Charlottesville Personal Injury Lawyer - supplements

Supplements - More Dangerous Than They Appear (Or Advertised)?

Greg Webb — Fri, 25 Sep 2009 01:00:00 GMT

In its September 7^th article “What’s Really in Supplements?” The Wall Street Journal (WSJ)discusses the harmful side effects of a growing trend in the American dietary and strength conditioning communities: the taking of over-the-counter supplements.

Many supplements purport to aid in the building of muscle mass or in weight loss, claiming to do what prescription or illegal drugs do via an herbal means. However, the truth is that a great deal of these supplements contain at least trace amounts of the very drugs they claim to emulate.

Recent reports from the Food and Drug Administration (FDA) address the discovery of illegal performance-enhancing drugs in “allegedly natural supplements.” The WSJ article states that “[n]early two-thirds of American adults take dietary supplements, a broad category that includes vitamins, minerals and herbal products.” Supplement manufacturers are able to get their products quickly to market because they don’t require the extensive testing that new drugs do, and thus don’t require approval by the FDA. Furthermore, the WSJ says that “supplements that are made from products that were on the U.S. market before 1994 – as most commonplace ones are – can be sold without being reviewed by the FDA beforehand. Companies that include newer substances are supposed to inform the agency before they go on the market, but they don’t have to wait for approval.”

The recent attention stirred by the reports will be discussed during a hearing this month by a Senate Judiciary subcommittee. The focus of the hearing will be on dietary-supplement safety.

While officials at the Council for Responsible Nutrition are arguing that “no new laws are needed, citing new FDA manufacturing standards for supplements…as well as a requirement for supplement makers to tell the FDA when they get reports of serious side effects, which took effect at the end of 2007,” consumer advocates continue to call for closer monitoring.

A 2007 survey conducted by the British lab HFL Sport Science regarding supplements “found the undisclosed presence of steroids in at least trace amounts in 25% of the 52 samples analyzed,” and a 2008 article published in the journal Gastroenterology claimed that “9% of the 300 cases then recorded” could potentially be linked to supplement-taking. Since December 2008, “the FDA has issued warnings about more than 70 weight-loss supplements that included potentially dangerous ingredients.” The side effects of such ingredients could include seizure, heart attack and stroke. Liver and kidney failure have also been common in cases where a supplement taken regularly contained anabolic steroids. “Ed Wyszumiala, general manager of dietary supplement programs for NSF International, a nonprofit organization in Ann Arbor, MI that certifies supplements’ safety, says the drugs and steroids likely get into the products through a combination of deliberate spiking and inadvertent contamination.”

Vice President Andrew Shao of the Council for Responsible Nutrition “says safety problems are a ‘rare occurrence.’” He considers the HFL survey a “‘marketing tactic’” and says that consumers need to know what they’re taking as well. This is true. Consumers who take dietary supplements should be aware their ingredients and what those ingredients do. Research has been conducted on numerous herbs, most of which can be found online. In addition, Travis Tygart, chief executive of the U.S. Anti-Doping Agency, says that people who are interested in take supplements should speak with a physician. This would also help prevent dangerous interactions between prescription drugs and the supplements.

Preventative measures could include researching evidence, side effects and interactions at the National Library of Medicine (www.medlineplus.gov) under “Drugs and Supplements,” searching for specific supplements at www.fda.gov, as well as reading closely into what a supplement’s packaging discloses in subtext. “Certain suffixes in chemical names are common for steroids or tweaked versions of them. Among them are –one, -ene, -iol and –bol, though these can also appear in the names of legitimate ingredients. Some products also use versions of steroid names in their brands, like ‘tren’ to connote trenbolone.”

People using supplements should be aware of warning symptoms that could be indicative of an escalating problem. These include nausea, weakness or fatigue, fever, abdominal pain, chest pain, shortness of breath, yellow corneas and skin, and discolored urine, as cited by the FDA as warning signs of potential steroid use.

The Wall Street Journal article contains a complete list of resources for researching supplements.

Originally posted at InjuryBoard by Greg Webb

Homeopathic Drugs - "Remedies" - Potentially Hazardous?

Greg Webb — Mon, 29 Jun 2009 08:00:00 GMT

Although it was sold for many years as a drug for colds, Zicam Cold Remedy was never tested by federal regulators for safety like many other drugs. Because the drug is considered a “homeopathic remedy,” categorized as a highly diluted drug made from natural ingredients, they can legally be sold without any checks for safety, effectiveness, or even the right ingredients by the federal government. This was perfectly legal until consumers began losing their sense of smell.

Many scientists and health care professionals regard these homeopathic remedies as modern day snake oil, ineffective but mostly harmless because the substances in them are in such small amounts. They are similar to dietary supplements, which use many of the same natural ingredients and are also not tested for safety or benefit. The AP’s analysis of side-effect reports filed by the Food and Drug Administration (FDA), however, found more than eight hundred homeopathic ingredients were implicated in health problems last year; complaints ranged from vomiting to attempted suicide.

In the case of Zicam, the FDA tied the drug to 130 cases of consumers losing their sense of smell. Because of this, the agency asked Zicam manufacturer Matrixx Initiatives to stop marketing three products that contain zinc gluconate: Zicam Cold Remedy Nasal Gel, Nasal Swabs, and the discontinued Swabs in Kids' Size. In order for the drugs to be marketed again, the FDA requires they be tested for safety and benefit like other conventional drugs.

Are homeopathic remedies like Zicam effective? Many people swear by them, but is it essentially having a “placebo effect” on them? This writer is highly skeptical of these remedies, but, as long as they are essentially “harmless”, it is effectively just a situation of folks’ throwing away good money on these “remedies”. When the harm shifts from merely economic to real health problems, however, then a true harm to society may be occurring. The latter result may be indicative of a systemic problem requiring some form of intervention and oversight. Because of the number of issues that have arisen over the past decade or so with supplements and remedies, it seems as if we may be seeing a systemic problem, compounded by the greed of manufacturers producing and marketing these products.

Originally posted at InjuryBoard by Greg Webb

FDA Says Stop Using Popular Weight Loss Supplement Hydroxycut

Greg Webb — Fri, 01 May 2009 17:13:01 GMT

The U.S. Food and Drug Administration (FDA) says it has received 23 reports of serious liver injuries related to peoples' use of Hydroxycut products. Hydroxycut products are widely used dietary supplements for weight loss. The products are also used as "energy enhancers" and "fat burners".

The liver damage reports obtained by the FDA include problems ranging from jaundice to an injury so severe it required a liver transplant. There are also reports of seizures, cardiovascular disorders, and rhabdomy olysis (which can lead to kidney failure).

The recalled products include Hydroxycut Regular Rapid Release Caplets, Hydroxycut Carb Control and Hydroxycut Max Drink Packets. For more information on this recall, see the FDA website at www.fda.gov/bbs/topics/NEWS/2009/NEW02006.html

The products are manufactured by lovate Health Sciences in Ontario, Canada. The company is pulling 14 products, although the FDA says that not all of the products have been shown to be dangerous.

The products recalled contain a number of different ingredients, including herbal extracts. Dietary supplements do not require the same level of scrutiny before being sold to the public that pharmaceutical drugs require in the U.S.. Many consumer advocates have argued for years that there needs to be better governmental oversight of these industries. It seems that this latest incident is further evidence of the latter.

The FDA states that any people who have taken the recalled products should immediately see a physician if they have symptoms of nausea, vomiting, light-colored stools, excessive fatigue, weakness, stomach pain, itching, or loss of appetite, all of which may be indicators of a liver injury.

Originally posted at InjuryBoard by Greg Webb