Daily Clout (Naomi Wolf): "Forty-Four (44%) Percent of the Pregnancies in a Pfizer Study Ended in Miscarriages. Pfizer Misleadingly Reclassified Them
by Paul Alexander
August 12, 2022 • by Berberine on Gettr
‘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, 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, 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.
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…
The FDA had access to this data by April 1, 2021. The agency knew that a significant percentage of pregnancies ended in ‘Abortion Spontaneous,’ yet it seems to have 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. And, certainly, the FDA failed to inform the public of this very serious adverse event. Without that information, women were not able to give informed consent for receiving Pfizer’s mRNA COVID vaccine.’
Wolf et al. prompts us to ask the relevant questions:
How did Pfizer determine their experimental vaccine product did not cause the miscarriages?
What ‘Other’ causes did Pfizer identify, and how did it identify them?
Did the FDA and Centers for Disease Control and Prevention (CDC) simply accept the miscarriages as unrelated to the product, or did they demand information on those ‘Other’ causes?
And, crucially, what happened to the pregnancies which were ongoing at the report cut-off date of March 13, 2021? Were healthy babies born? Were damaged babies born? Were there more miscarriages?’