Posted on 03/27/2021 3:43:32 PM PDT by ransomnote
The numbers reflect the latest data available as of Feb. 12 from the CDC’s Vaccine Adverse Event Reporting System website. Of the 929 reported deaths, about one-third occurred within 48 hours.
According to new data released today, as of Feb. 12, 15,923 adverse reactions to COVID vaccines, including 929 deaths, have been reported to the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS) since Dec. 14, 2020.
VAERS is the primary mechanism in the U.S. for reporting adverse vaccine reactions. Reports submitted to VAERS require further investigation before a determination can be made as to whether the reported adverse event was directly or indirectly caused by the vaccine.
The latest VAERS data show that 799 of the deaths were reported in the U.S., and that about one-third of those deaths occurred within 48 hours of the individual receiving the vaccination.
As is consistent with previous VAERS data reports, 192 of the reported deaths — or 21% — were cardiac-related. As The Defender reported last month, the spike protein that the body is instructed to make by mRNA vaccines like those developed by Pfizer and Moderna have the potential to cause microvascular injury (inflammation and small blood clots called microthrombi) to the heart, brain, liver and kidneys in ways that were not assessed in the safety trials.
Of the 929 deaths reported since Dec. 14, 2020, the average age of the deceased was 77.8 and the youngest was 23. Fifty-two percent of the reported deaths were among men, 45% were women and 3% are unknown. Fifty-eight percent of the deaths were reported in people who received the Pfizer vaccine, and 41% were related to the Moderna vaccine.
States with the highest reported number of deaths were: California (71); Florida (50); Ohio (38); New York (31); Kentucky (41); Michigan (31); and Texas (31).
CBS Detroit reported this week that a 68-year old news anchor died one day after being vaccinated for COVID of a suspected stroke.
Reports of deaths among elderly people after being vaccinated for COVID continue to surface, including the article published this week by The Defender about 46 nursing home residents in Spain who died within one month of receiving the Pfizer vaccine.
According to the latest data, 3,126 “serious” adverse reactions have been reported. Adverse reaction reports from the latest CDC data also include:
So far, only Pfizer and Moderna vaccines — approved for emergency use, but not fully licensed — are being used in the U.S.
AstraZeneca’s COVID vaccine, which does not use mRNA technology, was approved for emergency use this week by the World Health Organization, paving the way for some countries to start using it. However, as The Defender reported this week, some nations have said they won’t use it, citing safety and efficacy concerns.
FiercePharma reported today that the FDA may reject the AstraZeneca vaccine over concerns relating to efficacy, especially against new COVID variants, and manufacturing issues.
News reports indicate that a growing number of people, including nearly 30% of healthcare workers, now say they don’t want the COVID vaccine, citing safety concerns.
The Washington Post reported this week that nearly a third of military personnel are opting out of the vaccines, and ESPN reported that top NBA players are reluctant to promote the vaccine.
Meanwhile, the FDA has not yet implemented systems to monitor the safety of the experimental COVID vaccines. FDA officials told The New York Times they don’t expect the systems to be up and running before the Biden administration reaches its goal of vaccinating 100 million Americans — nearly one third of the U.S. population.
As of Feb. 19, about 56.3 million people in the U.S. had received one or both doses of a COVID vaccine.
While the VAERS database numbers may seem sobering, according to a U.S. Department of Health and Human Services study, the actual number of adverse events is likely significantly higher. VAERS is a passive surveillance system that relies on the willingness of individuals to submit reports voluntarily.
According to the VAERS website, healthcare providers are required by law to report to VAERS:
The CDC says healthcare providers are strongly encouraged to report:
However, “within the specified time” means that reactions occurring outside that timeframe may not be reported, in addition to reactions suffered hours or days later by people who don’t report those reactions to their healthcare provider.
Vaccine manufacturers are required to report to VAERS “all adverse events that come to their attention.”
Historically, however, fewer than fewer than 1% of adverse events have ever been reported to VAERS, a system that Children’s Health Defense has previously referred to as an “abject failure,” including in a December 2020 letter to Dr. David Kessler, former FDA director and now co-chair of the COVID-19 Advisory Board and President Biden’s version of Operation Warp Speed.
A critic familiar with VAERS’ shortcomings bluntly condemned VAERS in The BMJ as “nothing more than window dressing, and a part of U.S. authorities’ systematic effort to reassure/deceive us about vaccine safety.”
CHD is calling for complete transparency. The children’s health organization is asking Kessler and the federal government to release all of the data from the clinical trials and suspend COVID-19 vaccine use in any group not adequately represented in the clinical trials, including the elderly, frail and anyone with comorbidities.
CHD is also asking for full transparency in post-marketing data that reports all health outcomes, including new diagnoses of autoimmune disorders, adverse events and deaths from COVID vaccines.
Children’s Health Defense asks anyone who has experienced an adverse reaction, to any vaccine, to file a report following these three steps.
What’s “incoherent” about it?
The headlines sound clear to me.
Did your dad yell at you?
actually, the deaths were within 48 and may have
been time correlated with the INJECTIONS of the
DNA operating systems (never tested over, say, 7 years).
and Tylenol has an ingredient which causes
hepatitis with contraction of the hepatic envelope
and seriously elevated bilirubin in some.
you certainly failed to read the urls sent in response
to your last BS.
Some deaths were within 48 hours. So what? What else did those people do in the 48 hours before they died? Sit in a chair? Read a book? Go for a walk? Does walking cause death because somebody went for a walk and then died within 48 hours?
Its both.
Two for the price of one. I know, it can strain the old noodle. If you ask nicely, I can explain what everything means.
Your “doctor” said no such thing, unless your “doctor” has a doctorate in underwater basket weaving.
YOU have no idea what AMPUs doc said.
Look...your shilling for admittedly FAKE numbers CDC/BigPharma is getting old. So is your calling everyone who simply wants a PROVEN, non-experimental vaccine....that is not just FDA approved under EUA, “anti-vaxxers”. THAT is what is not true.
Time will tell what these experimental agents will do, six months to several years down the road.
In the meantime...we get it....you cheer for the BigPharma team.
Stop with the name calling.
Why does it take on average around 10 years for a drug to be approved by the FDA? Why was this rushed out in under 8 months? Why even with 10 years of data do serious adverse and fatal events occur with drugs that were deemed safe?
“Data collected through February 18th from the v-safe pregnancy registry indicate that the reactogenicity profile and adverse events observed among pregnant individuals in v-safe did not indicate any safety concerns. Additionally, side effects were similar in pregnant and non-pregnant populations. Specific pregnancy outcome data for 275 completed pregnancies are included in Table 2. As demonstrated below, no differences have been seen when comparing pregnant women participating in the v-safe pregnancy registry with the background rates of adverse pregnancy outcomes.” - American College of Obstetricians and Gynecologists
But how do we wake up the sheep?
They are docile.
#SilenceOfTheLambs
What is truly amazing is how they’ve had to fake China Flu death numbers to justify their lockdowns and fake vaccines....and, people HERE, on this forum, mask up, lock up and get in line to be test subjects.
Just incredible.
“One week after receiving a covid vaccine I had a pulled muscle in my back.
Just after a day of yard work.
But I am sure it had nothing to do with the yard work.
I should have reported?”
**************************************************
Just a week after receiving the vaccine? That HAS TO BE more than coincidence. Report that vaccine adverse event to VAERS immediately.
You are a flaming fool to take and or claim something is safe WHERE THE MAKER STATES THE MAJORITY OF THOSE DRUGS FAIL TO BE CERTIFIED AFTER LONG TERM TRAILS ARE COMPLETED.
THE MAJORITY. LET THAT SINK IN.
Thalidomide was also considered safe and took 2-3 years to be pulled from the market.
Let me guess. You work for the CDC, don’t you? Anyone can look at the VAERS report and see direct cause and effect to the Covid vaccine.
Except the CDC. They are willfully blind and will not admit to the thousands of reported deaths due to various vaccines.
There is a spectrum of variation for most things.
I believe some folks have died from drinking too much water.
That is the most amazing thing of all and says there is little hope.
Sheep Bill could not be reached for comment. He already got his vax.
Speaking the language of truth for even stupid Q-tards.
“Where the stupid go, the stupidest go Q-tard.”
Disclaimer: Opinions posted on Free Republic are those of the individual posters and do not necessarily represent the opinion of Free Republic or its management. All materials posted herein are protected by copyright law and the exemption for fair use of copyrighted works.