38 out of 171 Moderna Booster recipients developed COVID19

Moderna is asking the United States FDA to allow millions of people to receive boosters. The discussion from the FDA is here:

https://www.fda.gov/media/152991/download

It is quite ridiculous that Moderna has the chutzpah to ask to vaccinate millions, based on studying two subgroups of about 170 people in each. But this is Covidland, so no surprise here.

Now look at page 42:

As described in Section 4.2.5, 38 cases of COVID-19 infection occurred after booster vaccination among the 171 booster dose participants in the 100 µg-primed group of study P201 through the data cutoff date for the EUA amendment submission. Due to limitations in study design (no control group, exploratory COVID-19 endpoint, lack of case definitions, lack of systematic collection of COVID-19 symptoms, and differences in transmission rates in Part A vs Part B of study P201), no inferences can be made based on these data from P201 Part B.

So 38 out of 171 fully vaxxed, and boostered participants, got Covid19. And instead of running away ashamed, Moderna is asking to give us a booster so ineffective?

Is it merely ineffective, or does the booster actually enhance infectivity?

This rate of 22% Covid cases in this tiny Moderna trial, for just a few months after fully vaxxing and boostering, is almost TWICE greater than the total rate of Covid cases in all Americans, FOR ALL TIME. (45 million out of 220 million).

And that 22% occurred in the short period after getting fully vaxxed, and then having been boostered, and looked at in the study. If this is not a failure, I do not know what is a failure in COVIDland.

There is more shocking stuff in the unsolicited adverse effects section, that I will discuss later.

The adverse effect was ONE pregnancy that ended in a spontaneous abortion.

The subject experienced a spontaneous abortion 52 days after vaccination at an estimated 8 weeks gestation (10 months and 11 days after the first prime dose of 100 µg mRNA-1273 and 9 months and 12 days after the second prime dose of 100 µg mRNA-1273). This event was not considered by the investigator or Moderna to be related to study vaccination.

That was the ONLY pregnancy in the entire trial. Is that a joke or what?

How can the FDA approve this in good conscience?