Thalidomide.
Diethylstilbestrol (DES).
Vaccine-Caused-Polio.
[All FDA approved.]
Will those touting the certain safety of the [9-month-developed] Covid 19 novel experimental RNA vaccine agree to be held legally and financially liable for birth defects, retardation or sterility 10 or 20 years from now?
If not, they should STFU.
“Will those touting the certain safety of the [9-month-developed] Covid 19 novel experimental RNA vaccine agree to be held legally and financially liable for birth defects, retardation or sterility 10 or 20 years from now?”
The federal government financially insures against vaccine damages.
“Birth defects, retardation or sterility” are not likely problems. The most likely problems would be immune system related.
We are all supposed to keep wearing the masks and remain in our 6 foot distance even if you have gotten the shot and you have the card.
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...”
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.