The FDA announced a removal of the Emergency Use Authorization of the COVID vaccine. The FDA and Pfizer knew of serious safety signals before the Emergency Use Authorization. Pfizer’s own early safety review, the “5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of BNT162b2” dated February 2021, catalogued more than 42,000 adverse event reports with nearly 160,000 individual events in just the first three months. Pfizer concluded that none of these “were consequential enough” to hold back approval. The FDA went along with it. Now, with independent science repeatedly confirming risks of myocarditis, pericarditis, and waning effectiveness, there is action.
The slogan “safe and effective” became the government’s mantra, repeated endlessly while concerns were dismissed as fringe. Yet large-scale studies now show otherwise. The Lancet published evidence of elevated myocarditis risk in young men. Nature Communications confirmed that even the dosing interval influenced heart inflammation outcomes. Multiple NEJM and JAMA reports documented that protection against infection dropped below 20% after just six months. This is not a profile of safety or effectiveness; it is a failed medical product. To continue marketing it under false pretenses while evidence piles up is a dereliction of duty by both regulators and pharmaceutical executives who cashed in at the expense of public health.
Worse yet, Pfizer and federal agencies had the data in hand. Their confidential February 2021 report detailed tens of thousands of adverse events across multiple organ systems. Yet they waved it away as inconsequential. Independent researchers, re-analyzing the same trial data, later found a 3.7-fold increase in cardiovascular deaths among the vaccinated compared to placebo. Other peer-reviewed papers have confirmed pregnancy complications, menstrual irregularities, and disproportionate cardiac risks in young males. These are not side effects “rare enough to ignore.” They are red-flag signals that should have stopped the rollout in its tracks. Instead, Americans became unwitting subjects in a massive, uncontrolled experiment. Even those who earnestly researched before getting the shot, were acting off of severely flawed information.
With former skeptics now leading efforts to phase out the vaccine, the writing is on the wall. But why just a partial ban? Every additional day this is allowed means more people exposed to risks that government officials and corporate leaders knew about from the start. The Pfizer website to this day downplays the side effects of its COVID shot and says that health concerns are rare. Paul’s warning in Galatians 6:7 comes to mind: “Do not be deceived: God is not mocked, for whatever one sows, that will he also reap.” We have reaped disastrous results from the sowing of deceptive seeds. It’s time to reap honesty, not deception; transparency, not concealment. While the FDA move is in the right direction, the COVID vaccine should be banned sooner rather than later. Anything less just prolongs the, say it with me…Stupidocrisy.
Sources
- 5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of BNT162b2. (Feb 2021) PDF
- Wong HL, Hu M, et al.The Lancet (2022). Link
- Stowe J, Andrews N, et al.NEJM (2022). Link
- Menegale N, et al.JAMA Netw Open (2023). Link
- Le Vu S, et al.Nature Communications (2024). Link
- Jaiswal V, et al.ScienceDirect (2023). Link
- Takada K, et al.Scientific Reports (2025). Link
- Arashiro T, et al.Clinical Infectious Diseases (2023). Link
- Wu N, et al.Lancet Resp Med (2023). Link
- Ioannidis JPA, et al.JAMA Health Forum (2025). Link
- Myocarditis and Pericarditis after mRNA COVID-19 Vaccination (2024). Link
- Fraiman J, et al.Vaccine (2022). Serious Adverse Events of Special Interest Following mRNA Vaccination. Link
