EXPLOSIVE - Pfizer Documents Exposed

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April 1, 2022, another batch of 11,000 Pfizer documents were released by the U.S. Food and Drug Administration. Pfizer trial data reveal natural immunity was as effective as the jab, and that shot side effects were more severe in those under 55.

With another batch of 11,000 Pfizer documents, released April 1, 2022, old suspicions have gained fresh support. As reported by “Rising” cohost Kim Iversen (video above), the first bombshell revelation is that natural immunity works, and Pfizer has known it all along.

The clinical trial data showed there was no difference in outcomes between those with previous COVID infection and those who got the shot. Neither group experienced severe infection. Natural immunity was also statistically identical to the shot in terms of the risk of infection.

Younger Adults More Likely to Experience Side Effects

The second revelation is that side effects from the shots were more severe in younger people, aged 18 to 55, than those aged 55 and older. (The risk of side effects also increased with additional doses, so the risk was higher after the second dose than the first.)

As many of us have said all along, the risk of severe COVID is dramatically lower in younger people than those over 60, which makes an elevated risk of side effects unacceptable.

As noted by The Naked Emperor on Substack, “with a vaccine that is producing more frequent and more severe reactions and adverse events in younger individuals, the vaccine should have been restricted to those who were actually at risk of severe COVID-19.”

Pfizer Documents Show High Rate of Myocarditis
Interestingly, Pfizer’s documentation also includes medical information that mainstream media and fact checkers have labeled as misinformation or disinformation. A pediatric consent form lists several possible side effects, including a myocarditis rate of 10 in 100,000 — far greater than the 1 in 50,000 (i.e., 2 in 100,000) rate previously reported.

Antibody-Dependent Enhancement Has Not Been Ruled Out
Many who have warned about the possibility of mRNA shots causing antibody-dependent enhancement (ADE) — a situation in which you end up being more susceptible to serious infection than you would have been otherwise — have been smeared and demonized by media and labeled as disinformation spreaders.

Yet Pfizer’s own consent form clearly states: “Although not seen to date, it cannot yet be ruled out that the studied vaccine can make a later COVID-19 illness more severe.” As noted by Iversen, if ADE truly was of no concern at all, the consent form would not include it. Yet there it is.

Vaccine-associated enhanced disease (VAED) is also listed as an “Important Potential Risk” in Table 5 on page 11 of a document called “5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports.”

As of February 28, 2021, Pfizer had 138 cases of suspected VAED, 75 of which were severe, resulting in hospitalization, disability, life-threatening consequences or death; a total of 38 cases turned out to be lethal and 65 remained unresolved.

Moreover, as noted by the Daily Expose, “Phase 3 clinical trials are designed to uncover frequent or severe side effects before a vaccine is approved for use, including ADE. But herein lies the problem, [because] none of the COVID-19 vaccines have completed Phase 3 trials.”

Pfizer Knew About Immunosuppression
Another revealing statement found in the documents is this:

“Clinical laboratory evaluation showed a transient decrease in lymphocytes that was observed in all age and dose groups after Dose 1, which resolved within approximately one week …”

In other words, Pfizer knew that, in the first week after the shot, people of all ages experienced transient immunosuppression, or put another way, a temporary weakening of the immune system, after the first dose.

Fully Vaxxed Are More Likely to Die From COVID
The fact that Pfizer and the U.S. Food and Drug Administration were aware the shot caused immunosuppression is incriminating, now that U.K. government data show that, compared to the unvaccinated, those who have received two doses are:

· Up to three times more likely to be diagnosed with COVID-19

· Twice more likely to be hospitalized with COVID-19

· Three times more likely to die of COVID-19

The Pfizer documents admit there was a temporary drop in immune function after the first dose, but the real-world data showing an increased risk of severe infection and death due to COVID among the double jabbed suggest ADE may indeed be at play later on as well.