FDA Chief Admits He Knows People Killed by Covid 'Vaccines'

U.S. Food & Drug Administration (FDA) Commissioner Dr. Marty Makary has admitted that he knows people who were killed and injured by the same Covid mRNA “vaccines” that were approved for public use by his department.

However, Dr. Makary is now facing backlash after defending the continued rollout of mRNA-based injections, despite his admission and the mounting evidence of adverse reactions and ongoing public concerns about their safety.

In an interview with The Epoch Times, Makary urged Americans to “be patient” as the agency continues its investigation into the risks of these “vaccines,” including the newly approved Spikevax shot for children as young as six months old.

Makary’s comments come on the heels of widespread dissatisfaction over the FDA’s decision to approve a new mRNA vaccine for “high-risk” children, despite significant warning signs about the risks associated with these shots.

In his interview, Makary tried to reassure the public by stating that the FDA is no longer “blindly rubber-stamping” Covid “vaccines” each year.

He argued that rejecting the “vaccines” outright would undermine the government’s ability to force pharmaceutical companies to conduct proper randomized control trials and provide more conclusive data.

However, his insistence on waiting for future studies has raised alarms, especially considering the mounting body of evidence that already links the shots to serious health issues.

“People have a right to be angry,” Makary said, acknowledging the surging deaths and adverse events linked to the mRNA injections.

“I personally know of people who have been injured by the vaccine,” he shared.

“I personally know of friends who have lost a loved one from the mRNA Covid vaccine.

“They have been deceived.”

Makary’s statement echoes a sentiment that is widely shared among vaccine critics, who argue that the continued approval of these shots despite growing safety concerns is deeply problematic.

The FDA’s current adverse event databases, Makary claimed, are “too clunky” to provide meaningful insights.

However, this has done little to quell public distrust in the agency’s handling of the situation.

“Be patient with us as we do this the proper scientific way,” Makary urged, suggesting that in “the next six months, these trials can be done.”

But this promise to conduct further studies has left many wondering why the FDA continues to approve new mRNA shots for children and other high-risk populations while already acknowledging the potential dangers.

WATCH:

By the end of June, the federal Vaccine Adverse Event Reporting System (VAERS) had reported nearly 39,000 deaths and over 220,000 hospitalizations related to the Covid “vaccines.”

VAERS has also logged significant numbers of heart attacks and myocarditis cases caused by the shots.

However, studies have warned that VAERS data is massively underreported and only represents around 1% of the true number.

Researchers from the CDC have acknowledged the “high verification rate” of these reports, further fueling skepticism about the safety of mRNA “vaccines.”

The latest studies have linked the shots to serious conditions like myocarditis, Guillain-Barré syndrome, and even cancer-related deaths.

Japanese researchers also recently sounded the alarm after finding “statistically significant increases” in cancer mortality following the third dose of the mRNA jab.

Despite this mounting evidence, the FDA approved a new round of mRNA-based Covid shots in July, offering them to individuals over 65 or those aged 12-64 with underlying health conditions.

The approval has sparked criticism from vaccine critics, who argue that it is an overreach by the government to force these “vaccines” on vulnerable populations, especially when so many questions remain unanswered.

Dr. Makary and other health officials, including Dr. Vinay Prasad, have backed away from blanket recommendations for all Americans to receive the Covid shots.

However, the ongoing approval of new shots for high-risk individuals, along with the FDA’s decision to approve a vaccine for children, has left many questioning whether the government is truly acting in the best interests of public health.

As the debate continues, many are calling for a reevaluation of the mRNA “vaccine program,” citing the significant risks associated with these shots and the lack of transparency from the FDA and other health agencies.

“Be patient,” may be what Makary says, but for many Americans, their patience is running thin.

The people are demanding accountability for the decisions that have already caused so much harm.