-February 13, 2008
Patches that contain the painkiller fentanyl were recently recalled by the FDA.
The recall is reportedly due to new found risks that have been associated with the prescription painkiller.
About the Patches
The patches containing fentanyl have been sold in the United States under the name Duragesic by PriCara.
The recall includes 25-microgram-er-hour patches that have expiration dates on or before December 2009.
Risks of Medication
According to reports, some of the patches could have a cut in the lining where the drug is kept, which comes in a gel form.
If the fentanyl gel is leaked into the packaging, then the patient or caregiver could potentially become exposed to a great deal of the powerful drug.
As a result, both patients and caregivers are at risk of having an overdose if wrongfully exposed to a large amount of the medication.
Warning Issued by FDA
In December, the FDA reportedly issued a warning explaining the risks associated with the painkiller patch and detailing the dangers of misusing the drug.
Although the patch is usually prescribed to patients experiencing chronic pain from cancer or narcotics, the FDA discovered that many doctors were prescribing it to those with headaches and post-surgical pain.
(Source: Associated Press)
Have you or someone you know been harmed by using the Durgesic patch? If so, please contact us to speak with an experienced attorney who will enable you to receive the compensation you deserve.
