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Pharmaceutical Litigation

Byetta®

Manufacturer: Amylin Pharmaceuticals, Inc. & Eli Lilly & Co.


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Byetta

The FDA is alerting health care professionals that Byetta® may be associated with acute pancreatitis in some patients.  Byetta® is administered by a twice a day injection to treat type two diabetes.  More than 700,000 patients have used the drug since it was released in 2005.

The FDA has reviewed 30 reports of individuals taking Byetta® and developed acute pancreatitis.  21 of those patients were hospitalized, five of them with serious complications.  22 of these individuals improved after discontinuing the drug.

Symptoms of acute pancreatitis are persistent and severe abdominal pain possibly accompanied by vomiting.   

If you or someone you know has sustained acute pancreatitis or other damages while taking Byetta®, please contact us to discuss your rights,  www.816LAWFIRM.com  or call us toll-free at 1-800-305-7552.

Call Peterson & Associates today & Click Here.

Byetta

For more information:
Pharmaceutical Litigation
Prescription Injury FAQs
Pharmaceutical Legal Glossary


Recent Byetta Headlines

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>>  Weather delays US FDA action on long-acting Byetta - Reuters... - Thu, 25 Feb 2010
>>  Taspoglutide may have the highest potential of sales amongst GLP-1 - G... - Wed, 10 Mar 2010
>>  PDUFA date for Exenatide Approaching (Nasdaq:AMLN), (NYSE:LLY) - FavSt... - Thu, 11 Mar 2010


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