Fentanyl (Duragesic) Patch Recall, Possible Overdose & Death

In 2005, a number of deaths stemming from the use of the Duragesic Patch, also known as the Fentanyl Patch, prompted the Federal Drug Administration to issue a public health advisory regarding the risks involved with the drug. Starting in February 2008, various brands of patches have been recalled because of a product defect that can allow the fentanyl gel to leak out of the patch.

The defect is a slice, or a small cut, in the pouch that contains the medicine within the patch. This leads to direct absorption of the fentanyl gel through the skin, which can cause respiratory distress, and in some cases, death. Additionally, those applying the patches to patients can come into contact with the drug should the patch be faulty.

The dermal patches are prescribed for patients suffering from severe or chronic pain that is expected to last for more than a few weeks. Generally, those who use the patches have developed a tolerance for other painkillers, although some doctors have been known to prescribe the patch for patients with headaches and pain related to surgeries.

The drug contained inside the patches is a strong opioid - an extremely powerful medication - that is estimated to be 80 to 100 times stronger than morphine. Fentanyl is considered a Class II substance by the Drug Enforcement Administration, meaning it is associated with a high potential for abuse and a risk for fatal overdose.

The first recall is for 25- mcg Duragesic Patches from PriCara, with an expiration date that falls on or before December 2009. The generic equivalent of this patch, sold by Sandoz, is included in the recall. The patches are made by ALZA Corporation, which is a unit of Johnson & Johnson. The 25-mcg patches are generally prescribed for lower-weight patients, children and those who have recently started the prescription.

The second recall affects more than a dozen lots of patches of all strengths under the Actavis name. The patches are produced by Abrika Pharmaceuticals and can be identified by either name.

If you or a loved one are using Duragesic Patches and have experienced symptoms such as sleepiness, dizziness, trouble breathing or fainting, you can contact an attorney at FREIDIN · DOBRINSKY by calling 1-866-495-8060. Our consumer fraud attorneys will answer your questions free of charge, and we are here to help. We are investigating various Duragesic Patch complaints as part of a pending class action lawsuit. We have the experience in helping victims of Dangerous Products and Medical Malpractice cases and have capabilities to pursue justice for those who have been affected by this drug.