Hydroxycut Lawsuit Class Action

Hydroxycut Class Action Lawsuit Hydroxycut Lawsuit

Hydroxycut Class Action Lawsuit
Hydroxycut Lawsuit


The hydroxycut weight loss and bodybuilding supplement has been linked to liver damage and permanent liver injury, if you are taken hydroxycut and expirienced liver problems you most likely have a lawsuit. 

To contact the Hydroxycut Lawsuit Claim Center and lead attorney for these cases for doihavealawsuit.com for a free case evaluation at no cost. complete the case review form found here on the doihavealawsuit.com


In a case that would have puzzled some of the nation's most prominent doctors,


A 33 year old woman arrived at the Yale New Haven emergency room with complaints of extreme fatigue , dark urine and a yellowing of her skin. Hospital lab test quickly identified the problem as acute liver inflammation.


A liver specialist at Yale, Joseph Lim, began to investigate. He noted that the woman had been taking Hydroxycut supplements for weight loss for two weeks. Several reports in the medical literature had linked Hydroxycut (which is used for both bodybuilding and weight loss) to liver damage.

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Hydroxycut Class Action Lawsuit Attorney

 


When his patient stopped taking the popular supplement, she improved, leading Lim to finger the product.


On May 1, the Food and Drug Administration warned consumers to stop taking Hydroxycut, which had been linked to liver damage and jaundice.


These complaints include one liver transplant and one fatality, a 19-year-old man from the southwestern United States, the FDA said.


Iovate Health Sciences, the Ontario-based manufacturer, voluntarily recalled 14 Hydroxycut products (two, Hoodia and Hydroxycut Cleanse, were not recalled because they contain different ingredients).


An Iovate spokeswoman referred a reporter to a statement on the company's Web site, which said that few adverse reports had surfaced compared to the numbers of Hydroxycut users, and that the company issued the recall from "an abundance of caution."


Lim said he supported the FDA's warning because the supplements are widely used and have undergone far less scrutiny than many people realize.
Dietary supplements are not tested by the FDA for safety or efficacy. The FDA relies on consumers, doctors, or manufacturers to alert them to health issues, but this can take time.


An estimated 15 percent of the U.S. population use over-the-counter weight-loss supplements, and Hydroxycut marketing declares it to be "America's No. 1 selling weight-loss supplement" in the United States.
The company sold more than nine million bottles of Hydroxycut in 2008, executives told the FDA.


Yet it remains unclear how many people Hydroxycut may have injured or even which of its ingredients are dangerous.


A visit to a local drug store showed that while Hydroxycut had been pulled from the shelves, many of its ingredients were widely available in other products still for sale. The FDA's Vasilios Frankos, director of the Division of Dietary Supplements Program, said last month that the agency was investigating those ingredients and other products that contain them.

Attorneys for doihavealawsuit.com  have also been on the forefront in investigating these harmful products.


"The people have a right to file a hydroxycut lawsuiit"


The Hydroxycut ingredient that shares the product's name, hydroxycitric acid or HCA, has a long history. Drugmaker Hoffmann-La Roche tried to turn HCA into a weight-loss drug in the mid-1970s, but abandoned the research even before human testing because of toxicities in animals, said company spokesperson Darien Wilson. HCA is derived from the rind of a pumpkinlike tropical fruit that grows on the Garcinia cambogia tree.


Besides HCA, Lim said, two other ingredients could be toxic: the mineral chromium and Camellia sinensis, the tea plant. When ingested, both have been implicated in the medical literature as potential liver toxins.


So just recalling Hydroxycut hasn't fully protected the public, said Ano Lobb, an independent public health researcher for academic, nonprofit, and government entities. The hydroxycut lawsuits filed by attorneys affiliated with doihavealawsuit.com have steadily increasing as our lawyers gather more information each day.


"Hydroxycut is dangerous, so [consumers] look down the shelf and grab another weight-loss supplement," said Lobb, who a few weeks before the FDA's announcement published an article about the links between Hydroxycut and liver damage. "The message should be that [weight-loss and bodybuilding] supplements are some of the most dangerous."


Lobb became interested in Hydroxycut after seeing some of its ubiquitous advertisements featuring a formerly chubby, currently ripped medical doctor. "They kept citing clinical evidence that the product works. I wanted to know what that evidence was," Lobb said.


Hydroxycut packaging claims it increases energy and burns calories with "clinically proven" ingredients. Lobb found that the weight-loss studies yielded inconsistent results at best. "Besides the industry-funded studies, which should be viewed with some skepticism, they tended to be on animals," he said.


"There should be more evidence out there before it goes to market," Lobb added. Now, the burden "falls to the consumer."


Considering the supplement's popularity and the number of events reported, the FDA called the liver complications "relatively rare." However , liver damage can lead to death or other less harmful long term injuries that require medical attention and legal representation in these recall lawsuits.


However, most experts agree that adverse events are dramatically underreported. A doctor or consumer won't always connect a supplement to a medical condition. And patients often fail to tell their doctors about supplement use.


Even then, the chances that a case will reach the FDA are slim. An FDA-commissioned study from 2001 found the FDA received only about 1 percent of supplement-related adverse-event reports.


The one Hydroxycut-related death cited by the FDA took two years to reach the agency. Such a delay isn't unusual, said Linda Katz, the FDA's interim chief medical officer for its Center for Food Safety and Applied Nutrition.


The FDA's decision to warn against Hydroxycut was also prompted by four cases in the medical literature reporting that Hydroxycut had caused liver toxicity.


The case reports - Lim wrote the most recent - follow a similar course: a sudden illness, sometimes requiring hospitalization, in the weeks or months after starting Hydroxycut, followed by improvement after stopping the supplement.


But not all liver disease follows this pattern.


A class-action lawsuit against the makers of Hydroxycut and we continue to assist new victims of this supplements liver damaging side effects each day.
Stephen Snuffer, 59, a Mormon, was shocked to learn he had liver disease after a health insurance screening in December.


Hydroxycut had been part of Snuffer's daily routine for five years.


An independent insurance agent and author who lives on his own mountain in Cool Ridge, W. Va., Snuffer had assumed anything sold at GNC was healthy. "I used it as a supplement to prevent me from being hungry," he said. "I don't have time to stop and eat on the road."


Snuffer's liver enzyme levels indicate liver damage, but are far from those generally associated with acute liver toxicity. Even so, they are high enough to make individual insurance too expensive.


If cases such as Snuffer's can be attributed to Hydroxycut, the number of victims could rise substantially and thus result in more consumers filing hydroxycut lawsuits or contacting us for lead hydroxycut lawsuit attorney class action case information.

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