Zyprexa

Zyprexa is an atypical anti-psychotic manufactured by Eli Lilly. The FDA approved Zyprexa in 1996 to treat schizophrenia and bi-polar disorder.

Zyprexa side effects include weight gain, failure to regulate body temperature, uncontrollable movements in the face and extremities, and gastrointestinal problems. The most serious side effects of Zyprexa include Neuroleptic Malignant Syndrome, tardive dyskinesia, and diabetes.

In 2002, a Duke University study revealed an incredible risk of adult onset diabetes presented to patients who were prescribed Zyprexa. 23 patients in this study died. In response to this, the FDA ordered Eli Lilly to include a stronger diabetes risk warning on Zyprexa product information.

Zyprexa is a dangerous drug but remains on the market. Zyprexa presents very real and possibly fatal side effects, yet continues to be prescribed in America.

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Home Recent FDA Recalls Other Dangerous Drugs The FDA Approval Process Frequently Asked Questions FDA Recall News About the Firm What is Product Liability? Contact Us	Zyprexa Zyprexa is an atypical anti-psychotic manufactured by Eli Lilly. The FDA approved Zyprexa in 1996 to treat schizophrenia and bi-polar disorder. Zyprexa side effects include weight gain, failure to regulate body temperature, uncontrollable movements in the face and extremities, and gastrointestinal problems. The most serious side effects of Zyprexa include Neuroleptic Malignant Syndrome, tardive dyskinesia, and diabetes. In 2002, a Duke University study revealed an incredible risk of adult onset diabetes presented to patients who were prescribed Zyprexa. 23 patients in this study died. In response to this, the FDA ordered Eli Lilly to include a stronger diabetes risk warning on Zyprexa product information. Zyprexa is a dangerous drug but remains on the market. Zyprexa presents very real and possibly fatal side effects, yet continues to be prescribed in America. For more information, please visit us at www.levinlaw.com Home \| Recent FDA Recalls \| Other Dangerous Drugs \| The FDA Approval Process \| Frequently Asked Questions \| FDA Recall News \| About the Firm \| Links \| Site Map \| Contact Us Levin, Papantonio, Thomas, Mitchell, Echsner & Proctor, P.A. 316 South Baylen Street, Suite 600 Pensacola, FL 32502-5996 toll free: (888) 435-7001, (850) 435-7000 fax: (850) 497-7057 Copyright Levin, Papantonio, Thomas, Mitchell, Echsner & Proctor. Pensacola, Florida Personal Injury Attorneys. All Rights Reserved. Disclaimer: Levin, Papantonio, Thomas, Mitchell, Echsner & Proctor Pensacola, dangerous drug lawyers provide the information in this web site for informational purposes only. The information does not constitute legal advice. The use of this site does not create an attorney-client relationship. Further communication with our personal injury attorneys through the web site and e-mail may not be considered as confidential or privileged. Please contact our defective pharmaceutical and medical device attorneys for a free evaluation of your claim.	Defective Drugs Accutane Bextra Crestor Cylert Duragesic / Fentanyl Neurontin Vioxx Zyprexa Defective Medical Devices Baxter Infusion Systems Guidant Heart Defibrillators