Wall Street Journal Just Discovered Vaccine Injuries!

Officials Neglect Covid Vaccines’ Side Effects

Peter Hotez Exposed as Tool/Fraud/Psychopath

Pfizer’s Rap Sheet

Pfizer Has a Long History of Fraud, Corruption and Using Children as Human Guinea Pigs

Pfizer/FDA Vaccine Cover-Up Exposed: Adverse Reactions

FIRST SENTENCE:

“The information contained in this document is proprietary and confidential.”

9 pages of adverse reactions at the end of the file. I believe this is the report, PDF.

Pfizer & FDA attempted to cover this up for 75 years (not a joke), but a judge ordered its release.

CDC Vax Debacle: Unscientific Time Schedule to Rush Out Vaccines

THIS is why you don’t allow the government to force drugs into you.

#InformedMedicalConsent

#MedicalConsent

#Vaccines

What happened to first do no harm?

Pfizer Whistleblower & Cover-Up

Jimmy Dore has set up shop on RUMBLE, which seems like a good idea.

Vaccine Mismanagement Threatens America

Trump and Biden are pushing to vaccinate with one shot instead of the two that are necessary and reserves are depleted.

#ANTISCIENCE
#BADMEDICINE
#PANDEMIC

Corruption has destroyed regulatory oversight (for VACCINES)

“They do not measure the difference between infection and noninfection as a primary motivation.”

Covid-19 Vaccine Protocols Reveal That Trials Are Designed To Succeed

“Vaccine efficacy is typically proved by large clinical trials over several

years. The pharmaceutical companies intend to do trials ranging from thirty thousand to sixty thousand participants. This scale of study would be sufficient for testing vaccine efficacy. The first surprise found upon a closer reading of the protocols reveals that each study intends to complete interim and primary analyses that at most include 164 participants. “

“For Moderna, the initial interim analysis will be based on the results of infection of only 53 people. “

“Johnson & Johnson is the only trial that requires the inclusion of severe Covid-19 cases, at least 5 for the 75 participant interim analysis.”

FDA COVER-UP: ROUNDUP IN YOUR FOOD

 

 

But the internal documents obtained by the Guardian show the FDA has had trouble finding any food that does not carry traces of the pesticide.

Weedkiller found in granola and crackers, internal FDA emails show

The Food and Drug Administration (FDA) has been testing food samples for residues of glyphosate, the active ingredient in hundreds of widely used herbicide products, for two years, but has not yet released any official results.

FDA to Test for Glyphosate

 

 

You mean they haven’t been all this time?

Heads should roll. Prosecutions for corruption, negligence and malfeasance should go forward.

FDA to Start Testing for Glyphosate in Food

The U.S. Food and Drug Administration (FDA), the nation’s chief food safety regulator, plans to start testing certain foods for residues of the world’s most widely used weed killer after the World Health Organization’s cancer experts last year declared the chemical a probable human carcinogen.

The FDA’s move comes amid growing public concern about the safety of the herbicide known as glyphosate, and comes after the U.S Government Accountability Office (GAO)rebuked the agency for failing to do such assessments and for not disclosing that short-coming to the public.

Private companies, academics, and consumer groups have recently launched their own testing and claim to have detected glyphosate residues in breast milk, honey, cereal, wheat flour, soy sauce, infant formula, and other substances.

 

New England Journal of Medicine Blows Whistle on GMOs!

GMOs, Herbicides, and Public Health

Monsanto’s lies and its troll army are contradicted in no uncertain terms. They have monkeyed with science in numerous ways, and corrupted the process of ensuring food safety.

In our view, the science and the risk assessment supporting the Enlist Duo decision are flawed. The science consisted solely of toxicologic studies commissioned by the herbicide manufacturers in the 1980s and 1990s and never published, not an uncommon practice in U.S. pesticide regulation. These studies predated current knowledge of low-dose, endocrine-mediated, and epigenetic effects and were not designed to detect them. The risk assessment gave little consideration to potential health effects in infants and children, thus contravening federal pesticide law. It failed to consider ecologic impact, such as effects on the monarch butterfly and other pollinators. It considered only pure glyphosate, despite studies showing that formulated glyphosate that contains surfactants and adjuvants is more toxic than the pure compound.

…This decision was made in haste. It was based on poorly designed and outdated studies and on an incomplete assessment of human exposure and environmental effects.

…National Toxicology Program should urgently assess the toxicology of pure glyphosate, formulated glyphosate, and mixtures of glyphosate and other herbicides.

…Labeling will deliver multiple benefits. It is essential for tracking emergence of novel food allergies and assessing effects of chemical herbicides applied to GM crops.

Frankenfish Alert

Frankenfish Flops Risk Assessment

…AquAdvantage Salmon reveals that Canadian government scientists found significant problems with the fish, including increased susceptibility to disease and widely inconsistent growth rates. As a result of this newly released draft risk assessment, U.S. NGOs are calling for the U.S. FDA to stop its own review of the fish.