40% of pregnant women who participated in Pfizer vaccine trial suffered miscarriages in US: Report
According to an analysis of the documents, out of 50 pregnant women, 22 them lost their babies. Feminist author and journalist Dr. Naomi Wolf revealed this information on Steve Bannon’s War Room podcast.
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Washington DC, August 18: It major blow to the liberals who wanted the Indian government to import Pfizer as according to internal Pfizer documents, recently released under court order, more than 40 percent of pregnant women who participated in Pfizer’s mRNA COVID vaccine trial suffered miscarriages.
According to an analysis of the documents, out of 50 pregnant women, 22 them lost their babies. Feminist author and journalist Dr. Naomi Wolf revealed this information on Steve Bannon’s War Room podcast.
It should be noted that Wolf has been spearheading research and analysis of the Pfizer documents through her website Daily Clout. During the podcast, Wolf said the adverse event cutoff report showing the miscarriages was March 13, 2021, and the Food and Drug Administration (FDA) received the report on April 1, 2021.
She further targeted FDA for remaining silent despite knowing the truth. "FDA was aware of the horrifying rate of fetal death by the start of April 2021 and were silent," she said.
Wolf further also pointed out that the Pfizer trial data correlates with the massive increase in miscarriages seen worldwide since the vaccine rollouts. Shockingly, the CDC, as recently as last month, still recommended the experimental mRNA vaccines for pregnant and breastfeeding “people.”
In a January court ruling, U.S. District Judge Mark Pittman of the Northern District of Texas ordered the FDA to release around 12,000 documents immediately, and then 55,000 pages a month until all documents were released, totaling more than 300,000 pages.
The nonprofit group, Public Health and Medical Professionals for Transparency, sued the FDA last September after the agency denied its Freedom of Information Act (FOIA) request to expedite the release of mRNA vaccine review documents. In a November 2021 joint status report, the FDA proposed releasing only 500 pages of the documents a month, which would have taken up to 75 years.
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