A physician is suing the FDA for its lack of action to inform consumers taking selective serotonin reuptake inhibitors (SSRIs) and serotonin-norepinephrine reuptake inhibitors (SNRIs) about potential long-term side-effects. These drugs are widely-used antidepressants. A citizen petition requests that the FDA […]
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The Select Subcommittee on the Coronavirus Pandemic is conducting oversight of Covid-19 vaccine development, and investigating alleged potential political influence the Biden Administration wielded over the Covid-19 vaccine approval process. Republicans on the committee have said they are concerned the
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“If the data were strong enough to ban Red 3 in cosmetics and external drugs 30 years ago, they’re surely strong enough to ban it today in foods, oral drugs, and dietary supplements.” Dr. Peter Lurie, CSPI President The following
Scientists urge FDA to ban cancer-causing dye used in hundreds of candies and foods Read More »
The following is an excerpt from The Vaccine Reaction. The U.S. Food and Drug Administration (FDA) has refused a Freedom of Information Act (FOIA) request to release the autopsy results of people whose deaths were reported to the Vaccine Adverse
FDA withholds autopsy results of those who died after Covid-19 vaccination Read More »
Sen. Marsha Blackburn (R-Tenn.) is asking the FDA to provide information about the controversial use of certain puberty blockers in children who suffer from gender dysphoria and wish to resemble the opposite sex. Blackburn says she was motivated to write
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The following is an excerpt from The Vaccine Reaction. The U.S. Food and Drug Administration (FDA) issued a safety communication on Sept. 8, 2022 warning that certain cancers may develop in scar tissue “capsules” that form around breast implants. Cancers
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The following information is from the FDA re: its decision to limit use of J&J Covid-19 vaccine due to blood clot risk. Today, the U.S. Food and Drug Administration has limited the authorized use of the Janssen COVID-19 Vaccine to
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FDA Adviser Dr. Caleb Alexander of John’s Hopkins talks about Aducanumab/Aduhelm: a groundbreaking Alzheimer’s treatment sent to market in one of the most controversial FDA approvals ever.
