FDA Admits to Major Vaccine Lie

Astonishingly, the FDA admitted what most Americans with any common sense realized. The Wuflu vaccines are dangerous.

According to MarketWatch,

U.S. regulators on Thursday strictly limited who can receive Johnson & Johnson’s COVID-19 vaccine due to a rare but serious risk of blood clots.

The Food and Drug Administration said the shot should only be given to adults who cannot receive a different vaccine or specifically request J&J’s JNJ, -1.91% vaccine. U.S. authorities for months have recommended that Americans starting their COVID-19 vaccinations use the Pfizer PFE, -2.44% or Moderna MRNA, -8.40% shots instead.

FDA officials said in a statement that they decided to restrict J&J’s vaccine after taking another look at data on the risk of life-threatening blood clots within two week of vaccination.

Talk about the cops coming after the bank has been robbed. This “breaking” news is news to no one.

Still, check out how other deadly Wuflu vaccines are depicted.

The decision is the latest restriction to hit J&J’s one-dose vaccine, which has long been overshadowed by the more effective two shots from Pfizer and Moderna.

More effective two shots from Pfizer and Moderna? I suggest to the public that J&J didn’t grease enough palms to get the nod of approval regardless of actual tests. And in fact, according to the article in December, the Centers for Disease Control and Prevention recommended prioritizing the Moderna and Pfizer shots over J&J’s because of its safety issues. Previously U.S. officials had treated all three vaccines similarly because they’d each been shown to offer strong protection.

But follow-up studies have consistently shown lower effectiveness for J&J’s vaccine. And while the blood clots seen with J&J’s shot are rare, officials say they’re still occurring.

Translated: J&J was out-bid by the other two Wuflu vaccine manufacturers.

Pfizer Woes

It’s particularly interesting that Pfizer isn’t currently in the hot seat. Just last month, we reported on documents that prove Pfizer knew about adverse effects of their vaccine.  And they wanted to hide pertinent vaccine data for 80 years.

I previously wrote:

The “cure” was indeed more dangerous than the disease. Much more dangerous. The summary is as follows:

        • A small batch of documents released by the U.S. Food and Drug Administration in mid-November 2021 revealed that in the first three months of the COVID jab rollout, Pfizer received 42,086 adverse event reports that included 1,223 deaths.
        • The first really large tranche of Pfizer documents — some 10,000 pages — was released by the FDA March 1, 2022. Included are nine pages of recorded side effects, about 158,000 different health problems in all.

So Pfizer, et al knew early on that the shots were dangerous. These numbers are far greater than those needed to shut down these clinical trials. But Biden’s administration cloaked Pfizer and other snake oil manufacturers under  a blanket of immunity.

I find it quite peculiar that suddenly Pfizer’s out of the news stream and J&J is in. I hope the media slowdown in Pfizer’s case doesn’t mean ‘all is forgiven,’ because corporate greed was willing to change lives forever, by killing people. Could you forgive a big corporation for putting profits over human life? Especially if that life was one of your loved ones?

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