UK Adverse Events ‘Yellow Card’ Reports UPDATED AS OF FEB. 21:
NUMBER OF DEATHS REPORTED: 460
NUMBER OF REPORTS FILED: 72,920
TOTAL NUMBER OF ADVERSE REACTIONS REPORTED: 243,050
Note: The UK only counts deaths within 1 week of vaccination.
EVIDENCE OF COVID-19 VACCINE INJURIES & DEATHS
This document is intended to provide some insight into and evidence of possible adverse reactions to COVID-19 vaccines. It is structured as follows:
- A background on harms caused by other vaccines, which were only discovered after they were licensed and marketed. This includes at least 2 examples where the vaccine was suspended due to a relatively small number of reports of injury or death. This section includes links to supporting documentation from
mainstream sources, published research and the CDC.
What we will see is that at least 2 vaccines were suspended due to a relatively small number of reported adverse events, with thorough investigations only being launched afterwards. In other words, historical precedent shows that the CDC takes reports very seriously and in at least 2 cases suspended a vaccine based on a small number of reports. Why are they not doing that now when a large number of serious adverse events are being reported?
- A discussion of the Vaccine Adverse Events Reporting System (VAERS) and summary of studies that have tried to measure the extent to which adverse events are underreported.
- A presentation and discussion of data on adverse events reported to VAERS for COVID-19 vaccines, including deaths.
- Presentation of adverse events based on EU, UK and Israeli data and links to news reports on 4 adverse events: anaphylaxis, Bell’s palsy, autoimmune thrombocytopenia and vaginal bleeding.
- A compilation of news and social media reports detailing anecdotes of many adverse events of people shortly after receiving a COVID-19 vaccine. Here is another compilation. I don’t think all of these are real, but I don’t think all of them are fake.
- A discussion of possible mechanisms by which COVID-19 vaccines could cause adverse reactions.
PREVIOUS PROBLEMS W/LICENSED VACCINES
Many people believe that since the short term safety studies involving tens of thousands of participants did not show severe adverse reactions, then the unlicensed but authorized for emergency use vaccines for COVID-19 must be safe. But many licensed vaccines that went through clinical trials have been found to cause injury and even been recalled after the fact. Some examples are below.
Keep in mind that most of the information presented below comes from mainstream sources, which we can expect to underestimate the harm caused by vaccines. In fact, there is an argument to be made that every vaccine produces harm even though the damage may only manifest years later and appear unconnected to the vaccine. Also, calling these gene therapy injections “vaccines” is just a way to take advantage of the indemnity extended to vaccines so the manufacturers can’t be sued. Remember that all of the chronic and auto-immune diseases wreaking havoc on us and fueling the trillion-dollar pharmaceutical industry can be found among the “side effects” of the inserts packaged with every vaccine. It’s a classic racket: profiting off of problems you create. (If you want to share this document with friends or family but believe this statement is too radical for them, here is a link to a slightly more palatable version.)
- The Dengue Virus developed by Sanofi Pasteur and introduced in the Philippines. According to Wikipedia, “The program was stopped when Sanofi Pasteur advised the government that the vaccine could put previously uninfected people at a somewhat higher risk of a severe case of dengue fever…. In late November 2017, the DOH suspended the school-based vaccination program.” The Philippine Department of Justice filed criminal charges against health and regulatory officials and officials of Sanofi Pasteur for “reckless imprudence resulting in homicide,” alleging that the vaccine was marketed despite awareness of its risks. More on this at NPR.
- The vaccine approved for use against the 2009 H1N1 “swine flu” epidemic caused narcolepsy or cataplexy in about 1 in 16,000 people,
with more than 800 children “so far known to have been made ill by the vaccine.” As that link shows, the UK government paid out 60 million pounds to people in the UK afflicted. More from that link:
“There’s no doubt in my mind whatsoever that Pandemrix increased the occurrence of narcolepsy onset in children in some countries – and probably in most countries,” Emmanuelle Mignot, a specialist in sleep disorder at Stanford University in the United States told Reuters.”
“Among [those affected] is Josh Hadfield, 8, from Somerset, who is on anti-narcolepsy drugs costing £15,000 a year to help him stay awake during the school day.”
“‘If you make him laugh, he collapses. His memory is shot. There is no cure. He says he wishes he hadn’t been born. I feel incredibly guilty about letting him have the vaccine,’ said his mother.”
“Despite a 2011 warning from the European Medicines Agency against using the vaccine on those under 20 and a study indicating a 13-fold heightened risk of narcolepsy in vaccinated children, GSK has refused to acknowledge a link.”
- Until at least 1963, the polio vaccine was contaminated, exposing at least 98 million people to a highly carcinogenic monkey virus, SV-40. People vaccinated against polio thought to be contaminated show an increased risk of many different cancers.
- The first vaccine against Rotavirus was approved for use in 1998, but withdrawn a year later after it was found that babies who received the vaccine were at greater risk of developing intussusception, a type of bowel blockage that can be fatal if not addressed in time. The vaccine became available in October 1998 and in July 1999, the CDC suspended the vaccine after just 15 cases of intussusception had been reported to VAERS (see below).
- The 1976 Swine Flu vaccination campaign was stopped after 25 deaths and 362 cases were reported of people developing Guillain Barré syndrome following vaccination.
- The Canadian government withdrew the Trivirix MMR vaccine in 1987 “because of an association between the Urabe Am9 [mumps] strain and aseptic meningitis.” That vaccine was then licensed under a different name and introduced to the U.K. in 1988, even though regulators were aware of widespread reports of cases of meningitis from the vaccine. The vaccine was withdrawn from the UK market in 1992 following the leak of early results of a study showing a higher risk of meningitis among children who received that vaccine.
- The Cutter Incident: “On April 12, 1955, following the announcement of the success of the polio vaccine trial, Cutter Laboratories became one of several companies that was recommended to be given a license by the United States government to produce Salk’s polio vaccine…. some lots of the Cutter vaccine—despite passing required safety tests—contained live polio virus in what was supposed to be an inactivated-virus vaccine…. The mistake produced 120,000 doses of polio vaccine that contained live polio virus. Of children who received the vaccine, 40,000 developed abortive poliomyelitis (a form of the disease that does not involve the central nervous system), 56 developed paralytic poliomyelitis—and of these, five children died from polio. The exposures led to an epidemic of polio in the families and communities of the affected children, resulting in a further 113 people paralyzed and 5 deaths…. After a thorough investigation, they found nothing wrong with Cutter’s production methods. A congressional hearing in June 1955 concluded that the problem was primarily the lack of scrutiny from the NIH Laboratory of Biologics Control…. All five companies that produced the Salk vaccine in 1955…had difficulty completely inactivating the polio virus. Three companies other than Cutter were sued, but the cases settled out of court. The NIH Laboratory of Biologics Control, which had certified the Cutter polio vaccine, had received advance warnings of
problems: in 1954, staff member Dr. Bernice Eddy had reported to her superiors that some inoculated monkeys had become paralyzed and provided photographs.”
- The Bill & Melinda Gates Foundation is by far the biggest promoter of vaccines in the world. The Indian government’s vaccination board recently cut financial ties with the foundation following a report showing the financial conflicts of interest and accusing the foundation of “altering aid priorities by ‘legitimizing the role of multinational pharmaceutical companies’ by pushing for public private-partnerships (PPPs). According to Global Justice Now, both the BMGF-funded Global Fund to Fight AIDS, Tuberculosis and Malaria (GFATM) and the GAVI Alliance, are PPPs and have questionable associations with the pharmaceutical industry.”
In 2010, an HPV vaccination trial run by the BMGF- PATH NGO was halted early over safety concerns and the use of unethical procedures, and a parliamentary committee “excoriated U.S. nonprofit [running the trials] and its Indian partner for alleged ethical violations in a trial of a vaccine to protect against cervical cancer caused by the human papillomavirus (HPV)” and recommended legal action against the organization running the trials. “Rather than endeavoring to protect women’s health, PATH, [the committee] charged, was a willing tool of foreign drug companies hoping to convince the Indian government to include the HPV vaccine in its universal vaccine program, a roster of mandatory immunizations that the government is required to pay for. ICMR [an Indian regulatory agency], the panel’s report asserts, has “completely failed to perform [its] mandated role and responsibility as the apex body for medical research in the country. … Rather, in [its] over-enthusiasm to act as a willing facilitator of the machinations of PATH, [it has] even transgressed into the domain of other agencies which deserves the strongest condemnation and strictest action against [it].”
“In 2014, doctors from the Kenyan Catholic Doctors Association discovered that the tetanus vaccinations that had been administered to 2.3 million girls and women by the World Health Organization and UNICEF [which are heavily funded by the BMGF] had been contaminated with the anti-fertility hormone hCG.” This was not the first time that WHO was found distributing hCG-laced tetanus vaccines. Tetanus vaccines combined with hCG were developed by WHO researchers in the 1970’s as a “birth control vaccine.”
The Corvelva NGO in Italy hired a scientist to conduct an analysis of the contents of several vaccines marketed in Italy and found many surprising results, including insufficient levels of antigens, large amounts of human and animal DNA, and many other strange things.
What Is VAERS and How Reliable Is It?
One of the ways we learn about adverse events from approved vaccines is the CDC’s Vaccine Adverse Event Reporting System (VAERS). From the VAERS website:
“VAERS is a national early warning system to detect possible safety problems in U.S. licensed vaccines… VAERS accepts and analyzes reports of adverse events (possible side effects) following vaccination….
“VAERS is not designed to detect if a vaccine caused an adverse event, but it can identify unusual or unexpected patterns of reporting that might indicate possible safety problems requiring a closer look.”
It was created by the 1986 National Childhood Vaccine Injury Act that limited vaccine manufacturer liability for vaccine injury and created a national system of vaccine injury compensation, which has paid out about $4.5 billion since its creation.
Because it is passive (reports are made voluntarily) and most people are unaware it exists, adverse events following vaccination are underreported. The rate of underreporting is currently unknown, but based on available evidence it is very high:
- This meta-analysis of research on underreporting of adverse events from pharmaceutical drugs (not vaccines) found the median rate of underreporting overall to be 94% and 80% for serious adverse reactions. A paper by former FDA commissioner David Kessler cites a study showing that only 1% of serious adverse events from drugs are reported. Adverse reactions to vaccines are arguably even less likely to be reported because people are less likely to acknowledge or connect adverse events from vaccinations than they are from a drug.
- An HMO in New England was awarded a million-dollar grant from the AHRQ to automate the process of reporting to VAERS. In their grant report, they state: “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.” (No citation is given so source of statement is unclear; possibly from internal testing.) This would mean that only 1 out of 100 or fewer adverse events are reported.
They never had a chance to test the system they developed against VAERS, because “the necessary CDC contacts were no longer available and the CDC consultants responsible for receiving data were no longer responsive to our multiple requests to proceed with testing and evaluation.”
- Another study of a partially automated reporting system in a large healthcare network found the odds of a physician submitting a report after the new system was implemented was 30-times higher than prior to implementation.
- A CDC study of VAERS underreporting for two serious adverse events, anaphylaxis and Guillain-Barré syndrome (GBS), estimated a range of underreporting depending on the event and the vaccine. For anaphylaxis they estimated between 13-25% of adverse events were reported for most vaccines except the H1N1 vaccine in 2009 where 76% of events were reported. For GBS, VAERS was estimated to capture between 12% to 64% of events.
COVID-19 Vaccine Reports to VAERS
So even though VAERS cannot be used to conclude a causal relationship between vaccination and an adverse event, it is used by the CDC to monitor vaccines for safety “signals.” What kinds of signals are being reported to VAERS?
As of Feb. 26, there have been 1,265 deaths reported to VAERS following a COVID vaccine. If the estimates above based on attempts to automate vaccine adverse event reporting are correct, the true number of deaths is somewhere between 30 to 100 times that number, or between 37,950 deaths and 126,500 deaths. If the CDC study on anaphylaxis and GBS applies, reported deaths should be between 1,664 and 9,730.
Total adverse events reported for COVID-19 vaccines: 32,409 Total number if 30x underreporting: 972,270
Total number if 99x underreporting: 3,240,900
Adverse events listed as SERIOUS: 8,911
Total number if 30x underreporting: 267,330
Total number if 99x underreporting: 891,199
Adverse events listed as REQUIRING HOSPITALIZATION: 2,743 Total number if 30x underreporting: 82,290
Total number if 99x underreporting: 274,300
Adverse events categorized as ‘PERMANENT DISABILITY’: 479 Total number if 30x underreporting: 14,370
Total number if 99x underreporting: 47,900
17% OF DEATHS ON SAME DAY AS VACCINATION 47% WITHIN 2 DAYS OF VACCINATION
Reported deaths by days since COVID-19 vaccination (VAERS as of 2/26): According to this news article, the death rate per vaccine dose is much higher than the flu vaccine this year:
“According to the federal Vaccine Adverse Event Reporting System (VAERS), there were 21 deaths this flu season after 180+ million flu vaccines, a rate of 1 death per 9,000,000 vaccinations.”
“The COVID-19 vaccine, however, according to VAERS, shows 1 death reported per 35,000 shots or 10,000 completed vaccinations (so far), a 300-900 greater likelihood. The Center for Disease Control (CDC) maintains there is “no link” between the vaccine and the deaths.”
- If VAERS is supposed to provide the CDC with a signal about potential problems with (new) vaccines, why are they dismissing these deaths rather than launching some kind of investigation into this signal?
- The 1976 Swine Flu and the 1998 Rotavirus vaccines were suspended based on far fewer reports of adverse events. The CDC is ignoring historical precedent. Why? And why has it not suspended the COVID-19 vaccines based on the much larger number of reported adverse events and deaths?
Actually, the Israeli Ministry of Health just announced an investigation into reports of inflammation of the meninges and the heart muscle (including pericarditis and myocarditis) in people shortly following vaccination. (It is worth noting that 20% of VAERS reports for COVID-19 vaccines were cardiac-related.) But these are only a fraction of reported events. The investigation needs to be expanded to include ALL morbidity and mortality.
The Israeli government could easily do this, because their health records are highly centralized, and they know whether and when people were vaccinated and if they had any documented health problems after. They already used the data to publish a (flawed) study of the vaccines’ effectiveness. If they wanted to put this
issue to rest, they could, but as of this writing they have not. Why not?
Each VAERS case is assigned a unique ID number and has a description of the incident (death, disability, etc.)
On the following pages are approx. 70 of the 929 deaths recorded in VAERs. Anyone can view the database via the following steps:
- Accept the disclaimer at bottom of page
- Click on VAERS data search
- In section 1, click on group results by “VAERS ID” , and by “vaccine type” and by “event category” 4. Under optional measures (still in section 1) tick off “adverse event description”
- Scroll down to section 3 and under Vaccine Products select “Covid19 vaccine” Make sure it is the only option selected. (You will have to deselect “All vaccine products” from the top of the list.)
- Scroll down to section 5 and under event category select “death”. Make sure it is the only option selected. (Don’t forget to deselect “all events” from the top of the list).
Scroll to the very bottom and click send.
VAERS ID # 938118-1 AGE 51. FEMALE Vaccinated 1/5/2021. Died. 1/10/2021. Pfizer vaccine. On 1/8/2021 17:30 patient taken to ER, cerebellar hemorrhage, stroke, aneurysm.
VAERS ID # 946293-1 AGE 51. MALE Vaccinated 1/7/2021. Moderna . Became increasingly hypoxic around 1800hours on 1/7/2021. Transported to ER for acute on chronic hypoxia respiratory failure. Expired on 1/12/[email protected] at med center.
VAERS ID # 918518-1 AGE 50. FEMALE Vaccinated 12/31/2020. Died 12/31/2020. Moderna
VAERS ID # 930910-1 AGE 52. FEMALE Vaccinated 1/8/2021. Died 1/8/2021. Patient received COVID vaccination 12:15pm. Patient was monitored for the appropriate amount of time by nursing staff. Patient passed away at 2:15pm. Moderna
VAERS ID # 933739-1 AGE 54. FEMALE. Vaccinated 1/8/2021. Died 1/10/2021. 2 days later. Staff member checked on her at 3am and patient stated that she felt like she couldn’t breathe. 911 was called and taken to the hospital. While in the ambulance, patient coded. Two EEGs were given to determine that patient had no brain activity. Pfizer
VAERS ID # 923219-1 AGE 41. FEMALE Vaccinated 12/30/2021. Died. 1/1/2021. Pfizer vaccine. The patient did not experience any adverse event at the moment of inoculation with COVID-19 vaccine or the following days. On January 1, 2021, at lunch time, two days after receiving the vaccine, the patient was found unresponsive in her bed by her partner.
VAERS ID # 936805-1 AGE 25. MALE Vaccinated 12/22/2020. Found unresponsive and expired at home on 1/11. Moderna
VAERS ID # 943397-1 AGE 28. MALE Vaccinated 12/23/2020. Died 1/14/2021. Patient was found unresponsive at work in the hospital. Patient pupils were fixed and dilated. Pfizer
VAERS ID # 939050-1 AGE 32. FEMALE Vaccinated 12/28/2020. Died on 1/4/21 at 7:20am. Moderna
VAERS ID # 921667-1 AGE 39. FEMALE Vaccinated 12/29/2020. It was reported that the staff member deceased somewhere between 1/3/2021 and 1/4/2021. Pfizer
VAERS ID # 933578-1 AGE 43. MALE Vaccinated 1/8/2021. Died 1/9/2021. Moderna
VAERS ID # 937527-1 AGE 44. FEMALE Vaccinated 12/23/2020. Died on 1/4/2021. Pfizer
VAERS ID # 929764-1AGE 45. MALE Vaccinated 12/28/2020. Died 12/29/2020. The patient was found deceased at home about 24 hours after immunization. Moderna
VAERS ID # 934968-1AGE 54. MALE Vaccinated 1/4/2021. Died 1/6/2021. Pfizer. The patient received the vaccine on 04Jan2021, after which he started not feeling well. He went right home and went to bed. He woke up and ate a bit but not much and then was kind of pale. The patient then started to vomit, which continued throughout the night. He was having trouble in breathing. Emergency services were called, and they took his vitals and said that everything was okay, but he was very agitated; reported as not like this prior to the vaccine. The patient was taken to urgent care where they gave him an unspecified steroid shot and unspecified medication for vomiting. The patient continued to vomit throughout the day and then he was very agitated again and would fall asleep for may be 15-20 minutes. When the patient woke up, he was very restless (reported as: his body was just amped up and could not calm down). The patient calmed down just a little bit in the evening. When the patient was awoken at 6:00 AM in the morning, he was still agitated. The patient stated that he couldn’t breathe, and his mind was racing. The patient’s other brother went to him and he was not responsive, passed on 06Jan2021 around 10:15 AM. It was reported that none of the symptoms occurred until the patient received the vaccine.
VAERS ID # 942106-1 AGE 54. MALE Vaccinated 1/8/2021. Died 1/9/2021. Pfizer vaccine. On scene, the patient had a witnessed arrest with EMS starting CPR. He was given 3 rounds of epi without ROSC. Patient's wife, had noted patient had received covid vaccine the prior day.
VAERS ID: 924456-1, AGE 85 vaccination was administered at approx. 10:00 AM and the patient continued throughout day without any complaints or signs of adverse reaction. When the nursing staff went to the room to check on the resident patient was found unresponsive, no chest rises, noted regurgitated small amount of food to mouth left side.
VAERS ID # 928933-1 AGE 56. FEMALE Vaccinated on 12/23/2020. Died on 1/8/2021. Moderna.
VAERS ID # 935511-1 AGE 56. FEMALE Vaccinated 1/8/2021. Died 1/9/2021. Moderna. Patient received the 1st dose of Moderna and was found deceased in her home the next day.
VAERS ID # 941811-1 AGE 56. FEMALE Vaccinated 1/4/2021. Died 1/11/2021. Moderna. Resident began having fever on 1/11/21. Resident sent to nearest ER for evaluation. Later in the evening the staff AT Medical Center called to inform staff that resident had expired @ 2230 as a result of Respiratory Failure and Sepsis.
VAERS ID # 944595-1 AGE 56. MALE Vaccinated 1/12/2021. Died 1/14/2021. Pfizer. Cardiac arrest within 1 hour Patient had the second vaccine approximately 2 pm on Tuesday Jan 12th He works at the extended care community and was in good health that morning with no complaints. He waited 10-15 minutes at the vaccine admin site and then told them he felt fine and was ready to get back to work. He then was found unresponsive at 3 pm within an hour of the 2nd vaccine. EMS called immediately worked on him 30 minutes in field then 30 minutes at ER was able to put him on life support yet deemed Brain dead on 1-14-21 and pronounced dead an hour or so later.
VAERS ID # 921768-1 AGE 58. FEMALE Vaccinated 1/4/2021. Died 1/4/2021. Pfizer.
VAERS ID # 920815-1 AGE 58. FEMALE Vaccinated 12/30/2020. Died 1/4/2021. 6 days later. Moderna . VAERS ID # 930154-1 AGE 60. MALE Vaccinated 1/5/2021. Died 1/8/2021. Moderna.
VAERS ID # 933090-1 AGE 60. MALE Vaccinated 1/5/2021. Died. 1/9/2021. Pfizer.
VAERS ID # 939270-1AGE 48. MALE Vaccinated 12/22/2020. Died 12/31/2020. Pfizer
VAERS ID # 941743-1 AGE 60. FEMALE Vaccinated 1/12/2021. Died 1/13/2021. Moderna. Found deceased at 3am
VAERS ID # 932898-1 AGE 61. MALE Vaccinated 12/17/2020. Died. 12/30/2020. Pfizer vaccine. The patient had an apparent cardiac arrest on 12/23/20 and was admitted to the ICU. He was taken off of life support on 12/30/20.
VAERS ID # 942085-1 AGE 62. FEMALE Vaccinated 1/2/2021. Died 1/8/2021. Pfizer. On 1/8/21 at 0615 resident was shaking. Reported all over pain. At 0850 she was not responsive.
VAERS ID # 940955-1 AGE 66. FEMALE. Vaccinated 1/11/2021. Died 1/11/2021. Pfizer. Cardiac Arrest. Patient was found pulseless and breathless 20 minutes following the vaccine administration. Received the second dose of BNT162B2. Took the first dose on 21Dec2020. MD found no signs of anaphylaxis.
VAERS ID: 926600-1, 65yo Patient did not report any signs or symptoms of adverse reaction to vaccine. Patient reported not feeling well and passed away that day.
VAERS ID: 925154-1, 84yo DEATH within 1 day, no current illness.
VAERS ID: 926797-1, 93yo had a vaccination on 12/31/2020 late morning passed away early morning 01/01/2020.
VAERS ID: 927189-1, 74yo Patient was vaccinated at 11am and was found at the facility in his room deceased at approximately 3:00pm. Nurse did not have cause of death
VAERS ID: 927260-1, 87yo No adverse effects noted after vaccination. Patient found unresponsive at 16:45 on 1/6/21. Abnormal breathing patterns, eyes partially closed SPO2 was 41%, pulseless with no cardiac sounds upon auscultation. CPR, pulse regained, patient breathing. Patient sent to ER had multiple cardiac arrest and severe bradycardia and passed.
VAERS ID: 924664-1, 92yo No current illness. At 1855, I was alerted by caregiver, resident was not responding. Per caregiver, she was doing rounds and found resident in bed, unresponsive, mouth open, observed gurgling noises. Primary caregiver observed resident at baseline and ambulating after dinner at approximately, 1800 less than an hour prior to incident. Resident received the first dose of vaccine on 1/2. Expired at 0615 per Castle RN.
VAERS ID: 923993-1, 62yo Patient was vaccinated Dec 30, 2020. Prime dose of Moderna vaccine. Observed for full 15 minutes post-injection. No complaints when asked during observation. Released. Subsequently, vaccine clinic staff learned from the patient’s supervisor that patient had expired on Jan 2, 2021at his home.
VAERS ID: 909095-1, 66yo on 12/24/2020 the resident was sleepy and stayed in bed most of the shift. He stated he was doing okay but requested pain medication for his legs at 250PM. At 255AM on 12/25/2020 the resident was observed in bed lying still, pale, eyes half open and foam coming from mouth and unresponsive. He was not breathing and with no pulse.
VAERS ID: 924464-1, 61yo coughing up blood, significant hemoptysis — > cardiac arrest. started day after vaccine
VAERS ID: 921768-1, 58yo Vaccine received at about 0900 on 01/04/2021 at her place of work, Medical Center, where she was employed as a housekeeper. About one hour after receiving the vaccine she experienced a hot flash, nausea, and feeling like she was going to pass out after she had bent down. Later at about 1500 hours she appeared tired and lethargic, then a short time later, at about 1600 hours, upon arrival to a friends home she complained of feeling hot and having difficulty breathing. She collapsed, when medics arrived, she was still breathing slowly then went into cardiac arrest and was unable to be revived.
VAERS ID: 910363-1, 84yo Patient had mild hypotension, decreased oral intake, somnolence starting 3 days after vaccination and death 5 days after administration.
VAERS ID: 913143-1, 84yo Vaccine administered with no immediate adverse reaction at 11:29am. Vaccine screening questions were completed and resident was not feeling sick and temperature was 98F. At approximately 1:30pm the resident passed away.
VAERS ID: 913733-1, 85yo My grandmother died a few hours after receiving the moderna covid vaccine booster 1. The treating hospital did not acknowledge this and I wanted to be sure a report was made.
VAERS ID: 914604-1, 74yo Spouse awoke 12/20 and found spouse dead. Client was not transferred to hospital.
VAERS ID: 914690-1, 83yo Within 24 hours of receiving the vaccine, fever and respiratory distress, and anxiety developed requiring oxygen, morphine and ativan. My Mom passed away on the evening of 12/26/2020.
VAERS ID: 914805-1, 63yo RESIDENT CODED AND EXPIRED
VAERS ID: 914895-1, 78yo Injection given on 12/28/20 – no adverse events and no issues yesterday; Death today, 12/30/20, VAERS ID: 914917-1, 63yo Death by massive heart attack. Pfizer-BioNTech COVID-19 Vaccine EUA VAERS ID: 914961-1, 88yo pt passed away with an hour to hour and 1/2 of receiving vaccine.
VAERS ID: 914994-1, 90yo pt was a nursing home pt. pt received first dose of covid vaccine. pt was monitored for 15 minutes after getting shot. staff reported that pt was 15 days post covid. Pt passed away with in 90 minutes of getting vaccine.
VAERS ID: 915562-1, 88yo pt received vaccine at covid clinic on 12/30 at approximately 3:30, pt vomited 4 minutes after receiving shot–dark brown vomit, Per staff report pt became short of breath between 6 and 7 pm that night. Pt passed away at approximately 10pm.
VAERS ID: 915682-1, 85yo Resident received vaccine per pharmacy at the facility at 5 pm. Approximately 6:45 resident found unresponsive and EMS contacted. Upon EMS arrival at facility, resident went into cardiac arrest, code initiated by EMS and transported to hospital. Resident expired at hospital at approximately 8 pm
VAERS ID: 915920-1, 96yo Resident was living in an assisted living facility. She fell on 11/24/2020 and was admitted to this facility for rehab. Received vaccine 12/28/2020 in am and expired that afternoon.
VAERS ID: 918065-1, 64yo Vaccine 12/30/2020. 1/1/2020: Pronounced deceased 1/1/2020
VAERS ID: 918388-1, 65yo Vaccine 12/30/2020. 1/1/2020: Resident found unresponsive without pulse, respirations at 04:30 CPR performed, expired at 04:52 by Rescue, No acute illness at time of vaccination.
VAERS ID: 918418-1, 65yo Vaccine 12/30/2020. 1/1/2020: Resident became SOB, congested and hypoxic requiring oxygen, respiratory treatments and suctioning. Stabilized after treatment and for the next 72 hours with oxygen saturations in the 90s. On 1/3/2021 was found without pulse and respirations.
VAERS ID: 918487-1, 94yo Two days post vaccine patient went into cardiac arrest and passed away. VAERS ID: 915880-1, 99yo Patient died within 12 hours of receiving the vaccine.
VAERS ID: 918518-1, 50yo syncopal episode – arrested – CPR – death
VAERS ID: 919108-1, 100yo Fever, Malaise, passed the day after vaccine.
VAERS ID: 919537-1, 96yo Resident exhibited no adverse events during 30 minute monitoring following vaccine administration. Resident found without pulse at 1900.
VAERS ID: 920326-1, 89yo Redness and warmth with edema to right side of neck and under chin. Resident expired on 1.1.21.
VAERS ID: 920545-1, 93yo “The resident received is vaccine around 11:00 am and tolerated it without any difficulty or immediate adverse effects. He was at therapy from 12:36 pm until 1:22 pm when he stated he was too tired and could not do anymore. The therapist took him back to his room at that time and he got into bed himself but stated his legs felt heavy. At 1:50 pm the CNA answered his call light and found he had taken himself to the bathroom. She stated that when he went to get back into the bed it was “”abnormal”” how he was getting into it so she assisted him. At that time he quit breathing and she called a RN into the room immediately. He was found without a pulse, respirations, or blood pressure at 1:54 pm.
VAERS ID: 920815-1, 58yo Found deceased in her home, unknown cause, 6 days after vaccine.
VAERS ID: 920832-1, 104yo Vaccine 12/30/2020 Screening PCR done 12/31/2020 Symptoms 1/1/2021 COVID test result came back positive 1/2/2021 Deceased 1/4/2021
VAERS ID: 921175-1, 77yo Resident received Covid Vaccine, noted after 30 mins with labored breathing BP 161/77, HR 116, R 38, T 101.4,epipen administered, sent to ER, died
VAERS ID: 921481-1, 88yo Vaccine given on 12/29/20 by Pharmacy. On 1/1/21, resident became lethargic and sluggish and developed a rash on forearms. Resident expired on 1/4/2021
VAERS ID: 921547-1, 65yo RESIDENT RECIEVED VACCINE ON 1/2/20. DEATH ON 1/4/2021.
VAERS ID: 921572-1, 87yo Resident had body aches, a low O2 sat and had chills starting on 12/30/20. He had stated that they had slightly improved. On 1/2/21 during the NOC shift his O2 sat dropped again. He later went unresponsive and passed away.
VAERS ID: 921667-1, 39yo LTCF Pfizer Vaccine clinic conducted 12/29/2020 Vaccine lead received a call indicating that a staff member deceased somewhere between 1/3/2021 and 1/4/2021. Cause of death is unknown, and an autopsy is being performed.
VAERS ID: 921880-1, 96yo The resident was found deceased a little less than 12 hours following COVID vaccination.
Article on VAERS Reports from Earlier Data Release (Feb. 14)
FDA has had 10
months to get a
system in place, but
is nowhere near
UK Adverse Events ‘Yellow Card’ Reports UPDATED AS OF FEB. 21:
NUMBER OF DEATHS REPORTED: 460
NUMBER OF REPORTS FILED: 72,920
TOTAL NUMBER OF ADVERSE REACTIONS REPORTED: 243,050
Note: The UK only counts deaths within 1 week of vaccination. More detailed data can be found at the link above (scroll down to Vaccine Analysis Profile links).
Summary of UK Data as of Jan. 24:
Article on UK Data up to Dec. 31, 2020
Click this link for the original source of this article.
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