Johnson & Johnson

Crenshaw financed by Boeing, Lockheed Martin, Raytheon, and more.

New hepatitis vaccine hit market in March—now CDC wants to remove "obstacle" of risk assessment before injecting patients with hepatitis vaccine.

The Food and Drug Administration (FDA) has limited the authorized use of the Johnson & Johnson vaccine due to rare blood clots.

The vaccine was found to cause potentially fatal blood clots.

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.

VAERS data show total of 1,247,131 reports of adverse events from all age groups following COVID-19 vaccination.

After going a full administration without a new war to fill their coffers, the D.C. defense industry has finally found their next big prize.

"Antibodies produced by vaccinated and boosted people may not stop omicron SARS-CoV-2 strain from entering cells as well as it stops original virus," say Johns Hopkins researchers.

The Centers for Disease Control and Prevention (CDC) today released new data showing a total of 1,237,647 reports of adverse events following COVID vaccines were submitted between Dec. 14, 2020, and April 15, 2022, to the Vaccine Adverse Event Reporting System (VAERS). VAERS is the primary government-funded system for reporting adverse vaccine reactions in the U.S.

"Our clients' portfolios—which reflect the global economy—cannot reach net zero without sustained and consistent government policy, accelerated technological breakthroughs, and substantial adaptation in corporate business models," says BlackRock.