazine: serious adverse reactions re-evaluated on the basis of suspected adverse reaction reports to the Committee on Safety of Medicines.

Authors:  R A J Ransford; M J S Langman
Journal:  Gut       Date:  2002-10       Impact factor: 23.059

Review 7.  Balsalazide: a review of its therapeutic use in mild-to-moderate ulcerative colitis.

Authors:  Richard B R Muijsers; Karen L Goa
Journal:  Drugs       Date:  2002       Impact factor: 9.546

8.  Mesalazine induced exacerbation of ulcerative colitis.

Authors:  K C Kapur; G T Williams; M C Allison
Journal:  Gut       Date:  1995-12       Impact factor: 23.059

Review 9.  Balsalazide.

Authors:  A Prakash; C M Spencer
Journal:  Drugs       Date:  1998-07       Impact factor: 9.546

Review 10.  Oral delayed-release mesalazine: a review of its use in ulcerative colitis and Crohn's disease.

Authors:  A Prakash; A Markham
Journal:  Drugs       Date:  1999-03       Impact factor: 11.431

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.