Food and Drug Administration

FDA Restricts J&J COVID Vax Due to ‘Life-Threatening’ Side Effects

The vaccine was found to cause potentially fatal blood clots.

HHS Chief: Taxpayers Should Fund Surgically Removing Kids’ Genitals

The Joe Biden administration in Washington is so committed to the transgender ideology, including the surgical procedures that mutilate the body parts of children and leave them permanently sterile, that his spokeswoman has threatened those who oppose it.

25% Increase in ‘Cardiovascular Events’ in Young People After Vax Rollout: M.I.T. Study

Peer-reviewed study findings "raise concerns regarding vaccine-induced undetected severe cardiovascular side-effects and underscore the already established causal relationship between vaccines and myocarditis, a frequent cause of unexpected cardiac arrest in young individuals."

40 Times More ‘Serious Side Effects’ Than Official Government Records Indicate: Germany

Russian news outlets call out United States pharmaceuticals as Pfizer released massive amounts of data about their vaccine.

COVID Vax Animal Trials Reveal Potential Impact on Major Organs

Judicial Watch today announced it received 466 pages of records from the U.S. Department of Health and Human Services (HHS) regarding biodistribution studies and related data for the COVID-19 vaccines that show a key component of the vaccines developed by Pfizer/BioNTech, lipid nanoparticles (LNPs), were found outside the injection site, mainly the liver, adrenal glands, spleen and ovaries of test animals, eight to 48 hours after injection.

Patients Taking Pfizer’s Anti-Viral Seeing Recurrence of COVID Symptoms

FDA reevaluating the reports of "viral load rebound" following concerns about the antiviral drug.

Pfizer Tests Lyme Disease Vaccine on Kids, but Experts Question Need

Pfizer on Tuesday said results of Phase 2 clinical trials of its experimental Lyme disease vaccine delivered “positive” results, including among pediatric trial participants.

Moderna Seeks 1st COVID Shot for Children Under 6

Moderna on Thursday asked U.S. regulators to authorize low doses of its COVID-19 vaccine for children younger than 6, a move toward potentially allowing shots for millions of youths by summer.

FDA Rubber-Stamps Remdesivir for Infants Without Evidence of Safety, Efficacy

The U.S. Food and Drug Administration (FDA) on Monday approved the use of the antiviral therapy, remdesivir, to treat COVID-19 in infants four weeks and older.

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