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Documents from U.S. Sen. Ron Johnson (R-WI), chairman of the Permanent Subcommittee on Investigations, have exposed evidence that appears to reveal the Biden administration chose to ignore a significant safety signal for ischemic stroke following administration of the Pfizer-BioNTech COVID-19 booster while it continued to advertise the shot to Americans as safe.
In a letter, dated March 23 and made public Wednesday, Johnson wrote to Department of Health and Human Services (HHS) Secretary Robert F. Kennedy, Jr., that, on August 31, 2022, the Biden Food and Drug Administration (FDA) authorized the mRNA Pfizer COVID-19 bivalent booster.
The senator noted as well that “[b]y late October 2022, HHS reported that approximately 14.4 million people 12 years and older had received the booster,” and then continued:
In November 2022, federal health officials became aware of a statistically significant safety signal for ischemic stroke among individuals age 65 and older following administration of the Pfizer-BioNTech COVID-19 bivalent booster. An ischemic stroke occurs when a blood vessel supplying the brain becomes blocked, preventing blood and oxygen from reaching parts of the brain. Despite the monthslong persistence of this safety signal in multiple vaccine safety surveillance systems, Biden’s FDA and Centers for Disease Control and Prevention (“CDC”) did not issue any formal health alerts, nor did they advise the public to avoid the vaccine. Instead, federal health officials continued to tell the public the vaccine was safe, but behind closed doors, they initiated multiple studies and statistical analyses—including a so-called “Stroke Project”—to investigate the validity of their assertion. These investigations continued through at least September 2025.
“I am sharing my preliminary findings to provide HHS and the public with even more evidence of the Biden administration’s unsupported and unyielding devotion to a harmful vaccine at the expense of the public’s health,” Johnson wrote to Kennedy. “The information and the records discussed below belong in the public domain, but as noted throughout this letter, the full extent of HHS’s awareness of the ischemic stroke safety signal remains incomplete and key records are still missing.”
According to a press release from Johnson’s office, the chairman released some 2,000 pages “of relevant HHS records available.”
“In addition to documents showing the detection of ischemic stroke following receipt of the Pfizer bivalent booster, the records released also contain internal communications between Biden health officials acknowledging significant statistical limitations in their ability to detect safety signals through their data analyses – called empirical Bayesian data mining.”
From very early on, prior to the COVID shot’s rollout, vaccine financier Bill Gates appeared to fumble in his response to questions about potential side effects from the mRNA shots. In addition, he assured Americans the FDA – as “the gold standard” federal health regulator – would “do a good job” in ensuring the vaccines did not produce “severe side effects.”
In July 2020, CBS News’ Norah O’Donnell asked Gates about the “concerning” finding during the Moderna COVID mRNA trials that “at least 80% of the participants experienced a systemic side effect” after the second dose, “ranging from severe chills to fevers.”
“So, are these vaccines safe?” O’Donnell asked.
“Well, the, uh, the FDA, not being pressured, will look hard at that – the FDA is the gold standard of regulators – and their current guidance on this, if they stick with that, is, is, very, very appropriate,” Gates said. “Uh, and, you know, the side effects were not super severe, that is, it didn’t cause permanent health problems for, uh, the things that they, you know, Moderna did have to go with a fairly high dose. And, so, uh, you know, to get the antibodies. Some of the other vaccines, uh, are able to go with lower doses to get, uh, responses that are, are pretty high, including the J&J and the Pfizer.”
“And, so, there’s a lot of characteristics of these vaccines, um, it’s great that we have multiple of them,” he said.
After O’Donnell interrupted Gates, repeating that “the data showed that everybody with a high dose had a side effect,” he responded, “Yeah, but some of that is, is not dramatic where you know it’s just, you know, super painful, but, yes, there we need to make sure there’s not severe side effects. The FDA, uh, I, I think will do a good job of that, uh, despite the pressure.”
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