Mercola: FDA and Pfizer Knew COVID Shot Caused Immunosuppression

Similarly, in August 2021, when Comirnaty was licensed, Dr. Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases, claimed the COVID jab was safe during pregnancy:

The American College of Obstetricians and Gynecologists (ACOG) also make definitive statements about safety, claiming “Vaccination may occur in any trimester, and emphasis should be on vaccine receipt as soon as possible to maximize maternal and fetal health.”² Yet even the Comirnaty label^3,4 states that “available data on Comirnaty administered to pregnant women are insufficient to inform vaccine associated risks in pregnancy.”

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.”⁵

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.^6,7

Moreover, as noted by the Daily Expose,⁸ “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’s Phase 3 trial is due to be completed February 8, 2024⁹ — nearly two years from now! Despite that, Pfizer concluded in its FDA submission that “None of the 75 cases could be definitively considered as VAED.”

“[H]ow on earth could they not definitively conclude that VAED was to blame when 75% of the confirmed ‘break-through’ cases reported to them were severe disease resulting in hospitalization, disability, life-threatening consequences of death?” The Daily Expose asks.¹⁰

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.

As noted by Iversen, this may have skewed infection rates, as people were not considered partially vaccinated until 14 days after their first shot,¹¹ and officially fully vaccinated two weeks after the second dose.

If people are susceptible to infection during that first week, yet are counted as unvaccinated during that time, this makes it appear as though the unvaccinated are more prone to infection when that’s simply not true. Pfizer’s own trial showed infection was significantly more common in the vaccine group than the placebo group — 409 versus 287 — within the first seven days of the jab.¹²

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:¹³

• 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.

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