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FDA Blocked Studies on Vaccine Safety and Efficacy

The Food and Drug Administration blocked studies demonstrating the safety of several vaccines, according to a New York Times report. Two of the withdrawn studies found that serious side effects from commonly used COVID vaccines were rare. A Department of Health and Human Services spokesman said the studies were withdrawn because the authors drew broad conclusions not supported by the underlying…

JE
manilatimes.net
2 sources·May 8, 5:50 AM(1 day ago)·2m read
FDA Blocked Studies on Vaccine Safety and Efficacynbcnews.com
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The Food and Drug Administration blocked studies demonstrating the safety of several vaccines in recent months, the New York Times reported. The studies were carried out by the Department of Health and Human Services in recent years. Two of them found that serious side effects to commonly used COVID vaccines were rare.

Scientists in the department analyzed millions of patient records for the research, which cost taxpayers millions of dollars. In October the scientists were ordered to withdraw the two studies even though medical journals had already accepted them. A Department of Health and Human Services spokesman said in an email that the studies were withdrawn because the authors drew broad conclusions that were not supported by the underlying data.

The spokesman added that the FDA acted to protect the integrity of its scientific process and ensure that any work associated with the agency meets its high standards.

During the 2024 presidential election campaign President Donald Trump promised to give an anti-vaccine activist a prominent role in the White House’s health care section. Days after winning the election Trump announced he would nominate that activist for Secretary of Health and Human Services.

The Senate confirmed the appointment in a vote that largely followed party lines. Since taking office the secretary has made changes to how the U.S. government handles vaccines. In February 2025 the secretary directed the Centers for Disease Control and Prevention to stop advertising flu vaccinations.

In December an advisory committee made up largely of the secretary’s appointees voted to end the CDC’s recommendation that newborns receive Hepatitis B vaccinations. The secretary also removed all 17 members of the Advisory Committee on Immunization Practices which advises the CDC on vaccines.

One public health official described the action as a departure from normal process.

Party have expressed skepticism about vaccinations especially those related to COVID. Claims that vaccines cause autism are not supported by scientific evidence but gained attention during the pandemic along with other health-related misinformation.

The FDA’s decision to block the studies comes amid these broader discussions about vaccine policy. The New York Times reported the development citing the Department of Health and Human Services spokesman who confirmed the withdrawal of the research.

Key Facts

FDA blocked studies
on safety of several vaccines
Two studies withdrawn
found rare serious side effects from COVID vaccines
Studies analyzed
millions of patient records at cost of millions of dollars
Spokesman cited
broad conclusions not supported by data
Senate confirmed
appointment in party-line vote

Story Timeline

4 events
  1. May 8, 2026

    New York Times reported that FDA blocked vaccine safety studies.

    1 source@Jerusalem_Post
  2. December 2025

    Advisory committee voted to end CDC recommendation for newborn Hepatitis B vaccinations.

    1 source@Jerusalem_Post
  3. February 2025

    Secretary directed CDC to stop advertising flu vaccinations.

    1 source@Jerusalem_Post
  4. October 2025

    Scientists ordered to withdraw two studies on COVID vaccine side effects.

    1 source@Jerusalem_Post

Potential Impact

  1. 01

    Withdrawal may reduce publicly available research on COVID vaccine side effects.

  2. 02

    Replacement of advisory committee members may shift future federal vaccine guidance.

  3. 03

    Changes to CDC vaccine recommendations could alter vaccination rates for flu and Hepatitis B.

  4. 04

    FDA action aims to maintain standards for agency-associated scientific work.

Transparency Panel

Sources cross-referenced2
Confidence score65%
Synthesized bySubstrate AI
Word count381 words
PublishedMay 8, 2026, 5:50 AM
Bias signals removed2 across 2 outlets
Signal Breakdown
Framing 1Editorializing 1

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