(Undercover DC) Moderna Spikevax trial data show serious adverse events (SAEs) and death according to the first tranche of 13,685 pages of Moderna documents released Tuesday in response to a Freedom of Information Act (FOIA) filed by Defending the Republic (DTR). The documents are related to Moderna’s trials of the COVID-19 vaccine marketed as Spikevax. DTR filed a lawsuit in June 2022 against the U.S. Food and Drug Administration (“FDA”).
Just released –
14K pages of Moderna COVID-19 vaccine data related to adverse events.
Neurological disorders days after vaccination.
Details on post-vaccine deaths, heart attacks, pulmonary embolism – all not investigated by the “studies”https://t.co/UVjmxWBvOh
— Techno Fog (@Techno_Fog) July 20, 2023
According to DTR’s announcement, “DTR filed its FOIA lawsuit after the FDA denied the expedited production of Moderna COVID-19 records.” DTR states the FDA felt there was “no compelling need or urgency for the public to review this information.” In 2021, the FDA originally requested 55 years to “complete a FOIA request for data and information on the approval of Pfizer-BioNTech’s COVID-19 vaccine, Comirnaty.” The FDA later (Dec. 2021) “doubled down” and asked for 75 years to release Pfizer documents.
DTR’s agreement with the FDA stipulates the “production of approximately 24,000 pages of some of the most important records submitted by Moderna in support of its Biologics License Application (BLA). The FDA agreed to produce the remaining 10,000 pages “on a monthly basis, to be completed no later than December 31, 2023”, a total of 23,751 pages.
Internist and biological warfare epidemiologist, Dr. Meryl Nass, is on the advisory board for the Children’s Health Defense. She believes the information in the Moderna documents parallels the findings in the Pfizer clinical trial documents, also made available by DTR in a searchable format. Nass told The Defender the adverse side effects “likely were vaccine side effects.”
“Both the preclinical (animal) studies of Moderna and of Pfizer revealed skeletal abnormalities in the offspring of vaccinated mice and rats at higher-than-normal rates and revealed vaccine components traveled throughout the body into all organs.
Both the Pfizer and Moderna trial data in humans reveal concerning deaths and side effects that were attributed to other causes, but likely were vaccine side effects.”
Nass speculates that the rush to produce vaccines (Operation Warp Speed) may have contributed to what she believes was the FDA’s failure to “proper[ly] review” the clinical data.
Records Indicate Lack of Thoroughness in Moderna Trials
Defending the Republic states the Moderna “records also demonstrate the utter lack of thoroughness of these studies.” One of the criteria DTR listed as evidence of the lack of thoroughness was the inconsistent performance of an autopsy on those who died. The author of the DTR press release states:
“For example, a 56-year-old woman experienced “sudden death” 182 days after receiving the second Moderna dose. The cause of death was unknown, and no autopsy was conducted. It seems they purposely decided not to investigate suspicious deaths in case the Moderna vaccine might be the cause,”
According to the 218-page Moderna Clinical Study Report-16.2.7, of the listed treatment groups in the Death Listing, 1 participant was in the Placebo group, 3 were in the “Placebo-mRNA-1273” group, and 8 were in the “mRNA-1273” treatment group. In the two placebo groups, one autopsy was performed, one was not, and two were marked “UNK” or unknown.
In the mRNA-1273 treatment group, autopsies were performed on only 2 of the 8 who died. 3 of the 8 who died in the mRNA-1273 treatment group had no known risk factors for severe COVID-19, per the documents. Please refer to the gallery below for sourcedocuments:
“Both the preclinical (animal) studies of Moderna and of Pfizer revealed skeletal abnormalities in the offspring of vaccinated mice and rats at higher-than-normal rates and revealed vaccine components traveled throughout the body into all organs.
Both the Pfizer and Moderna trial data in humans reveal concerning deaths and side effects that were attributed to other causes, but likely were vaccine side effects.”
Nass speculates that the rush to produce vaccines (Operation Warp Speed) may have contributed to what she believes was the FDA’s failure to “proper[ly] review” the clinical data.
Records Indicate Lack of Thoroughness in Moderna Trials
Defending the Republic states the Moderna “records also demonstrate the utter lack of thoroughness of these studies.” One of the criteria DTR listed as evidence of the lack of thoroughness was the inconsistent performance of an autopsy on those who died. The author of the DTR press release states:
“For example, a 56-year-old woman experienced “sudden death” 182 days after receiving the second Moderna dose. The cause of death was unknown, and no autopsy was conducted. It seems they purposely decided not to investigate suspicious deaths in case the Moderna vaccine might be the cause,”
According to the 218-page Moderna Clinical Study Report-16.2.7, of the listed treatment groups in the Death Listing, 1 participant was in the Placebo group, 3 were in the “Placebo-mRNA-1273” group, and 8 were in the “mRNA-1273” treatment group. In the two placebo groups, one autopsy was performed, one was not, and two were marked “UNK” or unknown.
In the mRNA-1273 treatment group, autopsies were performed on only 2 of the 8 who died. 3 of the 8 who died in the mRNA-1273 treatment group had no known risk factors for severe COVID-19, per the documents. Please refer to the gallery below for source documents:
