PMID- 12904092 OWN - NLM STAT- MEDLINE DCOM- 20031008 LR - 20191107 IS - 1474-0338 (Print) IS - 1474-0338 (Linking) VI - 2 IP - 4 DP - 2003 Jul TI - Safety and efficacy of disease-modifying antirheumatic agents in rheumatoid arthritis and juvenile rheumatoid arthritis. PG - 347-65 AB - The definition of disease-modifying antirheumatic drugs (DMARDs) has changed dramatically over the last decade. Current expectations of efficacy now include amelioration of signs and symptoms of disease activity as well as slowing, if not complete cessation, of disease progression as evidenced by Xray progression and significant improvement of patient function. Rheumatologists assess the safety profile of these agents more critically in an attempt to increase the risk:benefit profile. Traditional agents, such as methotrexate (MTX), sulfasalazine and leflunomide have provided patients with substantial relief of symptoms and some decrease of X-ray progression but have been hampered by the frequent occurrence of significant adverse events (AEs) and inability to maintain benefit for a prolonged period of time. With the increased understanding of the basic mechanism of the disease process, there has been the introduction of four biological disease-modifying agents introduced into clinical practice which have substantially increased the risk:benefit ratio for patients with various rheumatic diseases. FAU - Fleischmann, Roy AU - Fleischmann R AD - University of Texas Southwestern Medical Center at Dallas, St Paul University Hospital, 5939 Harry Hines Boulevard, Suite 400, Dallas, Texas 75235, USA. royfleischmann@radiantresearch.com LA - eng PT - Journal Article PT - Review PL - England TA - Expert Opin Drug Saf JT - Expert opinion on drug safety JID - 101163027 RN - 0 (Antirheumatic Agents) SB - IM MH - Antirheumatic Agents/*therapeutic use MH - Arthritis, Juvenile/drug therapy MH - Arthritis, Rheumatoid/*drug therapy MH - Clinical Trials as Topic MH - Disease Progression MH - Drug Therapy, Combination MH - Humans MH - Product Surveillance, Postmarketing MH - Risk Assessment RF - 205 EDAT- 2003/08/09 05:00 MHDA- 2003/10/09 05:00 CRDT- 2003/08/09 05:00 PHST- 2003/08/09 05:00 [pubmed] PHST- 2003/10/09 05:00 [medline] PHST- 2003/08/09 05:00 [entrez] AID - 10.1517/14740338.2.4.347 [doi] PST - ppublish SO - Expert Opin Drug Saf. 2003 Jul;2(4):347-65. doi: 10.1517/14740338.2.4.347.