Chelation therapy was approved in 1991 as an effective method of treating lead and other heavy metal poisoning. During the process, a synthetic solution called EDTA – ethylenediaminetetraacetic acid – is injected into the body and attaches itself to the heavy metal molecules, allowing them to pass through the body without being absorbed any further.
Doctors and health officials warn consumers that chelation therapy, while effective, carries significant health risks. The treatment should only be administrated by a professional while the patient is under medical supervision.
Recently, the Food and Drug Administration (FDA) warned customers not to purchase Thorne Research’s Captomer or Captomer-250, marketed as an over the counter form of chelation therapy. The company voluntarily recalled the drug after “several adverse health events” were reported.
The active ingredient in the product is meso-2, 3-dimercaptosuccinic acid (DMSA), and it is currently available in a prescription product used to treat lead poisoning in children. Despite that fact, the government agency maintains that there is no FDA-approved OTC version of chelation therapy.
Due to the health risks involved, the FDA recommends that customers seek professional care for any type of heavy metal poisoning, and avoid any OTC product promising chelation-like results.
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Drug companies are not above presenting a half-truth to conceal a lie. They will market drugs that have never been approved by the FDA, or never approved outside of a specific use. Their main goals are high sales and profits, often at the risk of public health.
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[Did You Know: More than 30 chelation-related deaths have been reported since the 1970s, including several children.]
Proffitt & Cox, LLP – Columbia Injury Lawyer