(should this be one of them there stickies?)
I don't have much of an FB following but I wrote a post that will hopefully make people curious about what's going on with the vax, and it's obfuscated enough that it isn't setting off community guidelines or fact check flags (yet). Feel free to use this.
Here's the post:
Long post, but please read. It'll just take a couple minutes, and it's really important.
So you know how those commercials for medicine usually end in that rapidfire list of possible side effects, usually a couple dozen of them rattled off within a few seconds?
Well, a bit over a year ago, an injectable medication was given temporary emergency authorization for public distribution, and subsequently, tens of thousands of companies (and many entire regions) have started requiring that their employees (or citizens (but not non-citizens... hmm)) partake in the consumption of the injectable medication.
Post-release, the manufacturer has collected data on side effects, effectiveness of the medication, and other useful information. This information was provided to the government agency that gave them the above authorization, and the manufacturer convinced the government to keep the data away from the public until 2076 (read: 55 years from now. When I'll be in my 80s.)
The public didn't like the concealment, so they're battling with the manufacturer and the government in the courts. They're winning. Data is starting to be released.
Of note, there's a document labeled "Cumulative analysis of post-authorization adverse event reports of [product] received through 28-FEB-2021". The information is from the first four months of authorization, and it has been on the market for 12 additional months since that cutoff. With no changes to the product, and an alleged permanent authorization of a "functionally identical" formulation of the medication. Pages 30 through 38 of this document are labeled "List of adverse events of special interest". And that's not, like, 4 items listed per page. That's 9 full pages of text, single-spaced, with ~1" margin and like 13pt font. It's a lot of text. And these are, based on that title, only the ones they're interested in. Oh, and the filename contains "postmarketing experience" so that's fun.
Some quick information about that list of adverse event reports:
The are one thousand, two hundred and ninety-one unique items. 1,291. Quantities of each listed item are not listed, but 1,291 unique conditions reported.
By a quick count, there are three thousand, three hundred and forty-six words contained in those entries. 3,346.
According to Guinness Book, the fastest talker can speak 655 words per minute when reading Hamlet. Normally I'd deduct points for Latin medical words, but I'll skip that because ye olde English can be a pain too. If he were to read the list of notable adverse events listed above, and then sped up to double speed like they do in the commercials, it would still be over two and a half minutes. A typical TV commercial is 30 seconds to a minute. That does not include any information about what this product does, where to get it, or who it's for - just the notable reported adverse events (that they tried to conceal from the public until 2076).
Granted this is the case with seemingly every medication, but the thing the product is supposed to prevent is listed as a reported adverse reaction of interest.
A quick skim of the list shows at least 40 different autoimmune conditions (33 of which start with the word "autoimmune", and Celiac is on the list too).
I'll give you one guess who the manufacturer is and what the product is. If I tell you, I'll get zuck'd. Paragraph #2 should be more than enough information to figure it out. Product name censored above to prevent zuckification as well, but this information is easy to locate now. Use Bing or DuckDuckGo or something, Google's scrubbing the info from their everything.
If this post stays up for any length of time, I'll throw the full list in a comment thread or something. You owe it to yourself to at least read this list, but you really should dig into this more.
I couldn't get the list of stuff into the comments without making 30 comments out of it, but it's the list from pg 30-38 of https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf
Drug approval submissions to FDA are contained in 5 Modules
This visual is from Module 5 Safety data. What I really want to see is Module 3 Drug Substance and Drug Product information. The mRNA coding for the Spike protein is the drug substance. The formulation is where the suspected graphene content resides, but formulation information has been completely hidden to this day and has not been disclosed in labeling as is required by law and regulation for purposes of obtaining informed consent of medication recipients.