Fentanyl is a medication that is prescribed to those with intense pain due to chronic or fatal illnesses. The composition of Fentanyl is similar to morphine and heroin, as it contains a synthetic opiate.

An overdose of Fentanyl will cause symptoms of respiratory depression and eventually respiratory arrest.

In February, the U.S. Food and Drug Association (FDA) issued it’s second warning regarding the misuse of Fentanyl since 2005.

Both patient and doctor error have lead to numerous fatalities through the misuse of Fentanyl. The FDA has only approved the use of Fentanyl for those with chronic pain, who are already accustomed to the use of opioids.

In order for the patient to be accustomed to an opioid, they must have consistently used the medication 24-hours a day for a week or more.

The FDA has been alerted to physicians prescribing Fentanyl to patients with non-chronic pain. Doctors have prescribed Fentanyl to patients suffering from post-surgery pain, migraine headaches and those that have never taken an opioid medication.

Accidental overdoses of Fentanyl have also been linked to frequent application of the pain patches. Another common misuse is from allowing the Fentanyl pain patch to become hot, which increases the delivery of Fentanyl through the skin.

If you or a loved one has suffered serious or fatal illness from misuse of Duragesic or Fentanyl pain patches, you may be entitled to compensation. Contact a Duragesic attorney at Cappolino Dodd Krebs LLP at 1-800-460-0606. An experienced Fentanyl attorney will be able to evaluate if you are eligible to seek compensation.

          Medical researcher Dr. Dennis Mangano concluded in a recent report that the delayed recall of the Bayer drug Trasylol caused the death of approximately 22,000 people. Trasylol is a drug that is used during open-heart surgery to stem bleeding and as many as one third of all heart bypass patients in the United States were given Trasylol during the peak of its use by doctors.
          Dr. Mangano’s study (published in January of 2006) showed that the medicine can cause kidney failure and increased death in its patients. The Food and Drug Administration advisory panel discussed the study and its findings at their September 2006 meeting but declined to recall Trasylol. Dr. Mangano alleges that this is at least in part because Bayer did not tell the FDA the serious side effects of Trasylol had also been found in Germany.
          Trasylol was finally recalled last November, and for many the delay was a death sentence. If the FDA had voted to recall Bayer’s Trasylol at that meeting in 2006, or if Bayer had issued a voluntary recall in light of the negative findings, more than 20,000 lives could have been saved. Bayer is currently facing product-liability lawsuits from victims and families of victims of Trasylol. If you or someone you love has been exposed to Trasylol, contact the lawyers at the law firm of Cappolino Dodd  Krebs LLP at 1-800-460-0606 for legal counsel as soon as possible.

A second voluntary recall has been issued for Fentanyl pain relief patches. 14 lots of Actavis generic Fentanyl CII were recalled because of a fold-over defect that could possibly expose patients and caregivers to Fentanyl gel.

Exposure to Fentanyl gel may result in serious or fatal adverse effects, such as respiratory depression and overdose.

The Actavis recall follows the recall of all 25 microgram/hour PriCara and Sandoz Fentanyl patches. The PriCara and Sandoz Fentanyl patches were recalled because of a cut along the side of the Fentanyl gel reservoir, possibly causing exposure to the Fentanyl gel.

The lots affected by the recall include 25-, 50-, 75-, and 100-microgram/hour strengths. The lot numbers are:

• 27261 (expiration date 5/09)
• 27317 (expiration date 5/09)
• 27318 (expiration date 6/09)
• 27319 (expiration date 6/09)
• 27391 (expiration date 6/09)
• 27409 (expiration date 6/09)
• 27475 (expiration date 7/09)
• 27476 (expiration date 6/09)
• 27488 (expiration date 6/09)
• 27514 (expiration date 7/09)
• 27536 (expiration date 7/09)
• 27537 (expiration date 8/09)
• 27538 (expiration date 8/09)
• 27545 (expiration date 7/09)

Damaged patches should not be used under any circumstances. Damaged or cut fentanyl patches should be stored in a safe, tightly-sealed container, out of reach of children. To avoid exposure to the fentanyl gel, do not handle the patch directly. Do not re-use a container in which you stored damaged or cut fentanyl patches.

If you or a loved one has suffered serious illness or death due to exposure to Fentanyl, contact a Fentanyl pain patch attorney at Cappolino Dodd Krebs LLP at 1-800-460-0606. An experienced Fentanyl pain patch lawyer will be able to evaluate if you are eligible to seek compensation.