The FDA and the Fukushima Fallout
April 1, 2011 · By Robert Alvarez
The FDA is disingenuous in its attempt to compare the radiation from a major nuclear accident to radiation exposures in everyday life.
“Radiation is all around us in our daily lives, and these findings are a miniscule amount compared to what people experience every day. For example, a person would be exposed to low levels of radiation on a round trip cross country flight, watching television, and even from construction materials,” said Patricia Hansen, an FDA senior scientist.
No matter how small the dose might be, it is disingenuous to compare an exposure to a specific radioisotope that is released by a major nuclear accident, with radiation exposures in every-day life. The FDA spokesperson should have informed the public that radioiodine provides a unique form of exposure in that it concentrates rapidly in dairy products and in the human thyroid. The dose received, based on official measurements, may be quite small, and pose an equally small risk. However, making a conclusion on the basis of one measurement is fragmentary at best and unscientific at worst. As the accident in Fukushima continues to unfold, the public should be provided with all measurements made of radioactive fallout from the Fukushima reactors to allow for independent analyses.
Moreover, the FDA has been asleep at the switch when it comes to protecting public health from medical radiation exposures. According to the National Council on Radiation Protection, radiation exposures to the American public from medical devices and source, which FDA regulates, has soared by nearly 600 percent since 1982. In 2002, the NCRP estimated that the public received an extra 53 millirem (0.53 mSv) per person per year from medical radiation sources.* In 2006, the NCRP estimates that this dose has jumped to 300 millirem(3mSv)--nearly three times the annual dose allowed by the U.S. EPA from nuclear facilities.
The single largest contributor responsible for half of this dose to the American public is from Computed Tomography or CT Scans, whose use has skyrocketed over the past several years. According to a study in the Archives of Internal Medicine, as many approximately 29,000 future cancers could be related to CT scans performed in 2007 alone.* FDA has yet to comment on how this may be affecting the health of the American public in every-day life.
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