January 23, 2021
by Brian Shilhavy
Editor, Health Impact News

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 data covers 7,844 cases, including 181 deaths.

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.

Read the rest of this article at the link below . . .