FDA Refuses To Add Death To Label As Side Effect
Do you believe RFK Jr. is doing a good job as new HHS Director or is he missing the big picture?
I don’t understand? If I was given such a huge responsibility, I’d be taking the large steps first. I would out right ban the vaccines. These little steps to change the conversation won’t work. You need to be a lion. Not a mouse.
These vaccines are clearly killing people and have been for years. Yet, “Sssshh! don’t tell anyone!” philosophy out of DC is the game from the new director. Come on man! These are people’s lives. This has been documented for years. What are you afraid of?
Is Bobby being silenced? Strong armed? For God’s sake you are the top dog, not a Weiner!
Impatient media anchors including Steve Gruber, are making more firm assertions that new administration is not managing regulatory affairs on COVID-19 properly. It looks like the same Biden administration corruption with violation of regulatory law for COVID-19 vaccines.
A drug or vaccine should have a black box (boxed) warning for a fatal side effect. The FDA uses black box warnings to highlight serious and potentially life-threatening risks associated with prescription drugs, and they are the strictest labeling requirements the agency can mandate. These warnings are crucial for informing healthcare providers and patients about potential dangers, leading to more informed prescribing decisions and safer patient outcomes.
As of 2022, over 400 medications currently carry boxed warnings. Here is one put on the package insert for Uloric, a popular medicine to prevent gout. With 19,403 American COVID-19 VAERS deaths (as of April 25, 2025) and fatal, autopsy-proven vaccine-induced deaths in the peer-reviewed literature, why won’t the FDA under the current administration fairly inform patients of fatal side effects? McCullough and Gruber discuss this and more on Real America’s Voice, The Steve Gruber Show.