The Jab has Serious Adverse Effects Including Myocarditis and Pericarditis

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‘Severely Flawed’: Cardiologist Criticizes FDA-Funded Study Suggesting Myocarditis, Pericarditis Risks from COVID-19 Vaccines

By Marina Zhang  June 18, 2022 Updated: June 19, 2022

Marina Zhang

Marina Zhang is based in New York and covers health and U.S. news. Contact her at marina.zhang@epochtimes.com.au.

 

Severely flawed” is a cardiologist’s verdict on a peer-reviewed study funded by the Food and Drug Administration (FDA) suggesting possible risks of developing myocarditis and pericarditis after getting a COVID-19 vaccine.

The recent FDA study published on June 11, 2022, used health insurance databases to identify myocarditis or pericarditis hospitalizations occurring in people aged 18 to 64 years, 1 to 7 days after a Pfizer or Moderna vaccine.

The authors found that though only 12 to 14 percent of the studied cohort were 18- to 25-year-olds, 33 to 42 percent of the myocarditis or pericarditis events occurred in people of this age group, suggesting that this age group may be linked with these vaccine adverse events.

“These results do not indicate a statistically significant risk difference between mRNA-1273 (the Moderna vaccine) and BNT162b2 (the Pfizer vaccine), but it should not be ruled out that a difference might exist,” the authors wrote in the study.

However, cardiologist Dr. Sanjay Verma told The Epoch Times that the study “using a 7-day limit for clinical endpoints” for myocarditis or pericarditis events after vaccination was “severely flawed.”

Verma, who practices in Coachella Valley, California, has been seeing many more heart problems since the vaccines rolled out.

“Continued increased risk [of myocarditis or pericarditis]” was found by the Centers for Disease and Prevention (CDC)’s Reports (MMWR) “even at 21 days after vaccination,” Verma wrote in an email.

Explaining that spike proteins have been found in blood circulation even four months after injection, “there is no medical justification for a 7- or 21-day cutoff,” he said.

Further, a British pre-print led by researchers from the University of Oxford found “continued increased risk of myocarditis after the booster,” which was not assessed by the FDA study.

Verma pointed out further issues in the study, stating that it does not include 12- to 17-year-olds, “who are the highest risk cohort.”

The same CDC MMWR report also found that the 12- to 17-year-old cohort has “2 to 3 times increased incidence compared to the 18- to 29-year-old cohort,” the doctor explained.

After the second dose, males aged 12 to 17 years had an incidence of 22.0 to 35.9 myocarditis or pericarditis cases out of 100,000 as compared to males aged 18 to 29 years who had an incidence of 6.5 to 15 cases out of 100,000, demonstrating that teens have a higher risk than adults.

Verma also added that “the study does not account for those who may have died before hospitalization,” who would not be “included in insurance claims database.”

Nonetheless, the cardiologist noted a “tremendous improvement” in the study for using health insurance databases as compared to prior FDA studies that exclusively relied on the Vaccine Adverse Event Reporting System (VAERS), which would most likely result in a lower incidence of cases.

“Overall, the findings of the study are interesting, but the above limitations likely yield significant underestimation of the true risk of myocarditis or pericarditis after COVID vaccination.”

“Public safety and ethical post market pharmacovigilance warrants more robust active longitudinal follow-up to ensure informed consent and appropriate risk stratification counseling,” Verma concluded.

Pfizer Saw So Many Adverse Events, They Had To Hire New Employees; Vaxxine Genocide Will Not Be Keep From The Masses Much Longer

Bombshell: Pfizer Saw So Many Adverse Events, They Had to Hire 2,400 NEW Employees to Process Them

Dr. Naomi Wolf: “[Pfizer] hid, they concealed, they redacted from disclosure, forced by court, the fact that they were processing so many adverse events in the first three months… that they had to hire 2,400 new employees. They hid that; they concealed it… the volume of bad outcomes, dangerous outcomes… there were so many [that] they couldn’t keep up with it with their own staff.”


ANOTHER COLLAPSE ON LIVE TV: THE VACCINE GENOCIDE WILL NOT BE KEPT FROM THE MASSES FOR MUCH LONGER

State-by-state breakdown of federal aid per COVID-19 case

HHS recently began distributing the first $30 billion of emergency funding designated for hospitals in the Coronavirus Aid, Relief, and Economic Security Act. Some of the states hit hardest by the COVID-19 pandemic will receive less funding than states touched relatively lightly, according to an analysis by Kaiser Health News.

The The first round of grants will be distributed based on historical share Medicare revenue, not based on COVID-19 burden. Therefore, hard-hit states like New York will receive far less per COVID-19 case than most other states.

HHS said it doled out the first slice of funding based on Medicare revenue to get support to hospitals as quickly as possible. The agency said the next round of grants “will focus on providers in areas particularly impacted by the COVID-19 outbreak,” rural hospitals and other healthcare providers that receive much of their revenues from Medicaid.

Below is a breakdown of how much funding per COVID-19 case each state will receive from the first $30 billion in aid. Kaiser Health News used a state breakdown provided to the House Ways and Means Committee by HHS along with COVID-19 cases tabulated by The New York Times for its analysis. link


 

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