All Vaccines Are Experimental (Part I)

All Vaccines Are Experimental (Part I)

Vaccine regulatory approvals are supported by:

  • Fake placebos (so-called “placebos” that contain neurotoxins),
  • Fake controls (so-called “controls” of people who are also vaccinated),
  • Short-term testing windows (so-called “tests” with monitoring periods as short as 3-days), and
  • Long-term passive surveillance of vaccine injuries (so-called “surveillance” with an unknown to approximately 99% failure rate of reporting).

In this manner, vaccine science has not even evolved enough to recognize the basic dictionary definition of words, let alone become advanced enough to reach the status of “settled science”.


FDA (2018). Common Ingredients in U.S. Licensed Vaccines. https://www.fda.gov/vaccines-blood-biologics/safety-availability-biologics/common-ingredients-us-licensed-vaccines

ATSDR (2011). Substances A-Z. Toxic substances portal. https://www.atsdr.cdc.gov/substances/indexAZ.asp

FDA (2020). Vaccines Licensed For Use In the United States. https://www.fda.gov/vaccines-blood-biologics/

CDC (2017). Chapter 21: Surveillance for Adverse Events Following Immunization Using the Vaccine Adverse Event Reporting System. CDC: Manual for the Surveillance of Vaccine-Preventable Diseases. https://www.cdc.gov/vaccines/pubs/surv-manual/chpt21-surv-adverse-events.html

Lazarus, R., et al. (2007). Grant Final Report: Electronic Support for Public Health–Vaccine Adverse Event Reporting System (ESP:VAERS). The Agency for Healthcare Research and Quality (AHRQ) U.S. Department of Health and Human Services. https://healthit.ahrq.gov/sites/default/les/docs/publication/r18hs017045-lazarus-nal-report-2011.pdf

FDA (2006). Guidance Document: Adverse Reactions Section of Labeling for Human Prescription Drug and Biological Products — Content and Format. https://www.fda.gov/media/72139/download

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