The Dangers of High Caffeine Drinks – 5 Hour Energy and Monster Energy
According to the Substance Abuse and Mental Health Services Administration, more than 13,000 emergency room visits in 2009 alone were associated with energy drinks. The FDA is looking into the death reports that cited 5-Hour Energy.
The FDA also reports that it has over 90 report associating this one drink with serious injuries like convulsions, heart-attacks and spontaneous abortions. Another energy drink called Monster Energy has been implicated in five deaths reported to the FDA. You can see a recent news article about this subject here.
High energy drinks often contain a mixture of substances, with little information given about how these ingredients might react with each other. The main is ingredient is typical a high dose of caffeine, but sometimes the exact amount is not disclosed in the product labeling. Since these report have been coming in for years now, Levin Papantonio is investigating why the makers of these products did not do more to warn customers about the risk of the dangers. If you or a loved one was injured or killed from a Caffeinated Energy drink, give us a call or send us an email from this site and we will see if we can help you with a claim for due compensation.
FDA Warning Letters issued to four makers of caffeinated alcoholic beverages.
These beverages present a public health concern.
The U.S. Food and Drug Administration today warned four companies that the caffeine added to their malt alcoholic beverages is an “unsafe food additive” and said that further action, including seizure of their products, is possible under federal law.
The companies receiving Warning Letters and their products are:
• Charge Beverages Corp.: Core High Gravity HG, Core High Gravity HG Orange, and Lemon Lime Core Spiked • New Century Brewing Co., LLC: Moonshot • Phusion Projects, LLC (doing business as Drink Four Brewing Co.): Four Loko • United Brands Company Inc.: Joose and Max.
FDA’s action follows a scientific review by the Agency. FDA examined the published peer-reviewed literature on the co-consumption of caffeine and alcohol, consulted with experts in the fields of toxicology, neuropharmacology, emergency medicine, and epidemiology, and reviewed information provided by product manufacturers. FDA also performed its own independent laboratory analysis of these products.
“FDA does not find support for the claim that the addition of caffeine to these alcoholic beverages is ‘generally recognized as safe,’ which is the legal standard,” said Dr. Joshua M. Sharfstein, Principal Deputy Commissioner. “To the contrary, there is evidence that the combinations of caffeine and alcohol in these products pose a public health concern.”
Experts have raised concerns that caffeine can mask some of the sensory cues individuals might normally rely on to determine their level of intoxication. The FDA said peer-reviewed studies suggest that the consumption of beverages containing added caffeine and alcohol is associated with risky behaviors that may lead to hazardous and life-threatening situations.
The agency said the products named in the Warning Letters are being marketed in violation of the Federal Food, Drug, and Cosmetic Act (the FFDCA). Each Warning Letter requests that the recipient inform the FDA in writing within 15 days of the specific steps that will be taken to remedy the violation and prevent its recurrence. If a company does not believe its products are in violation of the FFDCA, it may present its reasoning and any supporting information as well.
If the FDA believes that the violation continues to exist, the agency may pursue an enforcement action that could include seizure of the products or an injunction to prevent the firm from continuing to produce the product until the violation has been corrected.
FDA’s action today follows a November 2009 request to manufacturers to provide information on the safety of adding caffeine to their products.
FDA is aware that on November 16, Phusion Projects, LLC, the maker of Four Loko, announced its intention to remove caffeine and other stimulants from its drinks. FDA views this announcement as a positive step. FDA has not yet heard officially from the company about this announcement, including how quickly it will remove present product from circulation and how quickly it will reformulate its product. FDA intends to work with Phusion Projects, LLC and the other manufacturers to assure their products meet safety standards.
We have decades of working with individuals and families affected by dangerous products. We engage life care planners to develop comprehensive plans to forecast what our clients will likely need in terms of care for the rest of their lives. We engage economic experts to provide present money value opinions to the medical needs as well as the loss of earning capacity that our clients have suffered and will likely experience in the future. A deep understanding of the economic damages of our clients allows us to seek a full measure of damages from those at fault.
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