Propoxyphene was first approved by the U.S. Food and Drug Administration (FDA) in 1957 as a pain reliever, and has since been used by about 10 million patients. However, the drug was recently pulled off the market, according to MedScape.com.
Five years ago, the drug was banned in the United Kingdom because it posed a risk to patients of suicide. In 2009, it was taken off the market in Europe because of worries about overdoses. Any Kentucky Darvocet side effect attorney would want the public to know that Darvocet has now been taken off the market in the U.S. because of concern over arrhythmias.