A federal judge ordered Food and Drug Administration (FDA) compliance with a Freedom of Information Act request to disclose Pfizer data that factored into FDA’s recent decision granting the experimental mRNA vaccine an Emergency Use Authorization. The first released data recorded over 800 adverse side effects. Most alarming were acute myocardial infarction, arrhythmia, cardiac failure, cardiogenic shock, coronary artery disease, myocardial infarction, postural orthostatic tachycardia syndrome, stress cardiomyopathy, tachycardia, liver injury, facial paralysis, immune mediated/autoimmune disorders, arthritis, chronic fatigue syndrome, polyarthritis, rheumatoid arthritis, Guillain-Barre syndrome, fibromyalgia/trigeminal neuralgia, amniotic cavity infection, congenital anomaly, death neonatal, eclampsia, and fetal distress syndrome.
Pfizer’s general overview of 42,086 cases of adverse effects in ninety days found 20,112 persons recovered, 1,233 died, and the balance pended resolution.
Interesting that the FDA had no problem with those numbers.
5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021
https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf
Retain Mike wrote: “A federal judge ordered Food and Drug Administration (FDA) compliance with a Freedom of Information Act request to disclose Pfizer data that factored into FDA’s recent decision granting the experimental mRNA vaccine an Emergency Use Authorization. The first released data recorded over 800 adverse side effects.
Now how many side effects from the virus?