Forced Release of Clinical Trial Data Raises ‘Serious Doubt’ about Covid Vaccine Safety

The U.S. Food and Drug Administration (FDA) has been forced to release thousands of pages of data related to the clinical trials of mRNA Covid vaccines.

Conservative public interest advocacy group Defending the Republic (DTR) has obtained almost 15,000 pages of Moderna’s COVID-19 vaccine clinical trial data.

The organization is now warning that the data shows an “utter lack of thoroughness” of the trials and calls the vaccine’s safety into “serious doubt.”

The group obtained the documents as a result of successful Freedom of Information Act (FOIA) litigation against the FDA.

DTR announced that it will now be releasing nearly 15,000 pages of documents relating to testing and adverse events associated with “Spikevax,” Moderna’s mRNA COVID-19 vaccine.

Since 2022, the group has been involved in litigation against the FDA relating to the production of data submitted by Moderna.

The pharmaceutical giant submitted the trial data in support of its application to federal regulators for approval of its vaccine.

As a result, the FDA agreed to produce around 24,000 pages of the Moderna records by the end of this year.

The 15,000 pages obtained so far are the first installment.

The records, some of which relate to adverse events related to the vaccine, include essential information related to the safety profile of Spikevax.

The injection was first authorized for emergency use in the United States in December 2020 and in January 2022 received full approval for adults.

“The public can be assured that Spikevax meets the FDA’s high standards for safety, effectiveness, and manufacturing quality required of any vaccine approved for use in the United States,” Acting FDA Commissioner Dr. Janet Woodcock said in a statement earlier this year.

But the newly revealed data calls this view into question.

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The advocacy group says that the tens of thousands of pages of clinical trial data released by the FDA supports the conclusion that there is “serious doubt” about both the safety of Spikevax and the FDA’s standards for approval.

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By Nick R. Hamilton

Nick has a broad background in journalism, business, and technology. He covers news on cryptocurrency, traditional assets, and economic markets.

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