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Injured by the Duragesic Patch?

Keywords: Duragesic | Lawyer | Death | Attorney | Injury | Overdose | Lawsuit

On July 15, 2005 the FDA issued a Public Health Advisory concerning the use of Duragesic Patches (Fentanyl transdermal) in response to reports of deaths in patients using the patch. The FDA is conducting an investigation into the deaths associated with these patches.

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The Agency has been examining the circumstances of product use to determine if the reported adverse events may be related to inappropriate use of the patch or factors related to the quality of the product. It is possible that some patients and their health care providers may not be completely aware of the dangers of these potent narcotic drug products and the important recommendations regarding their safe use.

There has been an expanded recall of Duragesic Patches due to possible leaks. Janssen Pharmaceutica, the manufacturer of the Duragesic Patch notified healthcare professionals of an expanded recall of the Duragesic 75 mcg/h, in February 2004. Four additional lots have been subject to the present expanded recall. Some patches from the recalled lots may leak medication due to improper sealing of one of their edges.

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If the medication leaks out of the patch, exposure to the medication can result in inadvertent ingestion or increased transdermal absorption of the active opiate component fentanyl, leading to potentially life-threatening complications. In addition, leakage of the medication could lead to inadequate dosing, resulting in treatment failure and/or opiate withdrawal.

The Duragesic Patch is indicated for the management of severe, chronic pain (such as cancer pain) that cannot be managed with less powerful drugs such as acetaminophen-opioid combinations and nonsteroidal analgesics.

Moreover, only patients who are already on and tolerant to opioid therapy, and require continuous opioid administration should use the patch. Approved by the U.S. Food and Drug Administration (FDA) in 1990, the Duragesic patch releases fentanyl, a strong opioid, through the skin at a fixed rate for 72 hours. The patch is available only by prescription.

If you or a loved one used a Duragesic Patch and suffered side effects, please fill out the form at the right for a free case evaluation by a qualified drug side effects lawyer / attorney.
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Watson Recalls Fentanyl Pain Patches Over Leakage Worries

Aug 12, 2008 | Parker Waichman Alonso LLP
Fentanyl pain patches are being recalled by Watson Pharmaceuticals because some of them may leak fentanyl gel.  Exposure to fentanyl gel may lead to serious adverse events, including respiratory depression and possible overdose, which may be fatal. Fentanyl is a highly addictive opiate that is 80 times more potent 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...

Actavis Recalls More Fentanyl Pain Patches

Mar 3, 2008 | Parker Waichman Alonso LLP
More Fentanyl Pain Patches have been recalled by Actavis Inc due to a possible defect that could cause fentanyl to leak from the Actavis pain patches.  Actavis had recalled 14 lots of the Fentanyl Pain Patches in  mid-February.  Actavis said the remaining lots of the fentanyl transdermal system patches are being recalled as a precautionary measure because the company lacks insurance that all patches are free from defectsFentanyl transdermal patches are indicated for the...

Another Fentanyl Pain Patch Recall

Feb 18, 2008 | Parker Waichman Alonso LLP
Another fentanyl pain patch has been recalled today, amid concerns that such pain patches put users at risk of accidental fentanyl overdose.  Today’s fentanyl pain patch recall was issued by Activis Inc., which is recalling 14 lots of its Fentanyl transdermal system CII patches sold in the United States by its subsidiary Actavis South Atlantic LLC  from wholesalers and pharmacies as a precaution.  The recalled patches were manufactured by Corium International Inc., a...

Duregesic Patch Recall Adds to Johnson & Johnson Patch Woes

Feb 13, 2008 | Parker Waichman Alonso LLP
The Duragesic Pain Patch has been recalled by Johnson & Johnson because defects in the manufacture of the patch could lead to accidental overdoses. Johnson & Johnson is recalling about 32 million of the fentanyl-containing Duragesic Pain Patches, and the company estimates that about two out of every million patches could be defective. The Duragesic and other similar pain patches are meant to treat persistent, moderate to severe chronic pain in opioid-tolerant patients 2 years of age or...

Duragesic Pain Patch, Other Fentanyl Pain Patches Still Killing People, FDA Warns

Dec 21, 2007 | Parker Waichman Alonso LLP
The Duragesic patch and other generic fentanyl pain patches are still killing people, the Food & Drug Administration (FDA) warned today.  The Duragesic pain patch, marketed by Johnson & Johnson, and other generic pain patches, emit the powerful narcotic painkiller fentanyl.  These transdermal pain patches were approved to treat pain in people who use narcotics, such as cancer patients.  Today’s FDA notice is the second time since 2005 that the agency has warned of...

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