The Vaccine Adverse Event Reporting System (VAERS) is a U.S. Government funded database that tracks injuries and deaths caused by vaccines.
A 2011 report by Harvard Pilgrim Health Care, Inc. for the U.S. Department of Health and Human Services (HHS) stated that fewer than one percent of all vaccine adverse events are reported to the government:
Although 25% of ambulatory patients experience an adverse drug event, less than 0.3% of all adverse drug events and 1-13% of serious events are reported to the Food and Drug Administration (FDA).
Likewise, fewer than 1% of vaccine adverse events are reported. Low reporting rates preclude or slow the identification of “problem” drugs and vaccines that endanger public health. New surveillance methods for drug and vaccine adverse effects are needed. (Source.)
Currently, data from the two experimental mRNA COVID injections that have been voluntarily reported is available for a two week period from the end of December through January 13, 2021.
The largest amount of deaths occurred in people over the age of 75.
There was at least one death recorded of an unborn baby dying just after the mother received an experimental mRNA Pfizer shot while pregnant:
I was 28 weeks and 5 days pregnant when I received the first dose of the COVID19 vaccine. Two days later (12/25/2020 in the afternoon), I noticed decreased motion of the baby.
The baby was found to not have a heartbeat in the early am on 12/26/2020 and I delivered a 2lb 7oz nonviable female fetus at 29 weeks gestation. (Source.)
As we have previously reported here at Health Impact News, the guidelines for emergency use of the experimental mRNA Pfizer injection in the UK warned pregnant women, and women planning to soon become pregnant, to NOT get the experimental jab.
But the FDA guidelines issued in the U.S. for the same experimental Pfizer injection did not include such warnings. See:
When reading the accompanying notes from these cases that were reported to VAERS, it is clear that many healthcare professionals are reluctant to report these cases, probably fearing repercussions for doing so.
In some cases, family members filed the report because the healthcare facility refused to do.
(VAERS ID # 913733) My grandmother died a few hours after receiving the moderna covid vaccine booster 1. While I don’t expect that the events are related, the treating hospital did not acknowledge this and I wanted to be sure a report was made.
(VAERS ID # 914621) Resident in our long term care facility who received first dose of Moderna COVID-19 Vaccine on 12/22/2020, only documented side effect was mild fatigue after receiving. She passed away on 12/27/2020 of natural causes per report. Has previously been in & out of hospice care, resided in nursing home for 9+ years, elderly with dementia. Due to proximity of vaccination we felt we should report the death, even though it is not believed to be related.
(VAERS ID # 914895) Injection given on 12/28/20 – no adverse events and no issues yesterday; Death today, 12/30/20, approx.. 2am today (unknown if related – Administrator marked as natural causes)
Since so few reports are actually recorded in the VAERS reporting system, what is the true number of people being killed by these lethal injections? For those who are not killed, how many will be crippled or suffer autoimmune diseases for the rest of their lives?
If during pre-COVID times less than 1% of all vaccine injuries and deaths were reported to VAERS, let’s make a conservative estimate and say that because it is widely known that the COVID injections were fast-tracked to market and have not yet been approved by the FDA, that a greater percentage are being reported, like 10% of the adverse reactions, including deaths.
We are looking at a pace of nearly 1000 deaths per week by injection due to non-FDA approved mRNA injections among nearly 40,000 cases a week of injuries due to these injections.
This is a public health crisis that is 100% avoidable and 100% caused by Big Pharma and the U.S. Government!