Food Drug Administration (FDA) remains diligent to protect soy industry profits while they overwhelmingly acknowledge that toxic components of soybeans include; estrogenic endocrine disruptors, inhibitors of several essential developmental enzymes, phytic acid, and heavy metals, that are each and all capable of causing severe and irreversible physiological, reproductive, and neurological adverse effects especially during most vulnerable developmental (fetus, infant, child) exposure.
FDA Commissioner Hamburg’s assistant Michael Taylor had been an attorney for Monsanto prior to his FDA position. Monsanto profits in the billions from the marketing of soybean seed.
Food and Drug Administration remains diligent to protect soy industry profits while simply ignoring complete duty to maintain the best health and well-being of America’s children
“It is urgently necessary that Congress take immediate action to investigate and demand that the FDA lawfully post appropriate soy phyto-toxic WARNING labels for public disclosure to protect the health of children from a number of adverse effects.
Also of importance is the 2010 NTP Brief on soy infant formula of which concludes “Clear evidence of (soy formula) adverse effects” to absolutely warrant WITHDRAWAL of soy formulas from the U.S. marketplace as equal to the vast majority of countries around the world. The first 3 ingredients of soy infant formulas are; Corn syrup, soy and sugar, of which each and all are FDA known as developmental poisons.”
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