Have You Been Deceived Into Buying HCG Diet Pills?

One of the most difficult issues consumers trying to losing weight face is purchasing a diet product that works. Unfortunately, many unscrupulous marketers deceive consumers into buying unproven or outright worthless products based on bogus weight loss claims. One of the more egregious scams that have come to light recently concerns HCG.  In fact, the FDA sent letters to several HCG diet-product companies, warning them that HCG weight-loss drugs have not been approved by FDA, and that the claim that HCG can help in weight loss is unsupported.

HCG, or human chorionic gonadotropin, is a hormone produced by the human placenta during pregnancy. HCG is approved by FDA as a prescription drug for the treatment of female infertility, and other medical conditions. However, it is not approved for weight loss. Nonetheless, may HCG marketers claim that HCG can “reset your metabolism,” change “abnormal eating patterns,” and cause one to two pounds of weight loss per day. Typically, these products come with a very low calorie diet, and any weight loss is attributable to the diet, not HCG.

 

If you or someone you know purchased a HCG weight loss product, contact us to discuss your legal options.

Sibutramine Is A Dangerous Drug

Sibutramine is a controlled substance drug known as an oral anorexiant. It is a form of medication known as an appetite suppressant, which works by acting on the appetite control centers in the brain to decrease appetite. It was previously marketed and prescribed by physicians as part of the treatment for weight loss, and was used in combination with a reduced calorie diet and exercise to help people who are overweight lose weight and maintain their weight loss.

In 2008, the United States Food and Drug Administration issued an alert to consumers naming 27 different products marketed as dietary supplements for weight loss that contained illegal and undisclosed amounts of sibutramine. By 2010, the manufacturer of sibutramine had withdrawn the drug from the market altogether after study showed an increased risk of stroke and other cardiovascular problems in persons who were prescribed the medication. The manufacturer had performed a study at the request of the Food and Drug Administration, which ultimately demonstrated a 16% increase in the risk for serious cardiovascular events such as heart attack, stroke, myocardial infarction, and death. Sibutramine is not supposed to be prescribed or sold in the United States, and if “off the market.”

Unfortunately, sibutramine continues to appear on the market, mostly in products that are marketed as dietary supplements for weight loss. Just recently, on October 18, 2011, the Food and Drug Administration issued alerts to consumers advising them not to use or purchase several products that were found to contain sibutramine. The agency issued alerts advising consumers to avoid the products known as "Magic Slim,” “Advanced Slim 5” and “Magic Slim Tea” because they were all found to contain the illegal drug sibutramine.

It is illegal and extremely dangerous for manufacturers of so-called "dietary supplements" to mix sibutramine in their products, and it is unfortunate that some unscrupulous manufacturers continue to do so.  If you or someone you know has been injured by sibutramine, please contact us to discuss your legal rights.

Svelte 30 and Extenze: Unapproved Drugs Sold As Dietary Supplements Lead To FDA Recall

The Food and Drug Administration ("FDA") recently required the manufacturers of two purported "dietary supplements" to recall their products because they contained unapproved drug ingredients.  The products, Svelte 30 (manufactured by Svelte 30 Nutritional Consultants) and Extenze (manufactured by Biotab Nutraceuticals, Inc.), were found to contain sibutramine.  Although sibutramine is an FDA-approved drug used as an appetite suppressant for weight loss, it is a controlled substance, which was withdrawn from the market in October 2010 for safety reasons.  Several lots of Extenze also were found to contain prescription drugs used to treat erectile dysfunction.

Products containing a drug ingredient must be approved by the FDA.  As a result, manufacturers sometimes seek to market their products as "dietary supplements", even tough they contain a drug ingredient, to escape the expensive and rigorous FDA approval process.  Unlike drugs, manufacturers may market dietary supplements simply upon giving the FDA notice within thirty days after they start marketing the product.  If the FDA does not formally object, the manufacturer may continue to market the product without the FDA having made any determination as to its safety or efficacy.

Because the FDA has not approved Svelte 30 and Extenze, their safety and effectiveness are unknown.  In fact, their drug ingredient, sibutramine, is known to substantially increase blood pressure or pulse rate in some people and may be especially risky for those with a history of heart problems or stroke.  Additionally, drugs like sibutramine, which are used to treat erectile dysfunction, may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels.

The FDA product recall includes the following:

  • Svelte 30 Orange & Gray Capsules:  Svelte is marketed as a natural herb for weight loss and is packaged in plastic bottles containing 30 capsules per bottle.  The recalled products have UPC numbers from 04-3000 to 04-5999, manufacturing date of 10/22/2010, and expiration date of 10/21/2012.
  • Extenze Tablets:  Two lots of counterfeit products sold nationwide are packaged as a card of four packs (lot 0709241) and a box of 30 tablets divided into two 15-tablet blister packs (lot 0509075).  It is possible that there may be other Extenze counterfeit products on the market that have not yet been identified.

If you, or someone you know, has purchased or used Svelte 30 or Extenze containing sibutramine, please contact us to discuss your legal rights.

 

Beware Of Diet Scams

Who wouldn’t want to lose weight without dieting or exercise?  The weight loss industry makes billions of dollars each year by preying upon our desire to lose those extra pounds.  However, physicians and other health experts caution that there is no “magic bullet” when it comes to weight loss.  And many health experts recommend that safe diets require a loss of no more than 2 pounds per week.

Despite these recommendations, the Internet is rife with ads promising to “Lose 25 Pounds in 2 Weeks” and supposed testimonials proclaiming, “I lost 36 pounds in 1 month.”  Consumers should beware of these claims.  In fact, the Federal Trade Commission (“FTC”) has issued guidelines for consumers warning them to “think twice before wasting money on products that make any of the following false claims”:

Lose weight without diet or exercise!

Lose weight no matter how much you eat of your favorite foods!

Lose weight permanently! Never diet again!

Block the absorption of fat, carbs, or calories!

Lose 30 pounds in 30 days!

Everybody will lose weight!

Lose weight with our miracle diet patch or cream!

If you or someone you know has been the victim of a diet scam, please contact us to discuss your legal options.

FDA Warns Consumers To Stop Using Hydroxycut Products

In a post published back in January 14, 2009, this blog discussed the fact that the Food and Drug Administration (“FDA”) had identified a number of weight loss products as containing potentially dangerous ingredients. Recent events have shown the warnings to be justified.

The FDA has warned consumers to immediately stop using the Hydroxycut line of weight loss products, citing reports of death due to liver failure and other serious health problems. The Hydroxycut brand includes pills, drinks and powders marketed to increase energy, burn calories and fat, and control appetite. Hydroxycut products have been widely sold at national chain stores, including GNC and Vitamin Shoppe. The FDA has received 23 reports of significant health problems in persons using Hydroxycut products ranging from jaundice and elevated liver enzymes (an indication of potential liver injury) to liver damage requiring a liver transplant. According to the FDA, symptoms of liver injury include nausea, vomiting, light-colored stools, excessive fatigue, weakness, stomach or abdominal pain, itching and loss of appetite. Other health problems associated with the use of Hydroxycut products reported to the FDA include seizures, cardiovascular disorders and a type of muscle damage known as rhabdomyolysis that can lead to other serious health problems, including kidney failure.

 If you have purchased and used a Hydroxycut product, please contact us to discuss your legal options.