FDA pulls Propoxyphene products off the Market

The FDA watches risk factors of different drugs and occasionally they will either put out a warning or in some cases pull a product all together. Well today one product type for pain relief did get pulled

On July 7, 2009, the Food and Drug Administration (FDA) announced actions it was taking to reduce the risk of overdose in people who use pain medications, such as Darvon and Darvocet. These medications contain the drug propoxyphene, which is linked to death from overdoses.

FDA finds there is evidence that propoxyphene can effectively treat pain at recommended doses. But because of the drug’s potential risks, the agency is requiring manufacturers to provide more information to help physicians and patients decide whether propoxyphene is the appropriate pain treatment.

About Propoxyphene

* Propoxyphene has been on the market since 1957.
* It is a widely prescribed medication in a group of drugs known as opioids, and is used to treat mild to moderate pain.
* The most frequent side effects of propoxyphene include lightheadedness, dizziness, sedation, nausea, and vomiting.

Advice for Consumers

* Be aware of all the risks associated with pain medication, including propoxyphene, when making decisions on how to treat pain. All pain medicines have side effects.
* Talk to your health care professional to decide on the appropriate pain treatment for you if you need relief from pain.

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