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The U.S. Centers for Disease Control and Prevention (CDC) has confirmed an increase in the number of reported deaths following COVID-19 vaccination. Between December 14, 2020 and July 19, 2021, the Vaccine Adverse Event Reporting System (VAERS) received 12,313 reports of deaths among people who received a COVID-19 vaccine.
UPDATE: At 2:30 p.m. CT on July 21, 2021, the CDC website changed the number of VARS reports related to COVID-19 vaccine deaths from 12,313 to 6,079, through July 13, 2021. The last update date for the CDC webpage remains July 19, 2021.
UPDATE # 2: As of 6:30 p.m. CT on July 21, 2021, according to the CDC website until July 19, 2021, VAERS had received 6,207 death reports (0.0018%) among people who received a COVID-19 vaccine. The last update date of the CDC webpage reflects July 21, 2021.
Given that more than 338 million doses of COVID-19 vaccines have been administered in the United States, this data reflects a vaccination-to-mortality ratio of 0.0018%.
The CDC’s website states, “Reports of adverse events to VAERS after vaccination, including deaths, do not necessarily mean that a vaccine has caused a health problem. This is because the United States FDA requires healthcare providers to report any deaths after a COVID-19 vaccination to VAERS, even though it is not clear whether the vaccine was the cause.
Additionally, a review of available clinical information, including death certificates, autopsy, and medical records, has not established a causal relationship with COVID-19 vaccines, according to the CDC.
Additionally, VAERS had received 1,148 reports of myocarditis or pericarditis in people 30 years of age and under who received a COVID-19 vaccine as of July 19. The CDC and its partners are investigating these reports to assess whether there is a link to the COVID-19 vaccination.
Through follow-up, including review of medical records, the CDC and the Food and Drug Administration (FDA) confirmed 674 cases of myocarditis or pericarditis. In either case, the body’s immune system causes inflammation in response to an infection or some other trigger.
Most of these cases of heart inflammation have been reported to the CDC after vaccination with COVID-19 mRNA (Comirnaty or SpikeVax), especially in adolescents and young adults.
VAERS is the United States’ early warning system that monitors the safety of vaccines after they are cleared or licensed for use by the US FDA.
As of July 21, 2021, the FDA had issued three emergency use authorizations for COVID-19 vaccines. However, these experimental vaccines have not been approved by the FDA.
VAERS is part of the larger vaccine safety system, co-managed by the CDC and the FDA. VAERS accepts and analyzes reports of possible health problems – also known as “adverse events” – after vaccination.
As an early warning system, VAERS cannot prove that a vaccine caused a problem, the CDC says.
Specifically, a report to VAERS does not mean that a vaccine caused an adverse event. But VAERS can provide important information to the CDC and the FDA. If it appears that a vaccine may be causing a problem, the FDA and CDC will investigate further and take action if necessary.
In addition, anyone can submit a report to VAERS. Most VAERS reports are filed by healthcare professionals, vaccine manufacturers, and the general public. VAERS accepts all reports, regardless of the severity or likelihood that the vaccine caused the adverse event.
The United Kingdom (UK) healthcare system has a similar strategy.
As of July 7, 2021, the UK Medicines and Health Products Regulatory Agency (MHRA) had received 456 yellow card reports of suspected adverse reactions to the Pfizer-BioNTech vaccine (Comirnaty) in which the patient died shortly after time after vaccination, 983 reports for the COVID-19 AstraZeneca vaccine (Vaxzevria) and 7 for the COVID-19 Moderna vaccine (SpikeVax).
The majority of those yellow card reports were of older people or people with underlying illnesses, according to the UK’s MHRA.
PrecisionVaccinations publishes research-based and verified vaccine information.
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