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Byetta®-related cases of hemorrhagic or necrotizing pancreatitis have been reported ever since this medical device was introduced in the United States in 2005 and in the UK in 2006. In 2007, the FDA issued an "Information for Healthcare Professionals" regarding the link between Byetta® (exenatide) and pancreatitis, and within another 12 months the FDA received reports of six more cases of Byetta®/pancreatitis cases.
In fact, nearly 400 Byetta®-user cases of pancreatitis were reported worldwide as of February 2009, according to a newsletter published by the MRHA (Medicines and Healthcare Regulatory Agency), the UK counterpart to the FDA. The number of Byetta® cases of pancreatitis continues to grow, and many lawsuits have been initiated regarding this deadly side effect of Byetta®.
Byetta® is prescribed by healthcare providers around the world to adult patients with type 2 diabetes. The injectable Byetta® pens are used twice a day to control a diabetic's glucose (blood sugar) level, before the morning and evening meals. The makers of Byetta® (San Diego-based Amylin Pharmaceuticals and Indianapolis-based Eli Lilly & Co.) explain that Byetta® works "at least four different ways" by:
Pancreatitis cases range from early-onset, relatively easily treated situations to severe, emergency cases that can be fatal. The inflammation of the pancreas can cause serious and uncontrollable bleeding resulting in death. The first U.S. Byetta® lawsuit filed by a Byetta® patient alleged that Byetta® maker Amylin failed to adequately warn prescribing physicians of:
Essentially all of the Byetta® cases and lawsuits since then have touched on these same points.
If you suspect that medical problems that you or your loved one experienced after starting Byetta® treatment may be actionable, talk to a Byetta® lawyer who represents victims of dangerous drugs and medical devices. He or she can discuss your circumstances with you in a no-cost, no-obligation consultation.
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