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Family Friends Work Media Government Church

They’re starting to demand that I take the jab. The pressure is building. Everyone asks if I’ve taken the jab. Every day.

The ostracizing has started, too. It’s going to affect my livelihood.

I missed the part where all of these people were granted unrestricted access to my private medical care and records.

I’ve been telling them it’s none of their business - because it fucking isn’t - but, that’s not working anymore. They believe it is. It is for the “GREATER GOOD”, they say imperiously.

Reason and logic, legitimate concerns regarding an untested mRNA modifier, all over a disease that has an extraordinarily low morbidity rate…it all falls on deaf ears, lads.

It’s like Night of the Living Dead. They just keep coming.

Stay strong.

Family Friends Work Media Government Church They’re starting to demand that I take the jab. The pressure is building. Everyone asks if I’ve taken the jab. Every day. The ostracizing has started, too. It’s going to affect my livelihood. I missed the part where all of these people were granted unrestricted access to my private medical care and records. I’ve been telling them it’s none of their business - because it fucking isn’t - but, that’s not working anymore. They believe it is. It is for the “GREATER GOOD”, they say imperiously. Reason and logic, legitimate concerns regarding an untested mRNA modifier, all over a disease that has an extraordinarily low morbidity rate…it all falls on deaf ears, lads. It’s like Night of the Living Dead. They just keep coming. Stay strong.

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[–] [deleted] • 0 pt

When did this non FDA approved drug become a vaccine?

[–] • 0 pt

Non sequitur, the FDA approval is not required for a "drug"/product to qualify as vaccine

https://www.fda.gov/emergency-preparedness-and-response/coronavirus-disease-2019-covid-19/covid-19-vaccines

Coronavirus (COVID-19) Update

In mid-July, the FDA held a stakeholder call to discuss COVID-19 vaccines, including preliminary reports of Guillain-Barré Syndrome following Janssen (Johnson & Johnson) COVID-19 vaccination. Acting FDA Commissioner Janet Woodcock, M.D. and the Director of FDA's Center for Biologics Evaluation and Research, Peter Marks, M.D., Ph.D. were featured speakers. The call can be found on the FDA’s YouTube pageExternal Link Disclaimer.

COVID-19 Update 07/30/2021
Coronavirus (COVID-19) Update

On Wednesday, the FDA authorized an extension for the shelf life of the refrigerated Janssen (Johnson & Johnson) COVID-19 Vaccine, allowing the product to be stored at 2-8 degrees Celsius for six months.

COVID-19 Update 07/16/2021
Coronavirus (COVID-19) Update

The FDA formally accepts Priority Review designation for the Biologics License Application (BLA) for their mRNA vaccine to prevent COVID-19 in individuals 16 years of age and older.

[–] [deleted] • 0 pt

Changing the rules to further the agenda

[–] • 0 pt

They haven't changed the rules, the FDA's role isn't to tell whether a drug qualifies as a vaccine or not. Its role is to approve (or disapprove) it for medical prescription, that's all. You can have a european vaccine or drug for instance, that works, but which hasn't yet received the FDA's approval. As a result US medics can't prescribe it.

https://www.usa.gov/federal-agencies/food-and-drug-administration

Broadly speaking, the FDA "is responsible for protecting the public health by assuring the safety, efficacy, and security of human and veterinary drugs, biological products, medical devices, our nation's food supply, cosmetics, and products that emit radiation. The FDA also provides accurate, science-based health information to the public."

That's all, nothing more, nothing less