| Subject: | FDA Issues Postmarketing Safety Information about Byetta (exenatide) |
| Category: | Food and Drug Administration (FDA)
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| Published: | Wed, 17 Oct 2007 - 10:00 am |
| Audience: Endocrinologists, other healthcare professionals, consumersThe FDA has reviewed 30 postmarketing reports of acute pancreatitis in patients taking Byetta (exenatide), a drug used to treat adults with type 2 diabetes. An association between Byetta and acute pancreatitis is suspected in some of these cases. Amylin Pharmaceuticals, Inc. has agreed to include information about acute pancreatitis in the PRECAUTIONS section of the product label. According to the FDA, healthcare professionals... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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