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Ketoprofen and Omeprazole

Luis Fernando Simoneti · FDA-approved active Small molecule

Ketoprofen inhibits prostaglandin synthesis via COX inhibition to reduce inflammation and pain, while omeprazole suppresses gastric acid production to protect against NSAID-induced ulcers.

Ketoprofen inhibits prostaglandin synthesis via COX inhibition to reduce inflammation and pain, while omeprazole suppresses gastric acid production to protect against NSAID-induced ulcers. Used for Rheumatoid arthritis with gastric protection, Osteoarthritis with gastric protection, Chronic pain conditions requiring NSAID therapy with reduced GI risk.

At a glance

Generic nameKetoprofen and Omeprazole
Also known asLower third molar surgery with Ketoprofen and Omeprazole
SponsorLuis Fernando Simoneti
Drug classNSAID + Proton pump inhibitor combination
TargetCOX-1/COX-2 (ketoprofen); H+/K+-ATPase (omeprazole)
ModalitySmall molecule
Therapeutic areaRheumatology / Pain Management / Gastroenterology
PhaseFDA-approved

Mechanism of action

This is a fixed-dose combination pairing an NSAID (ketoprofen) with a proton pump inhibitor (omeprazole). Ketoprofen blocks cyclooxygenase enzymes to reduce prostaglandin-mediated inflammation, pain, and fever. Omeprazole reduces gastric acid secretion by inhibiting the H+/K+-ATPase pump, thereby mitigating the gastrointestinal toxicity risk inherent to chronic NSAID use.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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