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Live blogging the FDA’s VRBPAC booster meeting
Welcome to the FDA Booster meeting 9/18 Update: Steve Brozak at Forbes has written a review of the meeting here. Dr. Sara Oliver is at it again. By using the tricks outlined by Dr. Mercola, she was able to lie and claim that unvaccinated people are 22-26 times as likely as fully vaccinated people to…
Pediatric Covid death numbers: can vaccinations of children be justified?
https://services.aap.org/en/pages/2019-novel-coronavirus-covid-19-infections/children-and-covid-19-state-level-data-report/ I’d like to start this discussion with data released by the AAP 2 days ago. To look at the granular data you must download the full reports, linked at the URL above as pdfs. Having dealt with US Covid data for over a year, the most germane message I have come away with is…
The Norwegian Medicines Agency believes that European countries will detect more rare cases of blood clots
Here is a google- translated article from Norway that tells it like it is about the A-Z vaccine, and why it is so hard for there to be transparency. Steinar Madsen, medical director at the Norwegian Medicines Agency, believes that several European countries will discover possible side effects of the AstraZeneca vaccine when they start looking…
White powder letters spook Washington as anthrax attack recalled/ Int’l Business Times
Curious timing of anthrax letters arriving at DC schools. Might they have been sent in support of the child vaccine trial? From IBT: Nearly 30 schools in Washington DC have received envelopes containing a mysterious white powder and with ‘AL AQEDA-FBI’ written on them, the Federal Bureau of Investigation said on Thursday. Preliminary testing has…
Quick explanation of FDA’s Emergency Use Authorization/Retraction for hydroxychloroquine and chloroquine
The Trump administration arranged on March 28 for 30-60 million tablets of hydroxychloroquine and certain (unapproved, unlicensed) chloroquine tablets to be donated by manufacturers to the National Strategic Stockpile (NSS) under an Emergency Use Authorization (EUA). The official who signed the EUA is the FDA’s Chief Scientist, Denise M. Hinton. Denise Hinton is a nurse with a master’s degree,…
NBSB urges pre-attack studies of anthrax vaccine in kids/ CIDRAP
From the NY Times, adapted by the Center for Infectious Disease Research and Policy, U Minnesota: Oct 28, 2011 (CIDRAP News) – An expert advisory panel today approved a recommendation that the US Department of Health and Human Services (HHS) develop a plan to study the use of anthrax vaccine in children before an attack…