Vaccine killed 1,200 in first 90 days of rollout.

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The FDA asked a federal court for a ridiculous 55-year timespan to release all of the documentation on the Pfizer COVID shots to the public. Fortunately, that judge refused and has demanded that the FDA start releasing all the info right now.

The first batch of documents have now been released and show that during the first 90 days of the vaccine rollout (December 2020 to February 2021), there were tens of thousands of adverse reactions to the shots recorded and more than 1,200 people were killed. Yet for some reason, the FDA refused to yank the shots out of circulation.

The FDA only recorded serious adverse reactions to the injections of Pfizer’s vaccine, which was created in part using harvested kidney cells from aborted babies. 51,335 people suffered serious general disorders and administration site conditions; 25,957 people suffered nervous system disorders; 17,283 people suffered musculoskeletal and connective tissue disorders; 8,476 suffered skin and subcutaneous tissue disorders; 8,848 people suffered respiratory, thoracic and mediastinal disorders; 4,610 suffered from infections and – good grief – parasitic infestations (???); 5,590 people suffered from poisoning, injury and procedural complications; and 1,223 people flat-out died from being injected with the vaccine.

The FDA knew that all this had happened in the first three months of the vaccine rollout, and had compiled all that data on adverse reactions, deaths and parasitic infestations by April of 2021. Just as a reminder, the experimental swine flu vaccine that was rushed to market in 1976 was yanked from the market after it killed just 25 Americans.

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