Thursday, September 2, 2021

Vexxine and Lousy Labeling

Frederick R Smith has moved to Frederick R. Smith Speaks (substack.com)

As detailed in Frederick R. Smith’s January 11, 2021 blog post “Twitter Tornadoes,” under the subheading of “The Delicious Sweet Dessert,” your author described writing a letter to his congressional representative to recommend new legislation. It inquired about the need to steer our nation to self-reliance for medical equipment and pharmaceuticals. His reply consisted of a two-page letter all about the wonderful work he had carried out with all those COVID bills passed creating more fiat currency. He simply sidetracked the request and had the gall to write this silly statement: “…be sure to avoid touching your eyes.” To be fair, it is probable he never saw the letter, and his staffers cut and paste a stock reply into a letter to make your author “happy.” Fred was nonplussed.

A follow up letter was drafted requesting an answer to the question. As expected, nothing came came back in response.    

Below is a new letter your author sent to his congressional representative concerning vaccine labeling. The use of “congressperson” is a bit tongue in cheek and feel free to copy and make use of it for your own needs. Stay tuned for the response from my good congressman (oops, congressperson). Based on the earlier interaction with this legislator, it promises to be quite entertaining.

The Letter

September 3, 2021

Dear Congressperson []

This letter addresses an obvious discontinuity in medical product labeling and warnings. Specifically, the lack of product information and warnings for vaccines and mRNA therapies.

As background, recently my ophthalmologist prescribed medicinal drops to treat high eye pressure (glaucoma). Upon opening the small box holding the eye drop bottle, I noticed a folded paper. This sheet, when unfolded, measures 7 by 22 inches. This paper, with exceedingly small lettering printed on both sides, holds extensive product data, warnings, and technical details. Researching online, I was able to download of copy of the pharmaceutical company’s PDF file with the same information. Please find enclosed a printed copy for your reference.

Throughout my life, I have taken many traditional vaccines with no hesitance. However, recently seeing the detailed product information about eye drops, and the absence of the same information for Covid-19 therapy shots (as well as other injectables), gave me pause for concern. Furthermore, television commercials for pharmaceuticals will always include a speedy narrative about side effects and precautions. Not so for the public service announcements or printed advertisements encouraging the Covid-19 shot.

It is astonishing that the pharmaceutical companies do not have to supply the same labeling for a traditional vaccine or “emergency use authorized” mRNA therapies as they do for eye drops. As you know, people who decide to take the Covid-19 injection see little if any information as compared to what we receive for eye drops (and other pharmaceuticals).

Given the above, I highly recommend the development of legislation to address this issue. The goal would be the promulgation of US Food and Drug Administration regulations that require the same level of consumer product information for traditional vaccines and mRNA therapies as detailed in the attached eye drop product safety and datasheet.

Thank your consideration and I look forward to your response.

Respectfully,

 /s/

Frederick R. Smith

Attachment: Cobian safety and datasheet

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