Why would that study require a control group? They would just be tracking the variability in mens sperm counts, which I'm sure is data that's already available.
Because the sample size was too small. And because control groups help benchmark and contextualize results.
But mainly because mandating a shot requires intense scientific vigor to ensure that the product is safe. An uncontrolled trial with n=45 is not that.
The researchers even stated as much:
The limitations of the study include the small number of men enrolled; limited generalizability beyond young, healthy men; short follow-up; and lack of a control group. In addition, while semen analysis is the foundation of male fertility evaluation, it is an imperfect predictor of fertility potential.
You tried to use that study to prove that the government conducted fertility studies prior to the vax mandate. That study wouldn't qualify.
Both of these studies I quoted were just the first results I grabbed for the time frame before the mandate. There are several others for both. Here's a different fertility one.
Abstract. Some reproductive-aged individuals remain unvaccinated against coronavirus disease 2019 (COVID-19) because of concerns about potential adverse effects
academic.oup.com
Over 2,100 participants. This studied the impact of fertility after receiving the covid vaccine and also contracting covid in both males and females. The only association was a temporary drop in fertility amongst men who caught covid.
This study is irrelevant to the topic at hand.
Vax mandate declaration: SEP 2021
Study published: JAN 2022
Ivermectin was never banned. If you wanted it and your doctor thought it might be effective or didn't care that it wouldn't be, you were free to use it.
Objectively false. Here are some stories from FL, TX, IL, TX, VA, and AK.
A judge recused herself in a hearing for an emergency petition to let a dying man take ivermectin, which has not been proven to be an effective COVID treatment.
www.jacksonville.com
The family of a Richmond, Texas veteran, who died of COVID-19, say a Sugar Land hospital refused to give the 74-year-old a court-ordered treatment of Ivermectin.
www.fox26houston.com
ELGIN, Ill. — The family of a suburban man who is seriously ill with COVID-19 has filed an emergency appeal trying to force doctors to treat him with the controversial drug ivermectin.Sebastrian Ab…
wgntv.com
A COVID-stricken rabbi won't be treated with ivermectin after his wife drops lawsuit against an NYC hospital.
www.bizpacreview.com
Funeral on Friday for Anchorage man, William Topel, who was denied Ivermectin treatment at Providence Alaska Medical Center.
alaskawatchman.com
1) Here's a different one that was completed in February of 2021. 35,000+ pregnant women studied. Split between Pfizer and Moderna. 14% of the total being vaccinated before even becoming pregnant.
This is not a study. It is an observation using unrelated systems, V-Safe and VAERS. It compared the number of V-Safe enrollees vs. VAERS reports - there's no correlation between the two.
First - do you believe that VAERS is a reliable source of vaccine safety information, yes or no?
Second - the study did not mention the VAERS URF (under-reporting factor), which is estimated between 31x - 99x based on two studies I could find (I trust the 31x much more since it used Pfizer trial data and provided the methodology for calculating URF). Maybe you can find some better data on URF, but to simply ignore it is bad science.
- https://digital.ahrq.gov/sites/defa...ion/r18hs017045-lazarus-final-report-2011.pdf
- https://cf5e727d-d02d-4d71-89ff-9fe...d/adf864_0490c898f7514df4b6fbc5935da07322.pdf
The only way the medical community would ever use this study is if they wanted to shortcut the traditional methods for ensuring safety. And so here we are, back at shortcuts.
2) No. Do you think drug companies just develop drugs and then wait for the FDA to test them before they figure out if they're safe? Pfizer developed their vaccine then tested it to make sure it was safe. They made their data and methodology publicly available just like with any other drug they take to market.
Firstly, no, that's not how drug safety testing works.
Secondly, no, they didn't make their data and methods publicly available. The FDA and Pfizer tried to hide the trial results until they were forced to disclose them.
3) Yes. The FDA approved the vaccines. It's not up to Pfizer to give Biden the go ahead.
Your bias clouds objectivity. No, mid-trial data cannot inform policy. It's ridiculous to claim otherwise.
4) I'm not a statistician. I don't have the knowledge to critique that aspect either way.
The objectively answer, again, is no. n=350 is not sufficient data to base a mandate upon.
5) I believe that's actually because of the study I linked in point 1). That study didn't have enough pregnancies carried to completion yet because 13.5% were pre pregnancy, 30% first trimester, and 43% in second trimester meant only ≈800 had actually given birth so far. So they supplemented it with this Pfizer study that was mostly late term pregnancies so they could study the babies sooner too.
No, that study neither proves or disproves causal link because the datasets are unrelated.
6) It's still listed as ongoing. Maybe they're checking back in with the infants? The required reporting deadline isn't until 7/15/2023.
Correct - glad you found that answer. So, obviously, that study could not have been used as a scientific basis for vax mandates in SEP 2021.