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Feldene (PIROXICAM)

Pfizer · FDA-approved approved Small molecule Verified Quality 70/100

Feldene works by blocking the production of prostaglandins, hormone-like substances that cause pain and inflammation.

Feldene (Piroxicam) is a nonsteroidal anti-inflammatory drug (NSAID) developed by Pfizer, targeting prostaglandin G/H synthase 1. It is a small molecule modality, approved by the FDA in 1982 for the treatment of osteoarthritis and rheumatoid arthritis. Feldene is now off-patent, with 18 generic manufacturers available. As a result, its commercial status is generic, and it is widely used to manage pain and inflammation. Key safety considerations include gastrointestinal side effects and potential interactions with other medications.

At a glance

Generic namePIROXICAM
SponsorPfizer
Drug classNonsteroidal Anti-inflammatory Drug [EPC]
TargetProstaglandin G/H synthase 1
ModalitySmall molecule
Therapeutic areaImmunology
PhaseFDA-approved
First approval1982

Mechanism of action

Piroxicam has analgesic, anti-inflammatory, and antipyretic properties.The mechanism of action of piroxicam, like that of other NSAIDs, is not completely understood but involves inhibition of cyclooxygenase (COX-1 and COX-2).Piroxicam is potent inhibitor of prostaglandin (PG) synthesis in vitro. Piroxicam concentrations reached during therapy have produced in vivo effects. Prostaglandins sensitize afferent nerves and potentiate the action of bradykinin in inducing pain in animal models. Prostaglandins are mediators of inflammation. Because piroxicam is an inhibitor of prostaglandin synthesis, its mode of action may be due to decrease of prostaglandins in peripheral tissues.

Approved indications

Boxed warnings

Common side effects

Drug interactions

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results

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