Following the Food and Drug Administration’s (FDA) licensing of Moderna’s COVID-19 vaccine, they were requested by law firm Siri & Glimstad on behalf of their client Public Health and Medical Professionals for Transparency (PHMPT), to release under the Freedom of Information Act (FOIA) all documents they used to justify this products full approval. The courts force the FDA to release the public documents at a rate of 180,000/month – READ
At the same time as the Moderna documents were released, so too were the Pfizer 12-15 aged group documents.
The DailyClout/WarRoom possie of volunteers have began analysing the documents just has they have been doing, and continue to do for the Pfizer BioNTech FOIA’d documents. Below I will attempt to capture the reports and other revelations relating to these documents.
Other additional Freedom of Information requests for Moderna documents will also be included below such as Defending the Republic (DTR) and the Informed Consent Action Network (ICAN).
Moderna FOIA document revelations in reverse chronological order
Links continuously being added
2024
March 10, 2024 – ICAN: New Case Reports Released for Pfizer Ages 12-15 and Moderna Ages 18+ which Show Myocarditis, Appendicitis, Intestinal Perforation, and More in the child trial participants – READ
- The release included 112,345 pages of Moderna Spikevax documents, which include several case reports noting gastrointestinal adverse events. Notably, intestinal perforation has been linked to thrombosis and COVID-19 infection and, yet, in each of the following cases, the adverse event was deemed “unrelated” to the clinical trial. [Because Pfizer said so!]
February 26, 2024 – ICAN: December Release of FDA’s Moderna and Pfizer Data Sheds Further Light on the Purported “Safety and Efficacy” of COVID-19 Vaccines – READ
- Out of 200K pages released in December 2023, 1,069 pages related to Moderna’s Spikevax
- They showed “solicited serious Grade 3 or Grade 4 systemic adverse reactions were 4.5 times greater in the vaccine arm (17.4%) versus the placebo arm (3.8%)”
- Moderna made clear that it had no intention of providing the additional short or long term safety data that was requested by the FDA in Sept 2021! “Moderna claimed that analyzing the additional data would “not serve any additional analytical purpose” and additionally admitted “[t]here was no systematic collection or analysis of [adverse reactions]” in the additional data.”
- Natural immunity in placebo arm due to history of SARS-CoV-2 infection at the start of the study resulted according to Moderna in “too small” COVID-19 cases numbers so “the results can not [sic] be interpreted in a meaningful way.” Natural immunity was dismissed
- The FDA was very interested in the incidence of herpes zoster (shingles) after vaccination, maybe due to a previous fatal case?
February 19, 2024 – Report 95 & 96: mRNA COVID-19 Shots – ‘Vaccines’ or Gene Therapy Products? – PART 1, PDF, & PART 2, PDF
- How a REGULATOR like the FDA defines a drug drug product to be considered a “vaccine” or a “gene therapy” determines which regulatory pathway and as such which advisory committee reviews the product and what steps the drug approval process involves. [THIS IS KEY as the vaccine was assessed as a PLATFORM technology, not a single product]
- The FDA has a specific committee for gene therapies — the Cellular, Tissue, and Gene Therapies Advisory Committee (CTGTAC), that wasn’t used for Moderna’s “gene therapy” product that was called a “vaccine”
- Moderna in their June 30, 2020Q2 Report they state (pg 70) that “mRNA is considered a gene therapy product by the FDA…” yet the FDA and CDC told the public it was an mRNA COVID-19 “vaccine,”. In addition Moderna stated “no product in which mRNA is the primary active ingredient has been approved, the regulatory pathway for approval is uncertain. The number and design of the clinical trials and preclinical studies required for the approval of these types of medicines have not been established,…” They also state “We have incurred significant losses since our inception and anticipate that we will continue to incur significant losses for the foreseeable future….As of June 30, 2020, we had an accumulated deficit of $1.74 billion.” [3] – TIMELINE
- How convenient the global regulators allowed mRNA gene therapy products to enter a regulatory pathway as a “vaccine” product under EMERGENCY USE legislations.
2023
November 14, 2023 – Daily Clout: Report 91: FDA Based Moderna’s mRNA COVID Vaccine Approval on Test of a Completely Different Non-COVID Vaccine. Only Males Included in Test. – READ
- Moderna’s biodistribution study was for a completely different vaccine. ““A biodistribution study was not performed with mRNA-1273 vaccine [SPIKEVAX]. Results from the biodistribution study of a different vaccine [(mRNA-1647)] . . . were submitted in support of SPIKEVAX” – even though “there are important differences between the two mRNA drugs.”
- In spite of this substitution, on December 18, 2020, the FDA authorized emergency use of Moderna’s COVID-19 mRNA drug (FDA 2020), and on January 31, 2022, the FDA fully approved Moderna to manufacture and distribute SPIKEVAX (FDA 2022b).
August 11, 2023 – Daily Clout: Report 80: Moderna mRNA COVID-19 Injection Damaged Mammals’ Reproduction: 22% Fewer Pregnancies; Skeletal Malformations, Pain, Nursing Problems in Pups. FDA Knew, Yet Granted EUA– Wahl of Team 5 – READ
August 1, 2023 – First batch of PHMPT Moderna FOIA documents released – HERE
July 23, 2023 – Epoch Times: ‘Serious Doubt’ About COVID-19 Vaccine Safety After Forced Release of 15,000 Pages of Clinical Trial Data: Legal NGO – Defending the Republic (DTR) – READ
July 19, 2022 – Defending the Republic via Daily Clout: More Horrors, This Time From Moderna – Defending the Republic Lawsuit Obtains Almost 15,000 Pages of Moderna COVID-19 Vaccine Clinical Trial Documents – READ, TWEET
May 13, 2023 – Aaron Siri Substack | Injecting Freedom: FDA Ordered To Produce Moderna C-19 Vaccine And Pfizer Adolescent C-19 Vaccine Data At Average Rate Of 180,000 Pages Per Month – READ
April 8, 2023 – PRESS RELEASE: DEFENDING THE REPUBLIC vs FOOD and DRUG ADMINISTRATION – READ
2022
July 18, 2022 – Trial Site News: Moderna FOIA Bombshell Reveals Alarming Problems with FDA Approval of SPIKEVAX – with Alexandra (Sasha) Latypova – WATCH
2020
September 4, 2020 – ICAN FOIA: NIH Officials Stand to Earn Millions from Moderna Vaccine – READ
