top of page

Naomi Wolf: "Forty-Four (44%) Percent of the Pregnancies in a Pfizer Study Ended in Miscarriages

Pfizer Misleadingly Reclassified Them.

‘A Pfizer adverse events document released by the Food and Drug Administration (FDA) on July 1, 2022, reveals chilling data showing 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,] A section of the document, on page 3643, called Listing of Subjects Reporting Pregnancy After Dose 1, shows that 50 women became pregnant during the trial. However, one must dig through the rest of the large document to learn that 22 of the 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 was March 13, 2021, and the FDA received the report from Pfizer on April 1, 2021. Thus, the FDA was aware of the horrifying rate of fetal death by the start of April 2021.

The women listed in Listing of Subjects Reporting Pregnancy After Dose 1 received between one and four 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.


bottom of page