Cyclosporin in rheumatoid arthritis - Monitoring for adverse effects and clinically significant drug interactions

Citation
B. Dijkmans et A. Gerards, Cyclosporin in rheumatoid arthritis - Monitoring for adverse effects and clinically significant drug interactions, BIODRUGS, 10(6), 1998, pp. 437-445
Citations number
45
Categorie Soggetti
Pharmacology
Journal title
BIODRUGS
ISSN journal
11738804 → ACNP
Volume
10
Issue
6
Year of publication
1998
Pages
437 - 445
Database
ISI
SICI code
1173-8804(199812)10:6<437:CIRA-M>2.0.ZU;2-K
Abstract
While cyclosporin has an established role in the treatment of rheumatoid ar thritis there is concern about adverse effects, mainly related to renal fun ction. With new interest being generated in cyclosporin combination therapy , and the availability of a new form of cyclosporin (cyclosporin microemuls ion), focus on adverse effects and drug interactions of this compound remai ns important. Over the years, rheumatologists have been aware of these adverse effects an d consensus meetings have resulted in guidelines for the use of cyclosporin , If these guidelines are followed, structural renal damage can be minimal, Cyclosporin should be started at a low dose and titrated against the highe st acceptable increase in serum creatinine, that is, a 30% increase over th e pretreatment value. At present, there is no evidence that cyclosporin in combination with other antirheumatics leads to increased toxicity, With reg ard to long term unwanted effects, neither the pattern nor the risk of mali gnancies associated with the use of cyclosporin seems to differ from other antirheumatics. The place of cyclosporin in the treatment of rheumatoid arthritis seems to be established. The most promising results will come from early rheumatoid arthritis combination studies involving cyclosporin with other antirheumati cs, especially methotrexate.