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STRATTERA LINKED TO SUICIDIAL THOUGHTS AND BEHAVIORS IN CHILDREN AND ADOLESCENTS

Reports of suicide attempts and suicidal thoughts by adolescents and children taking the hyperactivity drug Strattera (atomoxetine) became public in 2006. Other children have suffered side effects including fits, palpitations, and liver disorders. Safety warnings will be placed on the packaging to indicate that suicidal thoughts/attempts may be associated with the use of Strattera.

In a report made public in February 2006, 20 patients reportedly committed suicide after taking Strattera, and 63 others attempted suicide. Eli Lilly, the manufacturer of Strattera, revealed in September 2005 that some children taking Strattera had experienced suicidal thoughts and behavior.

Strattera has also previously been linked to death from heart problems and liver problems. In February 2006, and FDA advisory committee recommended that Strattera carry a major black box warning of heart attacks and strokes. The FDA voiced concerns about Strattera last year, but did not address these concerns until just recently.

Case Background

Strattera is a daily medication that is prescribed to children with Attention Deficit Disorder (ADD) and Attention Deficit Hyperactivity Disorder (ADHD). It works to increase they body's production of dopamine, which allows the children to be better able to focus. Strattera is approved to treat ADD and ADHD in children as well as Adult ADD. It has not been tested in children under six years of age, however.

Strattera is a norepinephrine reuptake inhibitor, and is the only non-stimulant medication approved by the FDA for treating ADD and ADHD.

ADD and ADHD are marked by impulsivity and inattention, and ADHD also involves hyperactive behavior.

Health Risks and Symptoms

If a child or adolescent is observed to be suffering from suicidal thoughts or behavior, they should immediately be evaluated by a physician. The use of Strattera may be temporarily or permanently discontinued.

Likewise, if symptoms of heart or liver damage are observed, a physician may discontinue the use of Strattera and treat the symptoms of the organ damage. Liver damage treatment may involve the prescription of diuretics and vitamins, and if an infection occurs, antibiotics may be prescribed. In severe cases, a liver transplant may be needed.

Do I Qualify for an Strattera Lawsuit?

If you or a member of your family has taken Strattera, 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 Strattera and suffer any of the following health problems?:

Suicidial thoughts/behaviors
Attempted suidice
Liver damage
Heart problems
Other side effects (describe below)
When did you or a loved one take Strattera?
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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