Did Covid Shots Magnetize Humans?

Last week, I wrote about my 2015 experience with the mainstream media and my Australian debacle. I also set the story straight about the mudslinging and name-calling by the MSM that has continued since I spoke at the Ohio Health Committee in 2021. If you missed it, you can read it here.

This week, I’m addressing what I perceive to be the association (cause?) of why some people who had the jabs subsequently could place assorted metal objects on their body – which stuck – especially at the location of the jab. This substack was very time-consuming to write. I hope you’ll share it widely and become a free or paid member to support this work. Thank you in advance.

A package insert contains information written by the manufacturers to satisfy FDA standards and regulations. The 1966 Fair Packaging and Labeling Act required all consumer products to be honestly and informatively labeled. The law gave the FDA the ability to enforce these provisions on foods, drugs, cosmetics, and medical devices. Although patients may find the information about a drug or a vaccine useful, the intent of the FDA requirement is to educate physicians. The manufacturers have a legal requirement to provide physicians with information about the proper use and risks of the product so they can quickly and accurately educate the consumer/patient about the drug’s use and risks.

In 2006, the format of the prescribing information (PI) was amended to standardize the layout and ease of use. This was the first change since 1979, giving pharmacists and patients access to what was previously complex and complicated information. The information that is to be required on a package insert includes:

• Product name(s)

• Date of US approval

• Indications and usage

• Dosage and Administration

• Dosage forms and strengths

• Contraindications

• Warnings and precautions

• Listing of most common adverse reactions

• Drug Interactions

• Safety with pregnancy

• Black Box Warnings

• Recent Major Changes

• SECTION 11: Listing of all ingredients

• Clinical pharmacology

• Non-clinical toxicology: mutagenicity, teratogenicity, genotoxicity, carcinogenicity, infertility risks)

To learn more, and have this knowledge at your fingertips, I have a course on this subject called “How to Read a Package Insert” available at www.Learning4You.org

EUA

Emergency Use Authorization (EUA) permits the FDA to authorize the use of an unapproved medical product (drug, vaccine, or device) during a defined emergency that is considered to be a heightened risk to the public. Typically, when a new product is released, its use requires either informed consent or review and approval by an institutional review board. EUAs can waive both requirements for the duration of the ‘emergency.’  

The process for issuing an EUA is different than releasing an FDA-approved product. Under an EUA, the FDA authorizes the release of the unit based on a reasonable belief that the product ‘may be effective’ based on the best evidence available at the time. The covid jabs were released under the veil of the EUAand to this very day, none of the jabs used in the U.S. market have been FDA approved (Comirnaty and Spikevax were approved but not available in the US.)