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August 22, 2022 at 7:16 pm

Multiple Pregnancies in a Pfizer Trial Ended in Miscarriages. Pfizer Misleadingly Reclassified Them…

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by Bererine on Gettr at Daily Clout

A Pfizer adverse events document, part of the court-ordered disclosure of documents  released by the Food and Drug Administration (FDA) on July 1, 2022, reveals chilling data regarding harm to pregnancies.  A stunning 44% percent* of pregnant women participating in Pfizer’s mRNA COVID vaccine trial suffered miscarriages. [125742_S1_M5_5351_c4591001-interim-mth6-adverse-events.pdf, https://pdata0916.s3.us-east-2.amazonaws.com/pdocs/070122/125742_S1_M5_5351_c4591001-interim-mth6-adverse-events.zip]

A section of the document, on page 3643, titled  Listing of Subjects Reporting Pregnancy After Dose 1, reveals that fifty women became pregnant during the Pfizer trial. However, one must dig through the rest of the large document to learn the disturbing fact that twenty-two* of these 50* women suffered “Abortion Spontaneous,” “Abortion Spontaneous Complete,” “Abortion Spontaneous Incomplete,” or “Miscarriage.” [pp. 219, 561, 708, 1071, 1146, 1179, 1349, 1749, 1758, 1806, 1809, 3519, 3526, 3560, 3536, 3537, 3538, 3536, 3547, and 3551.]

The adverse events report cut-off date for this study was March 13, 2021, and the FDA received the report from Pfizer on April 1, 2021.

Thus, the US FDA has been aware of the horrifying rate of fetal death suffered by pregnant women injected with Pfizer’s mrna vaccine, since the start of April 2021. But the FDA made no warning announcement to the pregnant women of America. 

How did these miscarriages come about?

The pregnant women included in Listing of Subjects Reporting Pregnancy After Dose 1 received between one and four Pfizer MRNA vaccine injections each. 42 of the women received the trial drug right away. Eight received the placebo and were then unblinded and given the vaccine. So, by March 31, 2021, all the pregnant women in the trial had received Pfizer’s BNT162b2 version of the vaccine.

Pfizer notes the miscarriages as serious adverse events (SAEs) with ‘moderate’…

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