Posted on 12/10/2020 1:11:53 PM PST by E. Pluribus Unum
You get Covid and you will not be given anything from most drs. I was told to alternate aspirin/Tylenol every 3 hrs. Nothing else.
Suspect is much to do about liability. Someone dies doing nothing ok, but god forbid they give you zinc/hqc/steriods
If we allowed people to be easily cured of this over blown illness, how would we maintain control?
Serious inquiry: Do you have credentials that qualify you to make those generalizations?
Ivermectin,
quercetin,
vit D,
vit B,
vit C,
zinc,
melatonin
Here’s the problem. Most Drs will not offer Covid patients treatments that work. It’s not a matter of xyz not having sufficient efficacy. They are not offered to patients. I don’t know if it’s liability, or what.
https://ivmmeta.com/ metadata from 23 studies detailing invermectin efficacy.
https://www.evms.edu/media/evms_public/departments/internal_medicine/EVMS_Critical_Care_COVID-19_Protocol.pdf This Covid protocol has been out in public from the beginning.
I saw something about Lactoferrin the other day too.
Steroids, eh?
So this is why COVID seems to have spared all the WWE professional wrestlers!
I’m with you and I’ve spreading the word here. I won’t touch this stuff. I tried to give our local Rep some benefit of a doubt, he’s a Christian guy, but the Alberta UCP and premier have lost their minds. They’ve been bought off, or are just extremely ignorant. Either way they’re complicit.
The public is being misinformed. Just this evening announcements are being made that the FDA is about to “approve” the Pfizer vaccine.
What they are going to approve is an Emergency Use Authorization (EUA).
FDA
Pfizer-BioNTech COVID-19 Vaccine
VRBPAC Briefing Document
“In the event an EUA is issued for this product, it would still be considered unapproved and it
would be under further investigation (under an Investigational New Drug Application) until it is
licensed under a Biologics License Application (BLA).
Licensure of a COVID-19 vaccine will be
based on review of additional manufacturing, efficacy, and safety data, providing greater
assurance of the comparability of licensed product to product tested in the clinical trials, greater
assurance of safety based on larger numbers of vaccine recipients who have been followed for
a longer period of time,”
” Female study participants of childbearing potential were screened for pregnancy prior to each vaccination, with a positive test resulting in exclusion or discontinuation from study vaccination...Unsolicited AEs related to pregnancy include spontaneous abortion and retained products of conception, both in the placebo group. Pregnancy outcomes are otherwise unknown at this time.”
(FDA mandates three more 30 month studies- does not notify population that they will be guinea pigs)
“Sponsor studies will include completion of long-term follow-up from ongoing clinical trials as well
as the following three planned active surveillance studies. Of note, the Sponsor will submit plans
for a clinical study to assess safety and immunogenicity in pregnant women and has proposed
active surveillance studies designed to monitor vaccination during pregnancy within populations expected to receive the vaccine under EUA.
• Study Protocol Number C4591008. The Sponsor proposes to survey 20,000 U.S. health
care workers enrolled in the COVID-19 HERO registry as well as health care workers in
certain participating health care facilities about adverse events of special interest, and
other clinically significant events of interest after vaccination with the Pfizer-BioNTech
COVID-19 Vaccine. Incidence rates of these events in this cohort will be compared to
expected rates. The respondents would receive follow-up surveys for a 30-month period.
• Study Protocol Number C4591011. This study is an active safety surveillance evaluation
conducted within the Department of Defense Health System Databases using data
derived from electronic health records and medical service claims among covered U.S.
military and their families. Rates of safety events of interest in vaccinated participants
will be compared to unvaccinated comparators. The study will be conducted for 30
months.
• Study Protocol Number C4591012. This study is an active surveillance study for adverse
events of special interest and other clinically significant events associated with the
Pfizer-BioNTech COVID-19 Vaccine using the Veteran’s Health Administration electronic
medical record database. Vaccinated participants will be compared to unvaccinated
participants or to recipients of seasonal influenza vaccine. The study will be conducted
for 30 months.
Currently, the primary objective of all three proposed studies above is descriptive, and the list of
adverse events in the studies has not been finalized. FDA will provide feedback on these
studies after further review.
Following authorization of the vaccine, use in large numbers of individuals may reveal
additional, potentially less frequent and/or more serious adverse events not detected in the trial
safety population of nearly 44,000 participants over the period of follow up at this time. Active
and passive safety surveillance will continue during the post authorization period to detect new safety signals.
(The fact that this is an experimental vaccine should be disclosed to those who choose to take it and along with this admission of long term health risk.)
“...risk of vaccine-enhanced disease over time, potentially associated with waning immunity, remains unknown and needs to be evaluated further in ongoing clinical trials and in observational studies...”
Travis, really suggest Dr. Judy Mikovits recently published books. She really fills in the connections to retrovirus contaminated vaccines to the plethora of human suffering from vaccine induced illness.
So you believe govenment statistics.
Are you seeing a doctor for that?
Did you not read this? Ivermectin is the drug he is referencing, not steroids.
In a study of 1,200 health care workers, 400 received prophylactic treatment with this, 800 did not. 59% of the 800 got sick, NONE of the 400 did. That is remarkable. It is no wonder he says “nobody should be dying from this”.
Ivermectin bump.
Did the FDA approve thalidomide in the USA? I think that we were saved from that scourge. DES certainly caused a great deal of pain and sterilization in American women though.
These communists also said, “Just give us 2 weeks to flatten the curve! That’s it! We promise! NO lockdown or house arrests or martial law, just masks and social distancing!”
Where did you order ivermectin pills??
No. I did it this weekend.
Went to Pushhealth.com.
$65 dollars for the consult and the script was emailed to my preferred pharmacies.
MFO
>> Three of my sisters were sterile
That’s horrible.
In agreement re RNA.
I will see if that works from western Canada. Thanks.
It was MUCH worse for the Thalidomide victims. MUCH WORSE.
And this is [several versions of] a rushed 9-month RNA vaccine...
Click here to get an idea of what Thalidomide did.
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