Since 2022, Defending the Republic has been involved in Freedom of Information Act (FOIA) litigation against the Food and Drug Administration (FDA) relating to the production of data submitted by Moderna in support of its COVID-19 vaccine.
DTR is pleased to announce that the FDA has agreed to produce approximately 24,000 pages of the Moderna records by the end of the year. These documents include some of the most important information relating to the Moderna vaccine’s safety profile. Records relating to adverse events, totaling 13,685 pages, will be produced by July 17, 2023. After that, the FDA will be producing the remaining 10,000 pages on a monthly basis, to be completed by December 31, 2023.
DTR will release these documents to the public and to independent experts upon receipt. We expect these records to expose the deficiencies in the FDA’s approval process and to illuminate the many issues surrounding the Moderna vaccine. Stay tuned for more.
Relevant Filing: MOTION TO VACATE BRIEFING SCHEDULE (ECF NO.26)
Defending the Republic v. Food and Drug Administration: CIVIL ACTION NO. 3:22-1237-E