Dr. Kary Mullis Inventor of the PCR Test used for detection of Covid-19.

STORY-AT-A-GLANCE

The FDA can only grant emergency use authorization for a pandemic drug or vaccine if there’s no safe and effective preexisting treatment or alternative. Since there are several such alternatives, the FDA is legally required to revoke the emergency authorization for these shots.

While the COVID injections have been characterized as being somewhere around 95% effective against SARS-CoV-2 infection, this is the relative risk reduction, which tells you very little about its usefulness. The absolute risk reduction is only around 1% for all currently available COVID shots.

Antibody-dependent enhancement (ADE) refers to a condition where the vaccination augments your risk of serious infection. We are now starting to see evidence that ADE is occurring in the vaccinated population.

One of the most common side effects of the COVID shots is abnormal blood clotting, which can result in strokes and heart attacks.

Even microclots that don’t completely block the blood vessel can have serious ramifications. You can check for presence of microclots by performing a D-dimer blood test. If your D-dimer is elevated, you have clotting somewhere in your body.

STORY AT-A-GLANCE

> Data from Israel, where the vast majority of the population has been injected with the Pfizer mRNA concoction, show those “vaccinated” against COVID-19 and unvaccinated have the same infection rate, regardless of age. Empirical data from other countries also reveal the injections have no effect on transmission.

> Ivor Cummins suspects the obsession with COVID-19 injections has to do with profiteering and with justifying vaccine passports. The enormous emphasis on getting nearly everyone the COVID injection may also be related to elimination of the control group, which will effectively hide the real damage the injection is doing.

> Moderna and Pfizer have eliminated the original control groups by giving controls the real injection. This was done even though the trials are officially ongoing for another two years. So, there are no official control groups against which to assess the effectiveness and safety of these injections.

> Side effects of the COVID shots are vastly under-reported, so it’s very difficult to get a grasp on the real-world magnitude of the risks. According to a CDC whistleblower, the Vaccine Adverse Event Reporting System (VAERS) under-reports deaths by a factor of five or more.

> In sworn testimony, the whistleblower claims 45,000 Americans had died within three days of their COVID shots as of July 9, 2021. The numbers get even higher when looking at deaths occurring within a week or two of the injections.

“As the inventor of the messenger RNA (mRNA) vaccine platform, Dr. Robert Malone is one of the most qualified individuals to opine on the benefits and potential risks of this technology.”

STORY AT-A-GLANCE:

Safety data analysis and reporting in clinical trials of the COVID jabs appear to have been manipulated in at least some cases. One method for manipulating randomized clinical trial safety data is to only analyze the “per protocol” treatment group (those who completed all doses and were fully compliant with the study design) as opposed to “intent to treat” which would include all patients that have signed informed consent.

For example, if a participant only accepted one dose and trial protocol called for two, under a “per protocol” analysis, adverse events they experienced would be dismissed and not included in the safety analysis. This is a classic way to manipulate safety data in clinical research, and it’s usually forbidden.

Since the COVID shots only have emergency use authorization, they are experimental products and, as such, they are not authorized for marketing.

Bioethics are written into federal law. As an experimental trial participant, you have the right to receive full disclosure of any adverse event risks. Full disclosure of risks is not being done, and in fact is being suppressed.

Adverse event risks must also be communicated in a way that you can comprehend what the risks are, and the acceptance of an experimental product must be fully voluntary and uncoerced. Enticement is strictly forbidden.