FDA ANNOUNCES DARVON RECALL: In November 2010, The US Food and Drug Administration announced a nationwide recall of this drug due to its use being linked to a high number of heart problems, as well as overdose and suicide.

DARVON (Darvocet) is reported to have caused serious injury to many thousands of users in the U.S. who have begun filing claims in the U.S. against Xanodyne Pharmaceutical seeking to recover financial compensation as a result of their suffering from heart attacks, strokes, heart rhythm abnormalities (arrhythmia) or other serious injuries and even deaths from the use of this drug.

This pain control medication, with properties similar to codeine, is an enormously popular drug used by millions in the treatment of mild to moderate pain. Also marketed as Darvocet, a compound containing both propoxyphene and acetaminophen, is one of the most popular pain relieving drugs in the U.S. The active medication–propoxyphene–relieves pain by acting on the central nervous system; however, its use has been linked over the years to thousands of deaths and serious injuries, most recently to potentially fatal heart rhythm abnormalities (arrhythmia).

DARVON (Darvocet) FDA BLACK BOX WARNING: The Food and Drug Administration has mandated that all DARVON (Darvocet) packages contain a black box label to warn consumers regarding the higher risks associated with consumption of these drugs.

Have you or a loved one suffered from any of the following serious side effects associated with Darvon

(Darvocet), such as:

• Heart Attack

• Stroke

• Heart Arrythmia

• Suicide

• Overdose

• Death

• Any other serious side effects

If the answer is yes, a lawyer with experience in the ongoing Darvon (Darvocet) litigation can help evaluate your claim at no charge. The Darvon recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by going to http://darvon-lawsuitattorney.com/.

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