Judicial Watch says it wants to know why the Biden administration is hiding information about the safety of Covid vaccines– vaccines the government has aggressively promoted and even mandated.
Public health agencies continually state that the Covid vaccines are safe and effective, yet the agencies and vaccine makers have not released important information that would substantiate the claims. In fact, most of the data that’s been made public is the result of Freedom of Information Act (FOIA) lawsuits by watchdog groups, non-profit organizations, and independent scientists.
Judicial Watch has filed a new lawsuit for information after the National Institutes of Allergies and Infectious Diseases (a component of HHS) inadequately responded to a June 1, 2022, FOIA request for the following:
- All safety studies, data, reports, and analyses produced by the Division of Microbiology and Infectious Diseases (DMID) relating to the safety of ‘vaccines’ and/or gene therapies to treat and/or prevent SARS-CoV-2 and/or Covid-19 made by Pfizer, BioNTech, Moderna, Johnson & Johnson, and Janssen.
- All emails sent to and from the following DMID officials relating to the safety of ‘vaccines’ and/or gene therapies to treat and/or prevent SARSCoV-2 and/or Covid-19 made by Pfizer, BioNTech, Moderna, Johnson & Johnson, and Janssen:
a. The Director of DMID
b. The head of the Office of Genomics & Advanced Technologies
c. The head of the Office of International Research in Infectious Diseases
d. The head of the Office of Regulatory Affairs
e. The head of the Office of Clinical Research Affairs
f. The head of the Clinical Trials Management Section
g. The head of the Virology Branch
h. The head of the Respiratory Diseases Branch
i. The head of the Influenza, SARS, and Other Viral Respiratory Diseases Section
On May 3, 2022, the National Institutes of Health (NIH) released a paper titled “Safety and Immunogenicity of a Third Dose of SARS-CoV-2 mRNA Vaccine – An Interim Analysis” that “evaluated early safety and immunogenicity after a third mRNA vaccination in adults who received the mRNA-1273 primary series in the Phase 1 trial approximately 9 to 10 months earlier.”
Contributors to that study include three affiliates of the DMID: Mamodikoe Makhene (DMID medical officer), Wendy Buchanan (DMID Clinical Project Manager) and Paul Roberts (DMID Chief Respiratory Pathogens Clinical Research).
Judicial Watch accuses the Biden administration is playing shell games with documents on Covid vaccines saying that the administration’s inadequate response and inability to produce the requested vaccine safety documents further undermines public confidence in these already highly controversial drugs.
Read full case at this link: (Judicial Watch, Inc. v. U.S. Department of Health and Human Services (No. 1:22-cv-03153)).
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