FDA Knew 44% of Pregnant Women in Pfizer Trial Suffered Miscarriages

It is indisputable that neither Pfizer nor the U.S. Food and Drug Administration (FDA) is at all concerned about adverse events related to Pfizer’s clinical trial data. After all, they sought to hide it from the general public for 75 years. While blatantly unacceptable, the fact both parties knew that 44 percent of pregnant women participating in the Pfizer mRNA COVID-19 “vaccine” trial suffered miscarriages is immoral and seems incredibly corrupt.

Shockingly, as the FDA releases Pfizer trial data each month per court order, a Pfizer adverse events report transferred on July 1, 2022, reveals that after the women lost their babies, the billion-dollar big pharma giant reported that the heartbreaking miscarriages were unrelated to the trial. The volunteer team at Daily Clout discovered the intentional deceit by scouring through the thousands upon thousands of Pfizer trial documents released each month that form the rationale behind the FDA’s emergency use authorization (EUA) and subsequent August 23, 2021, “approval” of Pfizer’s mRNA COVID-19 “vaccine” product.

According to an article in Daily Clout, the women listed in Listing of Subjects Reporting Pregnancy After Dose 1 each received between one and four of Pfizer’s mRNA injections. Forty-two received the trial drug right away, and eight received the placebo and were then unblinded and given the vaccine. Thus, by March 31, 2021, all of the pregnant women in the trial—there were 50 of them—had received Pfizer’s BNT162b2 version of its experimental “vaccine.” Summarizing Pfizer’s deceptive efforts after the miscarriages, the article explained:

“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.”

Screenshot / Pfizer Data / Listing of Subjects Reporting Pregnancy After Dose 1

With access to this startling data by April 1, 2022, the article points out that the FDA was aware that a “significant percentage of pregnancies ended in ‘Abortion Spontaneous.'” Yet, despite this, the agency “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.” Moreover, the FDA failed to inform the public of this life-changing, serious adverse...

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