WASHINGTON, D.C. – Today, America First Legal (AFL) launched a new investigation into the U.S. Food and Drug Administration (FDA) following a shocking discovery through litigation that revealed the FDA’s Division of General Endocrinology recommended the FDA approve puberty blockers for children despite direct knowledge that these drugs increase the risk of depression and suicidality.
Despite the trend in Europe to change course amidst a clear social contagion, the risks of transitioning children socially and medically, and the growing population of detransitioners, the Biden-Harris Administration is taking an approach diametrically opposed to the trends in Europe and shocking evidence in the United States.
To better understand the FDA’s activities with respect to the off-label use of puberty blockers in children, particularly as it relates to increased risk of suicide and depression, AFL has filed a Freedom of Information Act (FOIA) request with the FDA to obtain additional details surrounding this disturbing discovery.
Statement from Ian Prior, America First Legal Senior Advisor:
“While the rest of the civilized world is pulling back on the use of puberty blockers, cross-sex hormones, and medical castration of children, the Biden-Harris Administration has doubled down on this radical medical experimentation on children. The latest bombshell email from the FDA demonstrates a systemic and depraved rot in our federal government, and we will continue to investigate and expose it until it permanently ends,” said Ian Prior.
Read the FOIA here.
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