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A new batch of documents [ [link removed] ] obtained by Judicial Watch under a recent Freedom of Information Act Request (FOIA) raises more questions about the secret dealings of the U.S. government, namely . . . why do the UK and U.S. have a confidentiality agreement related to Pfizer’s COVID-19 vaccine and adverse events — what does it say and why didn’t the American people know about it?
In a Dec. 9, 2020 email exchange [ [link removed] ], Philip Krause, a former member of the FDA’s vaccine advisory committee who resigned in 2022 when the Biden administration pushed its COVID-19 booster shot plan, sent the following email to officials with the UK’s Medicines and Healthcare products Regulatory Agency (MHRA). Copied on the email was Dr. Marion Gruber, who later resigned with him.
In the email, Krause asks if it is possible to talk under “our confidentiality agreement.”
There was an FDA vaccine advisory meeting scheduled for Dec. 10, 2020, and Krause was seeking information on anaphylactoid reactions to the Pfizer-BioNTech vaccine reported in the UK. The MHRA’s Jonathan Mogford provides information on “two cases of anaphylactoid reactions in individuals with a strong past history of allergic reactions.”
Dr. Peter Marks, director of the Center for Biologics Evaluation and Research within the U.S. Food and Drug Administration (FDA), references this “mutual confidentiality agreement” with the MHRA in an email stating, “it would be very helpful if our Office of Vaccines could receive additional details on [redacted] from MHRA under the terms of our mutual confidentiality agreement.”
Mogford replies, “… attached are [redacted] hope that’s helpful in the meantime. If I can just remind – information shared under our confidentiality agreement.”
Mogford did not provide a copy of the confidentiality agreement, and the FDA did not respond to questions about the agreement either.
Jamie Convisser with the MRHA responds to Krause and says information shared is not in the public domain, obviously reinforcing that it needed to be kept on the low. What would happen if people on the receiving end of COVID vaccine propaganda found out the shot could cause injuries?
Other emails obtained by Judicial Watch appear to be heavily redacted and relate to the administration of COVID-19 vaccines with other vaccines during pregnancy.
The emails were obtained [ [link removed] ] after the nonprofit sued the Department of Health and Human Services for failing to respond to an Aug. 30, 2021, FOIA request for:
All emails sent to and from members of the Vaccines and Related Biological Products Advisory Committee regarding adverse events, deaths and/or injuries caused by investigatory vaccines for the prevention or treatment of SARS-CoV-2 and/or COVID-19 currently produced by Pfizer/BioNTech, Moderna and/or Johnson & Johnson.
“It again took a lawsuit for the Biden administration to hand over, albeit heavily redacted, information regarding the safety of the COVID vaccines that the public has every right to know,” Judicial Watch President Tom Fitton said in a statement. “This disturbing batch of new documents have uncovered a secret confidentiality agreement tied to COVID vaccine safety issues and emails that raise new questions about the vaccines and pregnancy.”
In a press release [ [link removed] ] on its website, Judicial Watch said it is pursuing challenges against the agency’s redactions under FOIA. In a previous FOIA lawsuit, Judicial Watch received 1,081 pages [ [link removed] ] of records from HHS involving internal discussions about myocarditis and COVID-19 vaccines and “adverse events for which a contributory effect of the vaccine could not be excluded.” 
It’s sad that organizations like Judicial Watch have to continuously file lawsuits to obtain information U.S. regulatory agencies by law are required to turn over and are failing to do so in an effort to cover up COVID-19 vaccine safety issues.
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