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Pharmaceutical Litigation

Byetta®

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


More Information
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

>>  Amylin Rises on Byetta Sales Data - TheStreet.com... - Mon, 17 Nov 2008
>>  Feds deal a setback to new Byetta version - Indianapolis Star... - Thu, 06 Nov 2008
>>  Amylin Slices Payroll by 340 Following Setbacks by Byetta - TMCnet... - Wed, 12 Nov 2008
>>  Byetta uptick, Icahn news boost Amylin - FiercePharma... - Tue, 18 Nov 2008
>>  Is Byetta the Next Rezulin or Avandia – Yet Another Promising Drug ...... - Wed, 19 Nov 2008


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Recall News
DIGITEK RECALL!

The FDA has recalled all Digitek tablets after the discovery of manufacturing defects.  Individuals taking Digitek tablets may suffer from an illness known as Digitalis Toxicity and various other symptoms.  This manufacturing defect may cause serious health problems, and even death.   

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