I didn’t mean for this website to go as basic as this, quite the opposite, but apparently there’s still a huge need for basic stuff for basic people.
And we can’t really advance much without covering the basics properly.

Study: Pfizer, GSK, Eli Lilly Topped Military Industry in Defrauding US Govt (2010)

Here’s an older meme that’s basically a sequel to the one above

Based on this testimony:

Now compare my memes against this Pfizer press release: Pfizer and BioNTech Confirm High Efficacy and No Serious Safety Concerns Through Up to Six Months Following Second Dose in Updated Topline Analysis of Landmark COVID-19 Vaccine Study

Not much else to add, besides our motto: “Don’t believe what we say, research what we say!”

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ORDER

I so wanted to start the year with some good news rather than more gloom and doom, like most of the data on my hard disks… And we’re damn lucky!

So yeah, Aaron Siri has just announced he won another case against the FDA, the judge correcting the previous abomination about the Pfizer data release. This is the announcement from his Substack:

INSTEAD OF FDA’S REQUESTED 500 PAGES PER MONTH, COURT ORDERS FDA TO PRODUCE PFIZER COVID-19 DATA AT RATE OF 55,000 PAGES PER MONTH!

A great win for transparency that removes a stranglehold “health” authorities have had on data independent scientists need to offer solutions and address serious issues with the vaccine program.

Aaron Siri1 hr ago267110

On behalf of a client, my firm requested that the FDA produce all the data submitted by Pfizer to license its Covid-19 vaccine.  The FDA asked the Court for permission to only be required to produce at a rate of 500 pages per month, which would have taken over 75 years to produce all the documents. 

I am pleased to report that a federal judge soundly rejected the FDA’s request and ordered the FDA to produce all the data at a clip of 55,000 pages per month!

This is a great win for transparency and removes one of the strangleholds federal “health” authorities have had on the data needed for independent scientists to offer solutions and address serious issues with the current vaccine program – issues which include waning immunity, variants evading vaccine immunity, and, as the CDC has confirmed, that the vaccines do not prevent transmission.

No person should ever be coerced to engage in an unwanted medical procedure.  And while it is bad enough the government violated this basic liberty right by mandating the Covid-19 vaccine, the government also wanted to hide the data by waiting to fully produce what it relied upon to license this product until almost every American alive today is dead.  That form of governance is destructive to liberty and antithetical to the openness required in a democratic society. 

In ordering the release of the documents in a timely manner, the Judge recognized that the release of this data is of paramount public importance and should be one of the FDA’s highest priorities.  He then aptly quoted James Madison as saying a “popular Government, without popular information, or the means of acquiring it, is but a Prologue to a Farce or a Tragedy” and John F. Kennedy as explaining that a “nation that is afraid to let its people judge the truth and falsehood in an open market is a nation that is afraid of its people.” 

The following is the full text of the Judge’s order, a copy of which is also available here.

UNITED STATES DISTRICT COURT

PHMPT, Plaintiff v. FDA, Defendant, No. 4:21-cv-1058-P

ORDER

This case involves the Freedom of Information Act (“FOIA”). Specifically, at issue is Plaintiff’s FOIA request seeking “[a]ll data and information for the Pfizer Vaccine enumerated in 21 C.F.R. § 601.51(e) with the exception of publicly available reports on the Vaccine Adverse Events Reporting System” from the Food and Drug Administration (“FDA”). See ECF No. 1. As has become standard, the Parties failed to agree to a mutually acceptable production schedule; instead, they submitted dueling production schedules for this Court’s consideration. Accordingly, the Court held a conference with the Parties to determine an appropriate production schedule.[1] See ECF Nos. 21, 34.

“Open government is fundamentally an American issue” – it is neither a Republican nor a Democrat issue.[2] As James Madison wrote, “[a] popular Government, without popular information, or the means of acquiring it, is but a Prologue to a Farce or a Tragedy; or, perhaps, both. Knowledge will forever govern ignorance: And a people who mean to be their own Governors, must arm themselves with the power which knowledge gives.”[3] John F. Kennedy likewise recognized that “a nation that is afraid to let its people judge the truth and falsehood in an open market is a nation that is afraid of its people.”[4] And, particularly appropriate in this case, John McCain (correctly) noted that “[e]xcessive administrative secrecy . . . feeds conspiracy theories and reduces the public’s confidence in the government.”[5]

Echoing these sentiments, “[t]he basic purpose of FOIA is to ensure an informed citizenry, [which is] vital to the functioning of a democratic society.” NLRB v. Robbins Tire & Rubber Co., 437 U.S. 214, 242 (1977). “FOIA was [therefore] enacted to ‘pierce the veil of administrative secrecy and to open agency action to the light of public scrutiny.’” Batton v. Evers, 598 F.3d 169, 175 (5th Cir. 2010) (quoting Dep’t of the Air Force v. Rose, 425 U.S. 352, 361 (1976)). And “Congress has long recognized that ‘information is often useful only if it is timely’ and that, therefore ‘excessive delay by the agency in its response is often tantamount to denial.’” Open Soc’y Just. Initiative v. CIA, 399 F. Supp. 3d 161, 165 (S.D.N.Y. 2019) (quoting H.R. REP. NO. 93-876, at 6271 (1974)). When needed, a court “may use its equitable powers to require an agency to process documents according to a court-imposed timeline.” Clemente v. FBI, 71 F. Supp. 3d 262, 269 (D.D.C. 2014).

Here, the Court recognizes the “unduly burdensome” challenges that this FOIA request may present to the FDA. See generally ECF Nos. 23, 30, 34. But, as expressed at the scheduling conference, there may not be a “more important issue at the Food and Drug Administration . . . than the pandemic, the Pfizer vaccine, getting every American vaccinated, [and] making sure that the American public is assured that this was not [] rush[ed] on behalf of the United States . . . .” ECF No. 34 at 46. Accordingly, the Court concludes that this FOIA request is of paramount public importance.

“[S]tale information is of little value.” Payne Enters., Inc. v. United States, 837 F.2d 486, 494 (D.C. Cir. 1988). The Court, agreeing with this truism, therefore concludes that the expeditious completion of Plaintiff’s request is not only practicable, but necessary. See Bloomberg, L.P. v. FDA, 500 F. Supp. 2d 371, 378 (S.D.N.Y. Aug. 15, 2007) (“[I]t is the compelling need for such public understanding that drives the urgency of the request.”). To that end, the Court further concludes that the production rate, as detailed below, appropriately balances the need for unprecedented urgency in processing this request with the FDA’s concerns regarding the burdens of production. See Halpern v. FBI, 181 F.3d 279, 284–85 (2nd Cir. 1991) (“[FOIA] emphasizes a preference for the fullest possible agency disclosure of such information consistent with a responsible balancing of competing concerns . . . .”).

Accordingly, having considered the Parties’ arguments, filings in support, and the applicable law, the Court ORDERS that:

1. The FDA shall produce the “more than 12,000 pages” articulated in its own proposal, see ECF No. 29 at 24, on or before January 31, 2022.

2. The FDA shall produce the remaining documents at a rate of 55,000 pages every 30 days, with the first production being due on or before March 1, 2022, until production is complete.

3. To the extent the FDA asserts any privilege, exemption, or exclusion as to any responsive record or portion thereof, FDA shall, concurrent with each production required by this Order, produce a redacted version of the record, redacting only those portions as to which privilege, exemption, or exclusion is asserted.

4. The Parties shall submit a Joint Status Report detailing the progress of the rolling production by April 1, 2022, and every 90 days thereafter.[6]

SO ORDERED on this 6th day of January, 2022.


[1] Surprisingly, the FDA did not send an agency representative to the scheduling conference.

[2] 151 CONG. REC. S1521 (daily ed. Feb. 16, 2005) (statement of Sen. John Cornyn).

[3] Letter from James Madison to W.T. Barry (August 4, 1822), in 9 WRITINGS OF JAMES MADISON 103 (S. Hunt ed., 1910).

[4] John F. Kennedy, Remarks on the 20th Anniversary of the Voice of America (Feb. 26, 1962).

[5] America After 9/11: Freedom Preserved or Freedom Lost?: Hearing Before the S. Comm. on the Judiciary, 108th Cong. 302 (2003).

[6] Although the Court does not decide whether the FDA correctly denied Plaintiff’s request for expedited processing, the issue is not moot. Should the Parties seek to file motions for summary judgment, the Court will take up the issue then.

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Right off the bat:

SOURCE: FDA
  1. You can’t have a single product with two commercial names in the same place, at the same time. BionTech hasn’t been erased. So there are two Pfizer products: Comirnaty and Pfizer-BionTech.
  2. Until the vial content is independently audited, we can’t know the difference between the two, because this info has been redacted from the publicly available letters.
    But we know for sure there is one and it’s significant enough to earn a new commercial name.
  3. (After four updates that I had to erase to clarify and make this more readable)

    “BioNTech said it was developing four vaccine candidates under a programme named BNT162 with its partner, pharma giant Pfizer… BioNTech, which awarded the rights in China to BNT162 to Shanghai Fosun Pharmaceutical under a March collaboration deal…” – Reuters

    In its press release, Pfizer maintains:
    “The FDA-approved COMIRNATY® (COVID-19 Vaccine, mRNA) and the EUA-authorized Pfizer-BioNTech COVID-19 Vaccine have the same formulation and can be used interchangeably to provide the COVID-19 vaccination series. An individual may be offered either COMIRNATY® (COVID-19 Vaccine, mRNA) or the Pfizer-BioNTech COVID-19 Vaccine to prevent coronavirus disease 2019 (COVID-19) caused by SARS-CoV-2.”

    In the same press release, we find out the Comirnaty concoct is scientifically identified as BNT162b2. Like the afore-mentioned program BNT162, version ‘b2’.
    It’s the same one as in the US EUA, so, officially, the EUA and the full approval (BLA) are awarded to the same formulation indeed, we can get that out of the way.

    However, the European EUA doesn’t mention any of the formulation, so we cannot know what they used there. A German government website does mention b2, EMA (the European FDA) doesn’t anywhere, or I haven’t found it yet.

    Let’s have a look at ‘b1’:
    COVID-19 vaccine BNT162b1 elicits human antibody and T H 1 T cell responses
    And here we find out that serial number corresponds to the lipid naono-particles formulations. So e found at least two different formulations:
    Phase I/II study of COVID-19 RNA vaccine BNT162b1 in adults
    The full approval is for BNT162b2.
    Well, CDC is the one to bring clarity this time:
    https://www.cdc.gov/vaccines/acip/meetings/downloads/slides-2020-08/Pfizer-COVID-19-vaccine-ACIP-presentation-508.pdf
    Confirmed: they had four formulations, they picked b2 version but they interchanged and cherry-picked the trial data as needed: they licensed b2 in US based on German trials made with b1 and so forth.

    And when you think “this is it”, it’s never it:
    Looks like FDA itself picked b2 and knew the trial data is mixed up between formulations, had no problem with it, more so, I discovered there were even more versions used in trials, such as b3c and so forth. Don’t believe me, check page 15 in this FDA document (PDF), as pictured at the top of the article!

    One question remains: Comirnaty as commercial name has long been used in EU, maybe not much in ads or mainstream media for decerebrated plebs, but in anything more technical than that. Why not in US, if they used the same formulation?
    Symmetrically, EU used the name, but no so sure about the b2 formulation.

    And after all this, no one can be certain what formulation they actually put in the vials.
  4. Cominarty has been approved based on only two trial studies that end 2023. It has about a dozen more to complete, as stated in the letter. I don’t see how that can be legal, but if it is, the data can change by the end of the studies, at least theoretically, which means the legal basis for the approval may very well evaporate.

    In a sane world, the Pfizer approval blunder would be the medical equivalent of the Afghanistan ‘blunder’.
    Forget about informed consent, safety, data… all they have is more guns. Which brings me to…
  5. The US Government, like most others, has left legality in March 2020 and not governing. There are dozens of known old meds that can treat these respiratory problems labeled as Covid, more are screened and discovered, there was no evidence of a new virus, at least at the time when they introduced the Emergency state. So the Emergency, the government instating it and everything that started with it is illegal and an act of terrorism. So US doesn’t have a government, but a terrorist organization holding it hostage. Nothing they did after March 2020 is remotely legal, both Trump and Biden should stand in the accused box at Nuremberg 2 now. But sleepy ghosts are changing bed sides dreaming they wake up as people who still hold a little control over their lives.
    In fact, all this is held together solely by the gun, military superiority, and psychological abuse, legal talk is 200% off and it’s just deepening the mass-hypnosis.
    There is no law but the gun, if the government didn’t have a laser point on each forehead, it wouldn’t even exist at this point.
    It’s bare war.
    If you’re not ready to internalize reality, you are not ready to change it.
  6. What the cover pic says. Then check this out!
SOURCE
SOURCE

Marion. F. Gruber, PhD
Director, Office of Vaccines Research & Review
FDA/CBER
10903 New Hampshire Ave, Building 71, Rm. 3230
Silver Spring, Maryland 20993, USA
Tel: + 1 301 796 1856
e-mail: marion.gruber@fda.hhs.gov

SOURCE

UPDATE SEPT 2, 2021:

THE FDA GRUBER RESIGNS LEAVING THE PFIZER GRUBER ORPHANED
I BET MY ASS SHE’S AVOIDING RESPONSIBILITY FOR THE WAY SHE HAS OVERSEEN THE PFIZER APPROVALS

CHD reports:

<<Two of the U.S. Food and Drug Administration’s (FDA) top vaccine regulators will leave the agency this fall, raising questions about the Biden administration and the way it sidelined the agency.

According to an email sent by Dr. Peter Marks, director of the FDA’s Center for Biologics Evaluation and Research (CBER), to staff members Tuesday, Dr. Marion Gruber, director of the FDA’s vaccines office, will quit at the end of October, and her deputy, Dr. Philip Krause, will leave in November.

Gruber and Krause were upset about the Biden administration’s recent announcement that adults should get a COVID booster eight months after they received a second shot, people familiar with the decision told The New York Times.

Neither believed there was enough data to justify offering booster shots yet, the sources said, and both viewed the announcement, amplified by President Biden, as pressure on the FDA to quickly authorize them.

Officials within the FDA were stunned by the news, CNN reported. One source described it as a “big loss” for the FDA and noted it caught leadership off guard.ORDER TODAY: Robert F. Kennedy, Jr.’s New Book — ‘The Real Anthony Fauci’

Marks said he would serve as the acting director of the vaccines office while the agency searched for its next leader.

FDA Spokeswoman Stephanie Caccomo said the agency was “confident in the expertise and ability of our staff to continue our critical public health work.”

However, a former senior FDA leader told Endpoints News, Gruber and Krause are departing because they’re frustrated the Centers for Disease Control and Prevention (CDC) and its advisory panel — the Advisory Committee on Immunizations and Practices (ACIP) — are involved in decisions they think should be up to the FDA.

The source said he heard Gruber and Krause were upset with Marks for not insisting those decisions be kept inside the FDA, and with the White House for getting ahead of FDA on booster shots.

“These two are the leaders for biologic [vaccine] review in the U.S.,” wrote Rick Bright, former director of the Biomedical Advanced Research and Development Authority, weighing in on the news. “They have a great team, but these two are the true leaders of CBER. A huge global loss if they both leave,” Bright said.

“Dr. Gruber is much more than the director,” Bright added. “She is a global leader. Visionary mastermind behind global clinical regulatory science for flu, Ebola, Mers, Zika, Sars-CoV-2, many others.”>>

Anyone who thinks she sweated harder than Trump for Pfizer’s approval, but all of a sudden had a change of mind and decided to sabotage the boosters is a baby. She’s hiding from justice.

I made this in June 2020. The Grubers are many.

I hope this helped, if anything, I’ll add it here.

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ORDER

Selling oregano for weed to kids in parking lots does more good and is more honorable than this lowest-level con job.

FDA approval letter (PDF)
Trial 1
Trial 2

Biden: “They looked at mountains of data”.

No words…

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Just like your whole government and ruling class

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Sometimes my memes are 3D. And you can own them. Or send them to someone.
You can even eat some of them.
CLICK HERE

Trump knows much more about the pandemic than he lets you know he knows.

AND THEN…

Hundreds of Native American tribes that have suffered disproportionately high addiction and death rates during the opioid epidemic agreed on Tuesday to a tentative settlement of $590 million with Johnson & Johnson and the country’s three largest drug distributors.

Together with a deal struck last fall between the distributors and the Cherokee Nation for $75 million, the tribes will be paid a total of $665 million. Purdue Pharma has already committed at least tens of millions more to the tribes in a settlement that is in mediation.

“We are not solving the opioid crisis with this settlement, but we are getting critical resources to tribal communities to help address the crisis,” said Steven Skikos, a top lawyer for the tribes.

Native Americans have endured disproportionately high opioid-related overdose deaths, by many metrics. In 2016, for example, Oglala Lakota County in South Dakota, home to the Oglala Lakota tribe, had an opioid-related death rate of 21 people per 100,000, more than twice the state average. According to one study, pregnant American Indian women were as much as 8.7 times more likely than pregnant women from other demographic groups to be diagnosed with opioid dependency or abuse.

The contours of the new settlement, announced in the U.S. District Court in Cleveland, the seat of the national opioid litigation, are similar to an agreement that the companies struck with state and local governments last summer.” – NYT

Trump praising Woody Johnson for how much cash he has

Also check

TRUMP’S MOROCCAN “VACCINE CZAR”: WORKED FOR BILL GATES, GOOGLE, GSK. WORKED IN CHINA. TRANSHUMANIST. LOCKDOWN FANATIC

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ORDER

New from your favorite coincidence-theories magazine:
There’s two timelines here that seem to meet somewhere in the recent past.

#1

CDC has just announced retiring Covid PCR tests, starting from 2022 because they can hardly tell Covid from Flu. Where Covid is caused by a virus that no one has seen in full, purified and isolated form:

We all knew that, last summer I even made a meme where I coined the term “PCRdemic”.
But just imagine how “based” their Delta Variant detection must be then!
And someone was found already preparing for this, while the plebs are shocked by the admission or not even processing it.

#2

Only weeks before this announcement, media just whispered about the new unholy alliance between Soros and Gates, who suddenly decided to buy together a major UK Covid test maker.

I mean, when did this type of prescience ever happen before, right?
(WORLD BANK SAYS COVID-19 TEST KITS ARE BEING SOLD SINCE 2017)

This alliance has a legal and formal representation as the Global Access Health (GAH), something very similar to GAVI, but focused on pillaging Africa, South America and South-Asia.


Only months before this announcement, Soros and Gates became some of the most downvoted personalities in the Northern Hemisphere, with very little competition and no benefits for the public image of the Great Reset. Meanwhile, I was writing on HOW BILL GATES AND BANKSTERS GANGED UP TO TAKE MOROCCO. AND NOW ARE RUINING IT..


Only years before that, teachers and intellectuals in US were marching against Gates’ medical and food machinations in Africa.


A decade before that, Bill Gates Sr. and George Soros could be seen shoulder to shoulder promoting Democratic Party’s fiscal policies.

Watch the full thing, a rare recording I just dug up


And so forth… as far as we’re willing to dig we find ourselves entrapped and enslaved by the same inbred class that wages now a class war against the lower classes under various guises.



Every conspiratorial correlation comes with two options: conspiracy theory (causative) or coincidence theory (non-causative). I’m too experienced to hesitate here.

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ORDER

They knew about everything else, years ahead sometimes, so of course they’ve been aware of the jabs side-effects too…
By means of hiding these from us, they actively infringed upon our right to informed consent, as per the Nuremberg Code.

FDA Safety Surveillance of COVID-19 Vaccines :
DRAFT Working list of possible adverse event outcomes
Subject to change

 Guillain-Barré syndrome
 Acute disseminated encephalomyelitis
 Transverse myelitis
 Encephalitis/myelitis/encephalomyelitis/
meningoencephalitis/meningitis/
encepholapathy
 Convulsions/seizures
 Stroke
 Narcolepsy and cataplexy
 Anaphylaxis
 Acute myocardial infarction
 Myocarditis/pericarditis
 Autoimmune disease
 Deaths
 Pregnancy and birth outcomes
 Other acute demyelinating diseases
 Non-anaphylactic allergic reactions
 Thrombocytopenia
 Disseminated intravascular coagulation
 Venous thromboembolism
 Arthritis and arthralgia/joint pain
 Kawasaki disease
 Multisystem Inflammatory Syndrome
in Children
 Vaccine enhanced disease

TAKEN FROM:

DOWNLOAD PDF

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I survived many tough times focusing on the humor in them. And I find this highly amusing. But even more disturbing, when I look around and I see most people don’t flinch hearing such a claim.

Source

As for insurances and vaccines, the topic of that Forbes article… oh boy, oh boy… Check this out! And then THIS!

Follow up:

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Sometimes my memes are 3D. And you can own them. Or send them to someone.
You can even eat some of them.
CLICK HERE