The epoch times

FDA denies US Senator access to COVID-19 vaccine safety data.

U.S. officials ‌are refusing‌ to provide COVID-19 vaccine safety data to a U.S. senator.

Sen. Ron Johnson (R-Wis.) asked the U.S. Food and Drug Administration (FDA) for the results of analyses on ​data from the Vaccine Adverse Event Reporting System in January. The ⁤request came ‍after the U.S. Centers for Disease ⁣Control and Prevention (CDC) said none of the safety signals⁣ it identified for the COVID-19 vaccines were‍ “unexpected.”

The two agencies have run different types of analyses on the system’s reports, which are primarily made⁣ by health care professionals.

The CDC ran Proportional Reporting Ratio analyses, ⁢which involve comparing the number ‍of reported adverse events to the number of adverse events reported after vaccination with other vaccines.

The first ‌time the⁣ agency⁢ ran analyses using the method ‍for ⁣the COVID-19 vaccines, in 2022, hundreds of signals were triggered, files obtained by The Epoch ⁢Times⁣ show.

The FDA in 2021 started a ‌different type of analysis, called Empirical Bayesian (EB) data mining.

The Proportional Reporting Ratio ⁣results “were generally consistent with EB data mining, revealing no additional​ unexpected safety signals,” Dr. Rochelle ​Walensky, the CDC’s director⁢ at ​the time, told Mr. Johnson previously.

Mr. Johnson demanded answers on that claim, prompting the CDC to point him to the ‌FDA.

The FDA recently responded to Mr. Johnson, telling him that it cannot ​provide the information he seeks.

“FDA’s EB data mining analyses of adverse events contained in VAERS reports for COVID-19 vaccines ⁢are currently the subject of pending FOIA [Freedom of Information Act] litigation.​ FDA is unable to comment on pending litigation or provide information or⁣ data that is currently being considered in pending litigation,” the⁢ agency told the senator.

Mr. Johnson in ‍a ⁣ new letter told FDA Commissioner Dr. Robert Califf that the claim was wrong.

“As you are⁢ well aware, Congress has a right to information contained at U.S. federal agencies ‍as it conducts its constitutional oversight responsibilities,” Mr. Johnson said.

“It is outrageous that FDA would assert that pending litigation, and particularly FOIA litigation, would allow⁣ your agency to obstruct my congressional⁤ oversight,” he added. “Any pending litigation FDA may have⁢ relating to its EB data mining records has no ⁣bearing on its responsibility‌ to comply with a congressional request.”

Mr. Johnson said in the past ‍he’s repeatedly received from the government documents subject⁤ to litigation, ‍including from‌ the FDA’s parent agency, the U.S. Department of Health and Human Services (HHS).

He urged the⁣ FDA to produce the‍ EB data mining analyses by Sept. 20.

The FDA declined to immediately provide a ‍comment.

The agency was sued in⁤ January over its refusal to provide the results of the EB data mining ‌to The Epoch Times and⁢ the nonprofit Children’s Health Defense, citing exemptions in the Freedom of Information Act (FOIA).

Children’s Health Defense, the litigant, said that the refusal to ⁤provide ​the ​records was illegal.

In the last update ⁤in the case, the FDA said it has 150 ​responsive pages ⁣but that it ‍has to‍ do a “page-by-page, line-by-line review” to determine whether any information on the⁤ pages should be withheld, or redacted. The agency said it ‍is ​”facing an unprecedented FOIA workload” stemming from federal courts ordering it to release information it​ had said would be made public on the COVID-19 vaccines from Pfizer and Moderna.

Sen.‍ Ron Johnson (R-Wis.) speaks in Washington on May 15, 2023. (Madalina Vasiliu/The Epoch Times)

Ignored Questions

In⁢ another new letter, Mr. Johnson pressed the HHS ⁢on the program it administers to provide compensation to people injured by the COVID-19 shots.

Despite injections starting in December ⁤2020, ⁤and more than 1.5 million reports being lodged with the Vaccine Adverse Event Reporting System. HHS has compensated just four people, paying $8,592⁣ in total.

Others have been approved for compensation but the money ‌is still pending.

Mr. Johnson in⁣ April ⁤asked for more details on the program as the agency has not been ⁣forthcoming, including whether there are caps ​on the amount of money an injured person can receive and ⁤whether the government ⁣has advertised the program.

Mr. Johnson also demanded communications between HHS and COVID-19 vaccine⁤ manufacturers regarding⁤ compensation claims.

In a recent letter, HHS declined to answer many of the questions.

Mr. Johnson on Sept. ‌5 urged HHS Secretary Xavier Becerra ⁤to provide answers to all of his ⁢questions.

He pointed to how Mr. Becerra, when being vetted by the Senate, told senators that he would commit to providing a prompt response to⁣ any



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