Children's Health Defense
Despite public statements by government officials affirming the safety and efficacy of COVID-19 vaccines in early 2022, documents obtained by Children’s Health Defense (CHD) reveal that, at that time, public health officials were increasingly concerned about vaccine-related adverse events.
The 300 pages of documents released on Aug. 22 contain private correspondence from 2021 and early 2022 between U.S. Food and Drug Administration (FDA) and National Institutes of Health (NIH) officials, and emails from vaccine-injured individuals to NIH scientists.
CHD requested the documents via a Freedom of Information Act (FOIA) request in 2022. In April 2023, CHD sued the NIH to obtain the records after the agency failed to respond. In an October 2023 settlement, the NIH agreed to produce 7,500 pages of documents at a rate of 300 pages per month.
Last month’s tranche of documents showed that in late 2021 and early 2022, FDA and NIH officials privately expressed concerns about the growing rate of adverse events related to the COVID-19 vaccines — concerns that reached high-level FDA officials.
A Jan. 24, 2022, email (pages 239-240) to Dr. Janet Woodcock, the FDA’s principal deputy commissioner of food and drugs, and Peter Marks, M.D., Ph.D., director of the FDA’s Center for Biologics Evaluation and Research, alerted them to the existence of “scientific data” regarding adverse events…
READ FULL ARTICLE HERE… (childrenshealthdefense.org)
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