Documents used by Moderna for Food and Drug Administration (FDA) emergency use approval of the COVID “vaccine” indicate both the Moderna and the FDA knew of the dangers posed by the mRNA experimental drug. Some 13,685 pages related to Moderna’s COVID 19 clinical trials were released by the FDA as part of the Freedom of Information Act lawsuit by Dallas-based nonprofit Defending The Republic (DTR). Some 16 deaths were documented in the aftermath of taking the experimental serum. Moderna, however, conducted autopsies on only two and listed the cause of death for the vast majority as “unknown.” DTR stated that Moderna purposely decided not to investigate the cause of deaths.
Notwithstanding, those running the studies concluded that the deaths were unrelated to the Moderna serum. DTR said, “There were numerous examples of participants with post-vaccination Bell’s Palsy and Shingles (Herpes Zoster). One 44 year-old female had “left side facial paralysis” just eight days after the second dose. Numerous vaccinated participants saw the onset of Shingles less than 10 days after vaccination. Other key observations during the Moderna “studies” involved serious adverse events for those in the vaccinated groups. A number of participants experienced: myocardial infarction (heart attack); pulmonary embolism; spontaneous abortion/miscarriage; transient ischemic attack (TIA); and lymphoma.”
In January 2022, The Daily Jot obtained a similar confidential report by Pfizer to the FDA. The report, “5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021,” indicates as of February 28, 2021 there were 42,086 reports of 158,893 adverse events from the Pfizer COVID vaccine—all withheld from the public. Some of the results: “Pregnancy outcomes for the 270 pregnancies were reported as spontaneous abortion (23), outcome pending (5), premature birth with neonatal death, spontaneous abortion with intrauterine death (2 each), spontaneous abortion with neonatal death, and normal outcome (1 each).”
Other results included: Anaphylaxis in 54% of the relevant cases retrieved, four causing death, and Pfizer concluded that the data “did not reveal any significant new safety information,”; Lack of efficacy was found in 3.9% of the database; 3.3% of the total database developed cardiovascular adverse reactions, Of the reported cases, “136 (9.69%) were fatal.” Again, Pfizer concluded: “This cumulative case review does not raise new safety issues.” Facts are that the US government knew all along that this serum was neither safe, nor effective, yet it conspired with big business and media to coerce Americans to take it, while censoring those who warned against it. This is criminal. Let us plead Amos 5:24 to our Lord that “justice run down as waters and righteousness as a mighty stream.”
NOTE: If you have been vaccinated and experience any of the aforementioned symptoms, all is not lost. You can detox and neutralize/minimalize the effects of the spike proteins caused by the shots. Truth for Health Foundation (www.truthforhealth.org/patientguide/ ) also has treatment guides and can assist you in locating a doctor that understands the side effects of the COVID shot and can recommend an effective protocol. It is important that you take control and develop a comprehensive health strategy.
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