CDC Releases Hidden COVID-19 Vaccine Injury Reports


Agency forced to disclose reports by federal judge.

The U.S. Centers for Disease Control and Prevention (CDC) has released previously hidden reports of facial paralysis and other adverse events following COVID-19 vaccination.

The 780,000 reports were received shortly after the COVID-19 vaccines were rolled out, and show people shared a wide range of postvaccination problems, including heart inflammation, miscarriages, and seizures.

“Loss of consciousness and seizure immediately following injection. Went to ER by ambulance,” one person reported.

“Diagnosed with Bells Palsy today due to left-sided facial numbness and paralysis,” another said.

People lodged the reports with V-safe, a new text-message system created by the CDC to monitor for possible side effects of COVID-19 vaccines.

The CDC for years declined to make the V-safe data public, instead publishing studies describing the reports as providing reassurance about the safety of the shots. However, according to data released in 2022, nearly 8 percent of the 10 million users required medical attention or hospital care after vaccination, and many others said they missed school, work, or other normal activities.

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That topline data came from check-the-box surveys.

The same judge that forced the release of that data ordered the agency in January to disclose free-text entries from a different area in which people could describe what happened to them. U.S. District Judge Matthew Kacsmaryk, an appointee of former President Donald Trump, rejected government arguments that it would take too much work to go through the responses and redact sensitive information.
The first two tranches, comprising 780,000 reports from some 523,000 people, include dozens of reports of heart inflammation, hundreds of reports of facial paralysis, and thousands of reports of tinnitus.

Multiple people said things were so bad that they were struggling with suicidal thoughts.

“For 24 hrs after shot I was so fatigued I could not stay awake. I also have some very strong suicidal thoughts. Zero appetite,” one individual wrote.

Another person said they experienced symptoms of an allergic reaction. “I read where this vaccine should not be administered to anyone allergic to PEG and I am allergic to PEG. It would be incredibly reassuring if someone would call me as all I run into is dead ends,” the individual said.

The free-text portion of the surveys was the only place for people to report many adverse events, including heart inflammation, even though the CDC knew the shots might cause those events, previously released documents showed. Other documents showed the CDC became aware of the vaccines possibly causing myocarditis, or heart inflammation, and a related condition called pericarditis early in 2021 but hid the knowledge from the public.

Judge Kacsmaryk’s order came in litigation brought by the Informed Consent Action Network (ICAN), a nonprofit that has compelled the release of a number of government files since the COVID-19 pandemic started.

“ICAN had to sue the Centers for Disease Control in order to gain access to the COVID-19 shot V-safe adverse event data, which is yet another shameful chapter in the decades-long history of federal health officials trying to cover up vaccine risks by ignoring patterns of vaccine reaction symptoms in reports made to the government,” Barbara Loe Fisher, co-founder and president of the National Vaccine Information Center, told The Epoch Times after reviewing the new data.

“When people report the same symptoms over and over again after getting a biological product – in this case ’shortness of breath‘ and ’heart palpitations,’ which are both symptoms of myocarditis that has been causally linked to mRNA COVID shots – the public should be warned, not kept in the dark. It raises questions about what else government health officials are hiding,” she added.

The free-text entries are not dated. Elizabeth Brehm, an attorney representing ICAN, said the group is seeking the dates of the reports from the CDC. The group does know that the entries are the earliest ones received by the CDC. V-safe was launched as the vaccines were rolled out in late 2020. The rest of the entries are expected to be produced on a rolling basis.

A CDC spokesperson declined to answer many questions, including through which date the entries were made.

“V-safe participants who reported that they received medical care after vaccination were called and encouraged to submit a VAERS report. If they submitted a VAERS report and the adverse events were classified as serious (as defined in the Code of Federal Regulations), CDC attempted to obtain additional information (medical records, hospital records, etc.) about the reported adverse event,“ the spokesperson told The Epoch Times. ”All data collected from VAERS is processed and analyzed for unusual patterns or unusually high numbers of rare and serious adverse events after vaccination.”

She said the information from VAERS helped detect problems the agency now acknowledges are caused by the vaccines, including myocarditis.


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