Why is Hydroxycut banned?
In 2004, Hydroxycut products containing ephedra were withdrawn from use in the United States because of cardiovascular risks and in 2009 because of hepatotoxicity.Apr 12, 2018
Specialist journal
In 2004, Hydroxycut products containing ephedra were withdrawn from use in the United States because of cardiovascular risks and in 2009 because of hepatotoxicity.Apr 12, 2018
On May 1, 2009, the U.S. Food and Drug Administration (FDA) issued a warning to consumers to stop using Hydroxycut products, due to 23 reports of serious health problems associated with the use of Hydroxycut, and at least one death, and to destroy any product that they may possess.
The agency said that while adverse events were rare, they were still cause for concern. Hydroxycut products later returned to the market with different ingredients, including herbs. While the current ingredients are deemed safe, Hydroxycut has continued to be linked to a few health problems.
Is Hydroxycut Safe? Hydroxycut's maker, Iovate Health Sciences International, says it puts raw ingredients through extensive quality assurance procedures. In 2009, Iovate recalled Hydroxycut after the FDA got reports of liver problems, seizures, and a muscle-damaging condition called rhabdomyolysis.
The 23 reports of adverse effects include liver damage, elevated liver enzymes (which indicates potential liver damage) and liver damage requiring a transplant. A 19-year-old man died after using Hydroxycut. "The death occurred in 2007," Katz says, "and was reported to the agency at the end of March 2009."
Since the Hydroxycut products are not approved, prescription drugs, there was little published regarding a potential risk if mixed with other medications.
Iovate has agreed to recall Hydroxycut products from the market. The FDA has received 23 reports of serious health problems ranging from jaundice and elevated liver enzymes, an indicator of potential liver injury, to liver damage requiring liver transplant. One death due to liver failure has been reported to the FDA.
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