The gods of shitfuckery are most pleased.
Their demonic minions in media and government have laid out a trail of bat guano, hoping all will buy into their latest stench.
FDA did NOT approve Pfizer covid vaccine… Approval granted to “Comirnaty” vax that isn’t in production! – (just a scant 2 minutes to give you a bit of truth)
That’s right boys and girls, it’s another bomb of bullshit from government and media hyena’s, hoping you’ll buy into their latest outhouse of shit.
But you need more than 2 minutes from the ‘war room’ to get to the shit of it… right?
Fair enough. Here’s more….
A New Low for the FDA – via trialsitenews.com
Today, August 23, 2021, the FDA approved the Pfizer COVID19 vaccine in spite of the following issues:
The vaccines are more likely to kill you than save you. The clinical trial (gold-standard medical research) evidence to date shows the vaccine kills more people than it saves (including Pfizer’s own 6 month randomized study which demonstrated a 7% higher overall death rate for those administered the vaccine. The vaccine reduced COVID deaths by 50%, however this came at the cost of increasing deaths from cardiac arrest and other causes, so that the net benefit is negative, i.e., the vaccine is more likely to kill you than save you. For example, Pfizer’s own study showed deaths from COVID were reduced by a factor of 2, but this saving was more than offset by deaths from cardiac arrest which went up by 4X. This is not a good tradeoff. The safety data in VAERS compared with the CDC data on mortality for different age cohorts also confirms that the vaccines are more likely to harm than help.
No autopsies have ever been done in the US on patients who die after getting the vaccine to determine if the vaccine contributed to the death. It is astonishing there are 13,068 death reports in VAERS without even a single autopsy being done in the US and nobody in academia, Congress, or the mainstream media has called for autopsies. Autopsies are a huge risk for them because if they are done, people will realize just how unsafe these vaccines really are. (read more)
And this, from Robert Kennedy Jr.’s site, childrenshealthdefense.org
2 Things Mainstream media Didn’t Tell You About FDA’s Approval of Pfizer Vaccine –
Buried in the fine print of Monday’s approval by the U.S. Food and Drug Administration of the Pfizer Comirnaty COVID vaccine are two critical facts that affect whether the vaccine can be mandated, and whether Pfizer can be held liable for injuries.
The press reported that vaccine mandates are now legal for military, healthcare workers, college students and employees in many industries. New York City Mayor Bill de Blasio has now required the vaccine for all teachers and school staff. The Pentagon is proceeding with its mandate for all military service members.
But there are several bizarre aspects to the FDA approval that will prove confusing to those not familiar with the pervasiveness of the FDA’s regulatory capture, or the depths of the agency’s cynicism.
First, the FDA acknowledges that while Pfizer has insufficient stocks of the newly licensed Comirnaty vaccine available, there is “a significant amount” of the Pfizer-BioNTech COVID vaccine — produced under Emergency Use Authorization (EUA) — available for use.
Second, the FDA pointed out that both the licensed Pfizer Comirnaty vaccine, and the existing vaccine are “legally distinct,” but proclaims that their differences do not “impact safety or effectiveness.”
There is a huge real-world difference between products under an EUA compared with those that FDA has fully licensed. EUA products are experimental under U..S law.
Both the Nuremberg Code and Federal Regulations provide that no one can force a human being to participate in this experiment. Under 21 U.S. Code Sec.360bbb-3(e)(1)(A)(ii)(III), “authorization for medical products for use in emergencies,” it is unlawful to deny someone a job or an education because they refuse to be an experimental subject. Instead, potential recipients have an absolute right to refuse EUA vaccines.
U.S. laws, however, permit employers and schools to require students and workers to take licensed vaccines.
EUA-licensed vaccines have an extraordinary liability shield under the 2005 Public Readiness and Preparedness Act. Vaccine manufacturers, distributors, providers and government planners are immune from liability. The only way an injured party can sue is if he or she can prove willful misconduct, and if the U.S. government has also brought an enforcement action against the party for willful misconduct. No such lawsuit has ever succeeded.
The government has created an extremely stingy compensation program, the Countermeasures Injury Compensation Program, to redress injuries from all EUA products.
The program’s parsimonious administrators have compensated under 4% of petitioners to date — and not a single COVID vaccine injury — despite the fact that physicians, families and injured vaccine recipients have reported more than 600,000 COVID vaccine injuries.
At least for the moment, the Pfizer Comirnaty vaccine has no liability shield. Vials of the branded product, which say “Comirnaty” on the label, are subject to the same product liability laws as other U.S. products.
When the Centers for Disease Control and Prevention’s (CDC) Advisory Committee for Immunization Practices places a vaccine on the mandatory schedule, a childhood vaccine benefits from an generous retinue of liability protections.
But licensed adult vaccines, including the new Comirnaty, do not enjoy any liability shield. Just as with Ford’s exploding Pinto, or Monsanto’s herbicide Roundup, people injured by the Comirnaty vaccine could potentially sue for damages.
And because adults injured by the vaccine will be able to show that the manufacturer knew of the problems with the product, jury awards could be astronomical.
Pfizer is therefore unlikely to allow any American to take a Comirnaty vaccine until it can somehow arrange immunity for this product.
Given this background, the FDA’s acknowledgement in its approval letter that there are insufficient stocks of the licensed Comirnaty, but an abundant supply of the EUA Pfizer BioNTech jab, exposes the “approval” as a cynical scheme to encourage businesses and schools to impose illegal jab mandates.
The FDA’s clear motivation is to enable Pfizer to quickly unload inventories of a vaccine that science and the Vaccine Adverse Events Reporting System have exposed as unreasonably dangerous, and that the Delta variant has rendered obsolete.
Americans, told that the Pfizer COVID vaccine is now licensed, will understandably assume that COVID vaccine mandates are lawful. But only EUA-authorized vaccines, for which no one has any real liability, will be available during the next few weeks when many school mandate deadlines occur.
The FDA appears to be purposefully tricking American citizens into giving up their right to refuse an experimental product.
While the media has trumpeted that the FDA has approved COVID vaccines, the FDA has not approved the Pfizer BioNTech vaccines, nor any COVID vaccines for the 12- to 15-year age group, nor any booster doses for anyone.
Here’s what you need to know when somebody orders to get the vaccine:; Ask to see the vial. If it says “Comirnaty,” it’s a licensed product. If it says “Pfizer-BioNTech,” it’s an experimental product, and under 21 U.S. Code 360bbb, you have the right to refuse.
If it comes from Moderna or Johnson & Johnson (marketed as Janssen), you have the right to refuse.
The FDA is playing bait and switch with the American public — but we don’t have to play along. If it doesn’t say Comirnaty, you have not been offered an approved vaccine.
“A genius doesn’t adjust his treatment of a theme to a tyrant’s taste” ―
Tonight’s musical offering: