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January 8, 2021 (LifeSiteNews) – The list of people who have visited the emergency room after receiving the COVID-19 vaccine is in the hundreds and those who have suffered adverse reactions are over 1,000, according to the Notification System. Vaccine Adverse Events (VAERS).
VAERS is a reporting system administered by the Centers for Disease Control and Prevention (CDC) and the Federal Drug Administration (FDA). It collects information from the public about adverse reactions to vaccines. The CDC and the FDA consider the data useful to detect any potential problems with vaccines licensed in the USA. According to its website, “Healthcare professionals are required to report certain adverse events and vaccine manufacturers are required to report any adverse events of which they are aware.
From the first days of the first injections administered, people began to experience things like “nausea, tremors, stitches and wheezing”.
“A healthcare professional at Bartlett Regional Hospital in Alaska, was suspected of having a severe allergic reaction, or anaphylaxis, after receiving the Pfizer vaccine. She was taken to the emergency room and spent several nights there before being discharged ”, reported The Epoch Times.
Since then, a second healthcare professional from the same hospital in Alaska has also suffered adverse side effects from the Pfizer-BioNTech COVID-19 vaccine. Doctors administered epinephrine to open his airways. A statement posted on the Juneau city website says: “A second member of the team had eye swelling, dizziness and itchy throat ten minutes after the injection.”
Yet another Alaskan woman, an employee of the Foundation Health Partners in Fairbanks, suffered an allergic reaction to the vaccine. This woman had “no known allergies, but had already experienced an adverse reaction to a bee sting. In a statement, the Foundation Health Partners said the employee was being monitored after receiving the vaccine when she started experiencing anaphylactic symptoms 10 minutes later, “reported WBTV.
“The system received reports of 1,156 adverse events in total. Of these, 17 were ‘fatal’ and two led to ‘permanent disability’ ”.
Thousands of others report an inability to return to work immediately or perform normal daily activities after the vaccine. According The Epoch Times, these incidents were reported through V-safe, “a smartphone app … that uses text messages and web searches to provide personalized health checks and allows users to quickly notify CDC if they are experiencing side effects” .
The FDA is reportedly investigating allergic reactions to the coronavirus vaccine Pfizer. He alerted the public.
“The current FDA guidance says that most Americans with allergies should be allowed to get the vaccine, but that people who have had severe reactions to other vaccines should not be vaccinated.” In addition, those who have had reactions to the vaccine should not receive a second dose.
On January 6, the number of notifications was “308 patients sent to emergency rooms in hospitals documented in the Vaccine Adverse Event Notification System (VAERS). This represents 0.0064 percent of the total vaccinations, 4.8 million. “
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Vaccine manufacturers cannot be prosecuted if their products injure or kill someone, thanks to a federal law in the 1980s that requires such cases to be dealt with through the secret National Vaccine Injury Compensation Program. This program was widely criticized by vaccine security watchers as inappropriate and manipulated against complainants.