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ELIDEL AND PROTOPIC LINKED TO CANCER RISK

Elidel and Protopic are creams prescribed to children and adults to treat the skin disease eczema. In January 2006, the FDA announced that the drugs would carry a black box warning alerting patients to the possible increased risk of non-Hodgkins lymphona (lymph node cancer) or skin cancer from the use of Elidel and Protopic.

In 2005, reports were released in which the medications were shown to cause skin cancer in mice. There has not been a direct link between Elidel or Protopic use and cancer established in humans, but rare reports of cancer in patients using Elidel or Protopic have been documented.

In February 2005, the FDA Pediatric Advisory Panel recommended that major black box warnings be added to the Elidel and Protopic labels informing of the potential risk of the development of cancer. A public health advisory was issued in March 2005 to alert physicians to the possible cancer risk.

Case Background

Elidel (picmecrolimius) cream and Protopic (tacrolimus) cream are prescribed for eczema patients as an alternative to topical steroids. Elidel and Protopic work to selectively reduce the inflammatory symptoms of eczema, which is also known as atopic dermatitis.

Eczema is a chronic, itchy inflammation of the upper layers of the skin. It most commonly occurs on the face, neck, upper chest, shoulders, and the elbows and knees. Elidel and Protopic are prescribed for use in children 2 years of age and older.

Elidel and Protopic are calcineurin inhibitors, which is also known as an immunosuppressants. Immunosuppressants inhibit activity of the immune system.

Health Risks and Symptoms

The only method for avoiding possible cancer risk is to refrain from continuous, long-term use of Elidel or Protopic. The application of the cream should be limited to only the affected areas of the skin.

Elidel and Protopic should only be used if other treatments have failed in treating the eczema. The use of Elidel or Protopic should end as soon as the eczema resolves itself, and patients should be re-evaluated if the symptoms of eczema continue for more than six weeks.

The risk of cancer increases as the dose of the drug increases, so only the lowest effective dose should be used. Patients with a weakened immune system should not use Elidel or Protopic.

Do I Qualify for an Elidel or Protopic Lawsuit?

If you or a member of your family has taken Elidel or Protopic, then you may qualify for a lawsuit claim. Thousands of people have already filed claims.

In America today there are thousands of mass lawsuits and billions of dollars in unclaimed monies available for victims. If you have been wronged by a major corporation, you may be entitled to compensation for treatments and pain and suffering.

 

 
If you believe you have been wronged, take action to protect your rights.
 
Fill out this form or call 1.800.387.4262 if you need additional information or want to discuss a potential claim with an attorney. All inquiries are kept strictly confidential.

If the inquiry is accepted for further review, you will receive a prompt response (usually the same day or by the next business day). Local counsel may be used for this matter.

 
Claim Evaluation Form
Name  

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  State

 

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Phone

 

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*please include a phone number

Did you or a loved one take Elidel or Protopic and suffer any of the following health problems?:

Skin cancer
Lymph node cancer
Other side effects (describe below)
When did you or a loved one take Elidel or Protopic?
What health effects did you suffer?



I agree that the above is not a request for legal advice and that I am not forming an attorney client relationship. Since this matter may require advice regarding my home state, I agree that local counsel may be contacted for referral of this matter.



 
 
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