FDA Issues Ozempic Update After Users Cite “Severe” Gastrointestinal Issues

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FDA Issues Ozempic Update After Users Cite “Severe” Gastrointestinal Issues
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Amid complaints of 'severe' gastrointestinal side effects from patients, the FDA has issued an update about the weight-loss drug Ozempic.

that the FDA has decided to update the label for Ozempic to acknowledge one specific gastrointestinal disorder: Ileus. According to the news outlet, the labels of Mounjaro and another sister drug, Wegovy, already acknowledged reports of some users developing this condition—and now Ozempic's label has been updated to say the same.

"Ileus is the medical term for lack for movement somewhere in the intestines that leads to a buildup and potential blockage of food material," HRS explains , noting that this condition is commonly related to gastroparesis."An ileus can lead to an intestinal obstruction. This means no food material, gas, or liquids can get through.", the FDA does not directly blame Ozempic or Novo Nordisk for users developing ileus, however. Instead, the agency simply acknowledges that there have been some reports of people experiencing this gastrointestinal disorder following their use of the main medication used in Ozempic.

"The following adverse reactions have been reported during post-approval use of semaglutide, the active ingredient of Ozempic," the updated label states."Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

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