How The FDA Did Nothing to Verify the Long Term Safety Of The Covid Vaccines

ByShaun Snapp

Last Updated on August 17, 2022 by Shaun Snapp

Executive Summary

  • The FDA did not lift a finger to check the long term safety of the covid vaccines.
  • The public is completely unaware of this fact.

Introduction

The FDA has not followed up on the safety of the covid vaccines. They have also not addressed the high percentage of adverse effects from the VAERS database that is maintained by CDC or the adverse reaction database that the WHO maintains. The FDA’s own adverse reaction database is little discussed.

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Not Following Up on Long Term Side Effects

Something that is little known is the short period of time for which adverse effects are tracked. This is particularly true as of the covid vaccines as they cause all manner of long-term problems.

This is explained in the following quotation.

…patients were only followed prospectively for approximately 7 days after immunization for “solicited” adverse events, and then relied on “unsolicited” reports of adverse events
for approximately 30-60 days after immunization. Serious noninfectious events occurring after this 30-60 day period were not part of the published data. patients were only followed prospectively for approximately 7 days after immunization for “solicited” adverse events, and then relied on “unsolicited” reports of adverse events for approximately 30-60 days after immunization. Serious noninfectious events occurring after this 30-60 day period were not part of the published data. Given that some of the vaccine clinical trials recruited patients in the third world, patients with low education, and potentially even elderly with dementia the patients can not be expected to understand when they may be having an serious event that needs reporting or how
to report it. For these and others reason only 5% of adverse events are generally ever reported [8]. – US COVID-19 Vaccines Proven to Cause More Harm than Good Based on Pivotal Clinical Trial Data Analyzed Using the Proper Scientific Endpoint, “All Cause Severe Morbidity”

These types of segments are where the establishment media, which receives large payments from pharmaceutical companies, covers FDA press releases that obscure the truth. The FDA puts far more effort into communicating sugar-coated information about how “safe” the vaccines are to the appropriate compliant media outlets than verifying vaccine safety. 

In addition to online databases, safety issues with vaccines have come in from whistleblowers around the world. And the FDA has nothing to say about this. As is stated in the video, the objective is to sweep the adverse reactions under the rug.

Conclusion

The FDA could not be bothered to keep tabs on the safety of the covid vaccines even though they approved these vaccines after only two months of study, which is a very unusually short duration. They did nothing and did not seem to want to know about adverse effects illustrates how much the FDA is now entirely captured by pharmaceutical interests. As is explained in the article, The FDA, CDC, and NIH Do Not Want Adverse Drug Reactions Counted. The FDA has no interest in adverse reactions being communicated to the public.