FDA under fire for blocking documents on puberty blocker safety for kids

The US First Legal (AFL) on Friday sued the Food and Drug Administration, so that the biden-era records related to the internal guidance of the government for the recommended use of puberty for children for children could be obtained.

The Trump-Non-Knowing Legal Group had highlighted the communication through the pre-administration information Act (FOIA) request from the former administration, in which the FDA allegedly knew that these drugs had increased mental health risk, but still recommended to approve them for children.

Following those open communications, AFL requested documents with a separate Foia, which especially related to the internal guidance of the FDA for off-labeled use of these drugs. Despite accepting the federal information request, the FDA has not cooperated, and the time limit for production of documents is over.

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“Biden Administration pushed gender-deprived remedies on American children. Now, it is time to highlight what the authorities really knew,” AFL lawyer Will Scolinos said.

Similar to the current Foia request of AFL, it was necessary to engage in litigation to force the group to release the first set of documents.

However, finally, documents were issued to show the Biden-era division of General Endocrinology in the FDA that the agency recommended to approve puberty for children despite the knowledge that there were negative effects associated with them, such as an increase in depression, suicide and seizure risk.

“These drugs are definitely required to be approved for gender infection,” an FDA official of the agency’s endocrinology division said in an email. In the same communication, the FDA official also clearly stated that studies found that “the risk of depression and suicide increased, as well as the seizure risk increased.”

Such findings have also been confirmed by other studies.

Researchers at the University of Texas took a sample of 18 and older to 107,583 patients, who had gender dysphoria, some of which underwent gender surgery, and concluded that “gender-sensitive mental health aid … is” a “requirement to address post-surgical psychological risks.”

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The rate of depression was 25% compared to men without surgery to receive surgery, which was slightly from 12%. The anxiety rate between that group was 12.8% compared to 2.6%.

The same difference was also seen among women. People with surgery had 22.9% depression rate compared to 14.6% in non-surgical groups. Surgery women also had an anxiety rate of 10.5% compared to 7.1% for girls who did not perform surgery.

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Fox News reached the FDA for digital comment, but found no response immediately.

Fox News’ Melissa Rudy and Michael Doorgan contributed to this report