US Agencies Quietly Studying Reports of Post-Vaccination Neurological Issues

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Two U.S. agencies have been quietly studying neurological problems that have appeared in people who have had COVID-19 vaccines, The Epoch Times has found.

The Food and Drug Administration (FDA) and National Institutes of Health (NIH) have been conducting separate research projects into post-vaccination neurological issues, which have manifested with symptoms like facial paralysis and brain fog and have been linked in some cases with the vaccines, according to emails reviewed by The Epoch Times.

One attempt to gain understanding of a problem that experts around the world are struggling to understand is being carried out by Dr. Janet Woodcock, who was acting commissioner of the FDA until Feb. 17.

Woodcock, now the FDA’s principal deputy director, has been personally evaluating neurologic side effects from the COVID-19 vaccines since at least Sept. 13, 2021, according to the emails, many of which have not been reported on previously. FDA epidemiologists are also gathering data to look into the issues, according to messages from Dr. Peter Marks, another top FDA official.

A team at the NIH’s National Institute of Neurological Disorders and Stroke (NINDS), meanwhile, started seeing patients reporting vaccine injuries for a study in early 2021 after receiving complaints shortly after the vaccines were made available. A portion of the patients was examined in person at the Bethesda, Maryland, facility.

None of the reviews or studies appear to have been announced, and health officials have said little about them publicly, despite a growing recognition among experts that at least some issues are likely linked to the vaccines.

FDA

Woodcock was aware of reports of post-vaccination issues by April 16, 2021, according to the emails.

Woodcock said she was sorry for the ordeals people were going through and that she was trying to find ways to examine what was happening. Eventually, she disclosed that she was working on an evaluation of “neurologic side effects from the COVID 19 vaccines,” according to a Sept. 16, 2021, email reviewed by The Epoch Times.

Prodded by people with diagnosed vaccine injuries, Woodcock insisted she was still working on the project.

“I am awaiting some information from the epidemiologists that I expect to get tomorrow,” she wrote on Nov. 16, 2021. “We are having difficulty pinning down these nervous system-related events that have been brought to our attention. I’ve asked for specific searches of the reports we get both from here and ex-U.S. (as these vaccines have been used in many countries) as well as from trials, where oversight of participants is greater.”

Woodcock said she was aware that people who suffer issues after getting vaccinated were looking for guidance on treatment but that there was “not a lot of certainty about what causes the symptoms.”

Woodcock confirmed to The Epoch Times in an email that the evaluation is still ongoing and has not been completed.

“When we know something definitive, we will put out a statement if warranted,” she said.

The FDA regulates vaccines, medical devices, and cosmetics, in addition to other products.

Marks, who heads the FDA’s center in charge of regulating vaccines, wrote in one email in November 2021 that epidemiologists at the FDA are “looking into this.”

“I work closely with them, and know that they are very committed to understanding whatever adverse events might be attributable to the vaccines that we regulate,” he added.

Marks has met with patients reporting vaccine injuries on multiple occasions, according to emails reviewed by The Epoch Times. He has been alerted to both cases and studies regarding potential vaccine injuries. He often writes that the FDA will work through the papers and keep following up.

“We will continue to carefully evaluate all serious reports of adverse events following COVID-19 vaccination and are committed to transparency about any findings,” he said in one missive.

Marks declined to answer questions, forwarding them to FDA spokespersons.

A spokesperson told The Epoch Times in an email that the systems in place to monitor the safety of COVID-19 vaccines have identified several issues “potentially associated with vaccination,” including the neurological disorder known as Guillain-Barré syndrome, the combination of blood clotting and low blood platelet levels known as thrombosis with thrombocytopenia syndrome (TTS), and several forms of heart inflammation, including myocarditis.

“The chance of having these events occur is very low,” the spokesperson said. “To date, the systems for monitoring COVID-19 vaccine safety have not identified additional safety signals for serious neurological outcomes following COVID-19 vaccination.”

FDA epidemiologists and experts at the Centers for Disease Control and Prevention (CDC) continuously analyze data from the passive reporting system known as the Vaccine Adverse Event Reporting System (VAERS) to identify potential signals that would suggest a need for more in-depth study and consult with NIH experts about the analyses, according to the FDA. Reports to VAERS have spiked since the COVID-19 vaccines became available, and some patients who filed VAERS reports told The Epoch Times that nobody followed up with them.

Source: The Epochtimes

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