Piroxicam is a nonsteroidal anti-inflammatory drug (NSAID) used in the treatment of osteoarthritis, rheumatoid arthritis, and ankylosing spondylitis to relieve pain and inflammation. Piroxicam is primarily metabolized by CYP2C9.
Piroxicam (Dosage)
Piroxicam is primarily metabolized by CYP2C9. People with reduced CYP2C9 activity have a higher exposure to piroxicam and a higher risk of side effects.
MECHANISM OF ACTION
Piroxicam is an inhibitor of cyclooxygenase enzymes that acts by reducing the synthesis of prostaglandins, substances that mediate pain, inflammation and fever. Piroxicam also inhibits the migration of leukocytes to the inflammatory focus and inhibits platelet aggregation.
CONTRAINDICATIONS
Treatment with piroxicam is contraindicated in patients with hypersensitivity to piroxicam or to any of the components of the medicine, if they have had reactions to acetylsalicylic acid or another NSAID, a history of asthma, urticaria or other allergic-type reactions after taking acetylsalicylic acid or another NSAID, and after coronary artery bypass graft (CABG) surgery. In patients with gastric ulcers, a history of gastrointestinal bleeding or perforation, patients with inflammatory bowel disease, patients with severe heart or liver failure, and in patients who are taking anticoagulants. Piroxicam should also be avoided in pregnant women from the third trimester onwards and during lactation.
SIDE EFFECTS
The most frequent side effects are mild headache, dizziness, drowsiness, nausea, abdominal pain, dyspepsia, diarrhea, vomiting, alterations in blood cell count, loss of appetite, increased blood sugar levels, and swelling of the ankles.
Like all NSAIDs, piroxicam increases the risk of serious cardiovascular problems (myocardial infarction and stroke), as well as severe gastrointestinal disorders such as bleeding, ulceration and perforation.
INTERACTIONS
Piroxicam may interact with corticosteroids, anticoagulants, antiplatelet agents, lithium, selective serotonin reuptake inhibitor antidepressants (SSRIs), immunosuppressants (cyclosporine and tacrolimus), sulfonylureas, methotrexate at doses equal to or greater than 15mg/week (at low doses if there is combined treatment, blood values and kidney function should be closely monitored).
BRAND NAMES
- Feldene®
Genes analyzed
Bibliography
Dean L. Piroxicam Therapy and CYP2C9 Genotype. 2019 Feb 11. In: Pratt VM, Scott SA, Pirmohamed M, Esquivel B, Kattman BL, Malheiro AJ, editors. Medical Genetics Summaries [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 2012–.
Perini JA, Vianna-Jorge R, Brogliato AR, Suarez-Kurtz G. Influence of CYP2C9 genotypes on the pharmacokinetics and pharmacodynamics of piroxicam. Clin Pharmacol Ther. 2005 Oct;78(4):362-9.
Theken KN, Lee CR, Gong L, et al. Clinical Pharmacogenetics Implementation Consortium Guideline (CPIC) for CYP2C9 and Nonsteroidal Anti-Inflammatory Drugs. Clin Pharmacol Ther. 2020 Aug;108(2):191-200.
