The FDA KNEW: 18% of pregnant women miscarried following COVID-19 gene therapy, but therapeutics were given Emergency Use Authorization [despite the alarming rate of fetal manslaughter].
UPDATE: A correction has been issued on this topic regarding the original claim that Pfizer adverse event documents revealed that 44% of pregnant women who received the vaccine suffered a miscarriage (spontaneous abortion).
Multiple analysts have further reviewed and cross-checked the recently released documents and discovered that the number of women who experienced spontaneous abortions was 11, not 22, as originally reported, with adverse events being counted twice by mistake.
In making the decision to grant Emergency Use Authorization (EUA) to Wuhan coronavirus (COVID-19) “vaccines,” the U.S. Food and Drug Administration (FDA) knew full well at the time that nearly a [fifth] of all pregnant women would [spontaneously abort] as a result of the injections.
- The latest Pfizer document drop shows that 18 percent of all pregnant women who participated in Pfizer’s mRNA (messenger RNA) jab trials ended up losing their [unborn children]. To the FDA, this still constitutes a “safe and effective” drug.
(Related: Wisconsin doctor who [lauded] COVID-19 [gene therapy] suffered a spontaneous abortion after [receiving] hers.)
After these women lost their children, Pfizer tried to claim that the deaths had nothing to do with its shots. The FDA apparently took Pfizer’s word for it and proceeded to authorize, and later approve, the injections as a remedy for the Fauci Flu.
The thousands upon thousands of pages of documents that Pfizer and the FDA tried to conceal for 75 years demonstrate a shocking pattern of intentional deceit by the two entities. Both Pfizer and the FDA have been working overtime to try to withhold the truth from the public – but that truth is now coming out.
Big Pharma and the FDA are LIARS
Unfortunately for the millions of women who already took the jabs, the damage is already done. Many have already learned the hard way that Operation Warp Speed is really just [Operation Quick Kill], including for unborn [citizens].
The women who participated in the Pfizer trial all took between one and four injections of Pfizer’s mRNA [COVID-19 gene therapy]. Forty-two received the drug immediately while eight received a placebo initially followed by the real drug later.
By March 31, 2021, all of the pregnant women in the trial – 50 in total – had taken at least one dose of Pfizer’s BNT162b2 experimental injectable gene therapy. The following explains how Pfizer knowingly [obfuscated] the disastrous [trial] results.
- “Pfizer notes the miscarriages as serious adverse events (SAEs) with ‘moderate’ (2) or ‘severe’ (3) toxicity ratings. However, all the miscarriages were reported as being unrelated to the trial vaccine – i.e., having ‘Other’ causes – and marked as ‘Recovered / resolved’ adverse effects. To reiterate, not only does Pfizer deny any vaccine-related causality and assert the losses of life had other causes, but it also categorizes losing a baby as a ‘resolved adverse effect’ – like a headache that went away.”
In other words, the loss of a pregnancy is just collateral damage – a “side effect” that quickly got “resolved” once the [inbound citizen] died. This is how Pfizer operates, by the way: just hide the truth, recategorize it, or flat-out lie about it – and the FDA does the exact same thing.
By April 1, 2021 the FDA was fully aware of the fact that a “significant percentage” of pregnant women who were [treated with the gene therapy] for the Fauci Flu suffered “spontaneous abortion.” Even so, the agency proceeded to do nothing, allowing many more pregnant women to receive the [proscribed treatment].
- The FDA “failed in its duty to study the data and investigate what basis Pfizer had for marking the fetal deaths as unrelated to the vaccine and having ‘Other’ causes,” reports explain.
The FDA also failed to at least tell the public that there is a serious risk involved for unborn babies who are exposed to covid shots via their mothers. Without that information, notes the Daily Clout, “women were not able to give informed consent for receiving Pfizer’s mRNA COVID-19 [gene therapy].”
To say that the FDA failed implies that it simply made a mistake, which is not the case. The corrupt federal agency lied on behalf of Pfizer by withholding the truth from the public, which is a crime against humanity as well as a dereliction of duty.
More stories like this one can be found at ChemicalViolence.com.
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