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Back to FDA Approvals 2004

Combunox

Generic Name: oxycodone and ibuprofen tablets
Date of Approval: November 26, 2004
Company: Forest Laboratories, Inc.
Treatment for: Moderate to Severe Pain

The U.S. Food and Drug Administration (FDA) has approved Combunox (Oxycodone HCl and Ibuprofen) Tablets (CII), the first and only fixed-dose combination of the opioid oxycodone HCl (5 mg) and the nonsteroidal anti-inflammatory drug (NSAID) ibuprofen (400 mg), for the short-term management of acute, moderate to severe pain.

Forest expects to make Combunox available in the U.S. early next year.

About Combunox and Acute Pain
Combunox combines oxycodone, which is generally considered up to 1.5 times more potent than hydrocodone and nearly ten times more potent than codeine as a narcotic analgesic, with ibuprofen at its typical analgesic dose. The clinical benefit of Combunox is attributed to the distinct actions of each component.

The FDA approved Combunox based on a review of efficacy data from three double-blind, placebo-controlled trials. In these trials, Combunox provided significantly greater pain relief than oxycodone 5 mg alone, ibuprofen 400 mg alone, or placebo. Pooled data from the complete safety database, which included a multiple-dose study, found Combunox to be safe and well tolerated. The most common side effects included nausea, vomiting, somnolence, dizziness, and headache, which typically are present with all products containing opioids. Combunox is a Schedule II controlled substance.

Acute pain is generally caused by injury or surgery, and is the most common reason why patients seek medical attention (25 million Americans annually). In addition to unnecessary suffering, inadequately controlled acute pain causes complications that can increase the length of hospital stays, re-hospitalization rates, and outpatient visits.

For more information, please visit www.combunox.com.