Meloxicam in rheumatoid arthritis

Expert Opin Drug Metab Toxicol. 2005 Dec;1(4):739-51. doi: 10.1517/17425255.1.4.739.


Rheumatoid arthritis (RA), a chronic inflammatory multisystem disorder marked by joint pain, stiffness, swelling and multiple systemic involvements, requires a multifaceted approach for its management. It includes symptomatic treatment with analgesics as well as disease-modifying medications to alter the course of RA over time. NSAIDS have been widely used for their symptomatic effects, but their use is not free from adverse effects, which may include life-threatening adverse events such as gastrointestinal (GI) bleeding and perforation. Meloxicam, an oxicam derivative that is a member of the enolic acid group of NSAIDs, has recently been approved by the US FDA for use in RA and osteoarthritis. At the FDA-recommended doses meloxicam is COX-2 preferential. By virtue of this COX-2 preferential activity it is expected to have lower GI toxicity as compared with COX-2 nonselective NSAIDs. Clinical trials have shown that meloxicam at 7.5 - 15 mg/day is as effective as diclofenac, piroxicam and naproxen as an anti-inflammatory and analgesic, and was associated with fewer GI adverse effects.

Publication types

  • Review

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use*
  • Arthritis, Rheumatoid / drug therapy*
  • Cardiovascular System / drug effects
  • Cyclooxygenase Inhibitors / therapeutic use*
  • Gastrointestinal Tract / drug effects
  • Humans
  • Kidney / drug effects
  • Meloxicam
  • Thiazines / adverse effects
  • Thiazines / pharmacokinetics
  • Thiazines / pharmacology
  • Thiazines / therapeutic use*
  • Thiazoles / adverse effects
  • Thiazoles / pharmacokinetics
  • Thiazoles / pharmacology
  • Thiazoles / therapeutic use*


  • Anti-Inflammatory Agents, Non-Steroidal
  • Cyclooxygenase Inhibitors
  • Thiazines
  • Thiazoles
  • Meloxicam