Januvia’s Link to Pancreatic and Thyroid Issues: Januvia Safety Concerns

A relatively new class of drugs known as sitagliptin includes the brand name Januvia and is used in the treatment of type 2 diabetes. Januvia—along with others in the same class—has been shown in some studies to bring significant risks to patients taking the drug. Januvia blocks or inhibits DPP-4 in the body, allowing the patient’s system to better control glucose levels as well as increasing the amount of insulin produced by the pancreas when the blood sugar is high. These DPP-4 blockers can also reduce the amount of sugar produced by the liver when the body does not need the excess. 

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Januvia Class Action Lawsuits vs. Januvia MDL

Januvia, a drug approved in 2006 by the FDA to be used in the treatment of Type 2 diabetes, has been found to bring a risk of pancreatitis, pancreatic cancer and thyroid cancer among users. Reports of 88 serious cases of pancreatitis were sent to the FDA between the time Januvia was approved and 2009. Of these 88 cases, over half resolved when Januvia was discontinued. At least one-fifth of the patients had only been taking Januvia for a month or less and 75% of the patients required hospitalization. 

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Januvia Legal Help and What to Look for in a Januvia Attorney

As more time passes, it appears more people are coming forward to say they have been harmed by a drug they believed to be safe—in this case, Januvia.  Januvia, manufactured by Merck & Co., is a drug used in the treatment of Type 2 diabetes. Januvia controls blood sugar when the body is unable to do so and is meant to be used in conjunction with diet and exercise. Sitagliptin, the active ingredient in Januvia, works by inhibiting an enzyme known as DPP-4 which breaks down the hormones sending signals to the pancreas to produce more insulin. After FDA approval in 2006, scores of adverse reports were submitted to the FDA by Januvia users and recent studies show a definite link between Januvia and pancreatitis, pancreatic cancer and thyroid cancer. 

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Frequently Asked Questions Regarding Januvia

Januvia is a drug manufactured by Merck & Co. to treat Type 2 diabetes, gaining FDA approval in 2006. Januvia contains sitagliptin which inhibits the DPP-4 enzymes in the body, destroying glucagon-like peptide-1 which reduces blood glucose levels. Following a meal, incretin hormones are released from the intestine; these hormone levels are then increased in the bloodstream in patients taking Januvia. When the active ingredient found in Januvia blocks DPP-4, the body can better handle glucose levels, increasing the amount of insulin the pancreas produces when excessive blood sugar demand such an increase. During times when the body does not need the excess liver sugars, the DPP-4 will also lower those sugars. When combined with diet and exercise Januvia can significantly improve blood glucose levels in those with Type 2 diabetes. 

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Actos Lawsuits Part One: Failure to Warn and a Possible Cover Up

Nearly thirteen years ago a new diabetic drug, Actos, was approved for the treatment of Type 2 diabetes. Takeda, the Japanese manufacturer of Actos collaborated with Eli Lilly to release the drug in the United States at the time. At the same time Actos was approved, a close competitor, Avandia, was also approved.
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