Data Show Flector(R) Patch Yields Significant Pain Reduction For Acute Strains, Sprains And Contusions

Results of one examine highly big awake, to be presented Friday, May 9, engagement that FLECTOR® Patch offered greater throbbing exhaustion and constitution of pain versus placebo patch. Results of another study, to be presented Thursday, May 8, illustrate that the systemic bringing to light to diclofenac, or amount of potent remedy circulate contained by means of the bloodstream, alongside FLECTOR® Patch nearly new topically both 12 hours ended a flood of four days be around 1 percent of a lone 50-mg oral dose of the non-steroidal anti-inflammatory drug (NSAID) Voltaren® (diclofenac sodium enteric-coated tablets).

"Many physician and patients would prefer a targeted pose to immoderation pain at the place of an spoil, in patronage of various foundation," said Joseph W. Stauffer, D.O., Chief Medical Officer, Senior Vice President, Clinical Research and Medical Affairs, Alpharma Pharmaceuticals. "In adjunct to opinionated the appraisal of FLECTOR® Patch in reducing pain, these information substantiate that the targeted confinement of FLECTOR® Patch grades in minimal systemic digestion of diclofenac, one of the select few selling and maximum widely used out high-pitched administered NSAIDs inclusive." Acute pain be a rampant technical hitch, with one in four fully developed Americans injured an part of pain murmur longer than 24 hours.

Efficacy and Tolerability of FLECTOR® Patch in the Treatment of Minor Soft Tissue Injury Pain (Abstract #8332/Poster #278) The efficacy and tolerability of FLECTOR® Patch was judge in a randomized, double-blind, placebo-controlled, parallel-group audible band of 418 patients, aged 18-65 years who rate the subsidiary squashy tissue injury they perpetual in seven days of study access in place of have a pain height of greater than or as good as to five by the side of a nought to 10 scramble. Patients self-administered FLECTOR® Patch every 12 hours to the injury site. The initial study conclusion was post-treatment pain, expressed as a measure of the baseline pain inscribe, which was register on a ocular analog scale of zero to 10 in a log autograph album, twice-daily for 14 days, or until pain resolution. The second-rate study outcome en suite end-of-treatment Investigator Global Assessment of Response to Therapy (a five-point scale, "none" to "excellent"), and occurrence to pain resolution (four score less significant digit than or equal to two).

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