Posted on 10/28/2021 1:30:17 PM PDT by TedMartin
Let’s see...
+99.9% child survival rate.
“HEY! We’re missing a profit center here!”
“But what about side effects like heart issues, blood clots, etc.?”
“HEY! Great idea, we can sell them Kid Blood Clot medication and Heart Attack Preventors!!”
The old joke in the contracting business is “Fast, good, and cheap — pick the two that you want.”
Just evil, isn’t it?
350 state school districts intend to hold vaccination events to get kids vaccinated
Some parents look forward to getting children vaccinated as eligibility may be days away
12th birthday celebration for CNY middle schooler involved COVID-19 vaccine dose
Hey, they’re only kids! They can’t vote yet!! (and many likely will never get to the age they could)
That is so true.
Can I steal that?
Free to use.
It appears this is a new ingredient in the Pfizer shot, but has been in the Moderna one.
Thx
From a poster on Instapundit open thread a few minutes ago:
thecoldeye • 2 minutes ago
Kid Pfizer Vaccine Trivia
From FDA Briefing Document page 20 under “Safety”
Due to reactogenicity observed in the initial 4/16 participants assigned to the 30 µg dose
level group after they received both doses of BNT162b2 (Section 3.4.1), an Internal Review Committee decision was made for the remaining 12/16 participants assigned to the 30 µg dose level group to receive
the second dose based upon selection of the dose-level for Phase 2/3 ie, 10 µg. These
subjects will not be discussed further. END QUOTE
If you need a translation, Pfizer spells out what this means in Section 3.4.1: “Systemic events at the
30-µg dose level were deemed unacceptable, leading to the discontinuation of this dose level.” END QUOTE
Coldeye editorial comment: I translate “were deemed unacceptable” to mean “it was so obvious this dose was hurting children, that we changed the protocol mid trial.” I have no problem with any of this. How do we find out what dose to give? One way is to find out how much hurts people and back down from there. Sorry, it’s hard to avoid this kind of bracketing when you’re in a hurry.
Here’s what I object to. The kid trial makes VERY clear that 30 micro is too much. However, in adults, Pfizer gives 30 micro to adults who weigh 300 pounds and adults who weigh 85 pounds. In light of the kid trial, don’t you think Pfizer should be asked to re examine the 30 micro dose in 85 pound adults?
Evil.
From another poster on Instapundit open thread about an hour ago:
thecoldeye • an hour ago • edited
More Kid Pfizer Vaccine Trivia
Here is why Pfizer wants an Emergency Use Authorization for kids 5 to 12
(from FDA briefing document page 7):
Based on Centers for Disease Control and Prevention (CDC) data, among children 5 to
<12 years of age there have been approximately 1.8 million confirmed and reported
COVID-19 cases and 143 COVID-19-related deaths in the US through 14 October 2021. In
this same age group, there have been 8622 COVID-19 related hospitalizations through
18 September 2021. END QUOTE
Coldeye commentary: Pfizer has not described an emergency.
Here are the facts: About 83% of pediatric ICU patients had “significant” pre existing comorbidities. (JAMA Ped Shekerdemian)
For all pediatric hospital admissions, the average length of stay is only 2 or 3 days. (CDC, Delahoy)
Virtually all of the deaths involve kids with very serious co morbidities.
THIS IS NOT AN EMERGENCY.
Using the CDC’s own excess deaths data, you can look at deaths under 25 for the past five years AND YOU CANNOT IDENTIFY YEARS 2020 and 2021. For under age 25, 2020 and 2021 are INDISTINGUISHABLE from years before covid. If you want to see what an EMERGENCY looks like, look at CDC excess deaths data for age 85 and older.
Blood lines
“Pass thy seed through...”
Nephilim
CRISPR
As in the Days of Noah
Only 8 pure DNA souls left.
Can you add me to your ping list?
“Doctor on FDA panel says only way to learn about COVID vaccine effects in children is to ‘start giving it’”
The FDA has fallen a long way since Dr Francis Kelsey refused to approve thalidomide because there were no studies on pregnant animals submitted with the application. It was her first week working at the FDA and her first project.
👍🏻👍🏻
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