Health & Environment, Politics

Docs Reveal Surge in Miscarriages, Stillborns Post-Vaxx

When a group called Public Health and Medical Professionals for Transparency asked Pfizer to share the raw data from their COVID vaccine trials and post-marketing surveillance that was used to license the injection, the pharma giant linked up with the Food and Drug Administration (FDA) to refuse the Freedom of Information Act (FOIA) requests. In fact, the FDA (meant to serve and protect public health) hired Justice Department lawyers and went to court to shield the pharmaceutical giant from having to reveal its data – for 55 years. That’s right. The FDA and Pfizer did not want anyone to see the numbers behind their COVID vaccine until 2076.

Fortunately, a judge ruled that the FDA and Pfizer would have to answer their FOIA requests. Among the first reports handed over by Pfizer was a “Cumulative Analysis of Post-authorization Adverse Event Reports” describing events reported to Pfizer up until February 2021. It reveals that the drug behemoth received more than 150,000 serious adverse event reports within three months of rolling out its COVID shot, but here we will focus on Table 6 of the data on pregnant and lactating women who received the shots in the first few months of the rollout, which began December 11. Most of these women would have been healthcare workers because that was who the first rounds of shots went to. As the clinical trials preceding the rollout excluded pregnant women, these would have been the first pregnant and lactating women to have ever received the vaccines. Read more…

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