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Pronunciation | /paɪˈrɒksɪˌkæm/ |
Trade names | Feldene, others[1] |
Other names | Piroksikam, piroxikam |
AHFS/Drugs.com | Monograph |
MedlinePlus | a684045 |
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Routes of administration | By mouth |
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Pharmacokinetic data | |
Protein binding | 99%[4] |
Metabolism | Liver-mediated hydroxylation and glucuronidation[4] |
Elimination half-life | 50 hours[4] |
Excretion | Urine, faeces |
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ECHA InfoCard | 100.048.144 |
Chemical and physical data | |
Formula | C15H13N3O4S |
Molar mass | 331.35 g·mol−1 |
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Piroxicam is a nonsteroidal anti-inflammatory drug (NSAID) of the oxicam class used to relieve the symptoms of painful inflammatory conditions like arthritis.[4][5] Piroxicam works by preventing the production of endogenous prostaglandins which are involved in the mediation of pain, stiffness, tenderness and swelling.[4] The medicine is available as capsules, tablets and, in some countries, as a prescription-free gel 0.5%.[6] It is also available in a betadex formulation, which allows a more rapid absorption of piroxicam from the digestive tract.[4] Piroxicam is one of the few NSAIDs that can be given parenteral routes.[citation needed]
It was patented in 1968 by Pfizer and approved for medical use in 1979.[7] It became generic in 1992,[8] and is marketed worldwide under many brandnames.[1]
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