Obviously Covid and the Covid Regime haven’t gone away. Damage/Information control is still very much in evidence. As a result we have to read between the lines. But these lines don’t seem to me very difficult to read between—pasted in from FR:
EU Investigating mRNA Vax Side Effects
https://thepalmierireport.com ^ | February 11, 2022 | By Jacob PalmieriThe European Union is now looking into if mRNA vaccines are causing vaccine side effects in women.
The two mRNA vaccines are Moderna and Pfizer.
EU investigates reports of menstrual disorders after mRNA COVID shots https://t.co/X9bwgijZji pic.twitter.com/s3AzVZbm5O
— Reuters (@Reuters) February 11, 2022
From Reuters:
The European Medicines Agency’s safety committee said on Friday it was reviewing reports of heavy menstrual bleeding and absence of menstruation from women who had received COVID vaccines from Pfizer (PFE.N)/BioNTech (22UAy.DE)and Moderna (MRNA.O).
The assessment was in view of reports of menstrual disorders after receiving either of the two vaccines, both based on messenger RNA technology, and it was not yet clear whether there was a causal link, the agency said.
It was not yet clear whether there was a causal link between the vaccines and the reports, the agency said.
And:
Pfizer and FDA pull back from plan to expedite review of Covid-19 vaccine in young children
STAT ^ | February 11, 2022 | MATTHEW HERPER, NICHOLAS FLORKO AND HELEN BRANSWELLPlans to attempt to authorize the Pfizer/BioNTech Covid vaccine for children under 5 before full data are available appear to have run aground.
The Food and Drug Administration on Friday canceled a key meeting planned for next week to discuss the submission, saying that the delay “will give the agency time to consider … additional data.”
Pfizer and BioNTech had previously said they would submit an application for the use of a two-dose vaccine at the FDA’s request, despite concerns that that regimen was not shown to be effective in clinical trials. Now Pfizer and BioNTech say that they will extend their submission until data on a three-dose regimen are available — expected in early April.
“Based on the agency’s preliminary assessment, and to allow more time to evaluate additional data, we believe additional information regarding the ongoing evaluation of a third dose should be considered as part of our decision-making for potential authorization,” the agency said in a statement.
The FDA had been publicly contemplating an aggressive timeline for making the shots available to younger children, even before full data are in on an expected three-shot series they would likely eventually receive.
Pfizer announced late last year that in a clinical trial of children aged 2 to 4 years old, two doses of vaccine failed to generate antibody levels on par with those seen in people aged 16 to 25 after two shots. Paradoxically, two doses given to infants aged 6 months to 23 months did generate antibody levels similar to those seen in the 16- to 25-year-olds, levels that are deemed to equate with protection.
(Excerpt) Read more at stocks.apple.com ...
The magnitude of the evil inherent in jabbing 6 mos to 4 year old children with this poison is almost incomprehensible. So many deceived and so many lives lost or permanently damaged - all for nothing more than money, the love of which we can now see is truly the root of the evil.
Pfizer trying to get ahead of the .....https://www.newstarget.com/2022-02-11-pfizer-warns-investors-tidal-wave-potential-fraud-revelations.html