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January 6th, 2021 
Awake Goy January 05, 2021
(Natural News) BUENOS AIRES (Sputnik) – A physician in Mexico who received the Pfizer vaccine against the COVID-19 coronavirus, was admitted to an intensive care unit with seizures, breathing difficulties and possible encephalomyelitis, the country’s Health Ministry said on Saturday.
(Article by Sputnik republished from InfoWars.com)
“The 32-year-old doctor who received the Pfizer COVID-19 vaccine was admitted to the intensive care unit […] after developing rashes, convulsions, muscle weakness and breathing difficulties within half an hour after vaccination,” the ministry said.
The cause of the adverse reaction, which occurred while the doctor was still within the observation area after his inoculation, are currently under investigation.
According to the ministry, the preliminary diagnosis is encephalomyelitis.
“The doctor is under observation and treatment by specialists in critical medicine to reduce the brain inflammation presented. Intensive specialized treatment based on steroids and anticonvulsants will continue to reduce the risk of sequelae”, Health Ministry stated.
The patient is said to have a history of allergic reactions to other medications, such as Trimethoprim with sulfamethoxazole, which can cause serious symptoms, particularly skin rashes, angioedema and anaphylactic reaction, or even death.
The Mexican Health Ministry outlined in a statement that, according to current scientific data on the Pfizer and BioNTech vaccine, “no person had previously developed encephalitis after the application of the vaccine.”
Bill Gates excited about RNA and DNA vaccines, 16% of people in trials had severe reactions.
Read more at: VaccineInjuryNews.com.
New vaccines: thousands of health impact events in first few days!
CDC FIGURES SUGGEST CATASTROPHE LOOMS
by Steve Cook
URGENT, URGENT , URGENT
Please see the very short videor by Dr Vernon Coleman at this link:
https://brandnewtube.com/v/haLXfJ
Please share it as widely as you can
The CDC report he refers to is at this link:
The figures he refers to are on page 6 of the report in a table entitled,”V-safe Active Surveillance for COVID-19 Vaccines”..
Please make a copy of the report and/or share it widely before the CDC take it down because the numbers are utterly damning.
I have kept a copy on my computer just in case and also copied the pdf and pasted it somewehat crudely following this article.
The numbers referred to by Dr Coleman are these:
By just the FOURTH day of people receiving the shot,
- 112, 807 people had received it.
- and 3150 had had a “Health Impact event”.
A Health Impact Event is defined by the CDC as:
“unable to perform normal daily activities, unable to work, required care from doctor or health care professional.”
Be aware that this is WITHIN FOUR OR FEWER DAYS of receiving the first shot.
We do yet know what how high the numbers will go in the medium or long term. The history of vaccines tells us that many adverse effects will only show up as time goes by. So many health impact events almost immediately spells a potential government/pharmaceutical-made catastrophe in the longer term the scope of which we cannot even begin to guess.
And bear in mind this is only the first shot. We are told that follow-up shots will be needed for the vaccine to “work”.
No doubt the government spin machine will go into overdrive in an effort to explain all this away but if it does please note the effort to cover its own ass rather than taking steps to prevent further harm to its own citizens.
These figures tell us that very nearly 3% of people had a reaction almost immediately that made them unable to perform normal daily activities, unable to work, and required care from a doctor or health care professional.
If the vax program goes ahead with the reckless abandon the gov desires, in short order we are going to see, say, ten million people vaccinated. If three percent experience a health impact event, we are looking at 30,000 people requiring medical attention WITHIN DAYS.
One can only guess at what that figure will be weeks, months or years from now and the burden this will place on the NHS – you know, the health service the gov swore blind it wanted to “save” from being overwhelmed.
As Dr Coleman points out in his video, this is an emergency and the vaccination program must be halted immediately before we are facing a catastrophe far worse than the fake one the government pretended it was “dealing with”.
Any politician, official, “expert”, pundit, reporter and so on who tries to cover this up and/or does not immediately act to bring this to a halt is responsible for the consequences of inflicting this vaccine on their fellow citizens.
NOTE: These numbers were recorded by the CDC on its website TEN DAYS AGO. So this has been known about for at least that long. Yet nothing was done by either the US or UK governments to halt the vax rollout or at least warn the citizenry of the degree of adverse health impacts being experienced so quickly. Instead they just kept right on encouraging the people to take the shot, swearing blind it was safe and so on.
Please share and forward this warning as widely and plentifully as you can.
Resources:
OLD MAN IN A CHAIR (DR COLEMAN SUPPORTERS GROUP ON FACEBOOK)
NURSES AGAINST LOCHDOWN FB GROUP
A copy-anbd-paste of the PDF:
Anaphylaxis Following m-RNA COVID-19
Vaccine Receipt
Thomas Clark, MD, MPH
December 19, 2020
ACIP COVID-19 Vaccines Work Group
December 8, 2020 – UK initiated vaccination with Pfizer-BioNTech
COVID-19 vaccine
December 9 – UK authorities confirmed 2 cases of anaphylaxis after
vaccination
Prescribing information for both Pfizer-BioNTech and Moderna COVID-19
vaccines contains information on anaphylaxis
– Severe allergic reaction (e.g., anaphylaxis) to any component of the vaccine is a
contraindication to vaccination
– Appropriate medical treatment used to manage immediate allergic reactions must
be immediately available in the event an acute anaphylactic reaction occurs
following administration of the vaccine
Anaphylaxis in UK Following COVID-19 Vaccination
2
ACIP considered anaphylaxis risk during deliberations on Pfizer-BioNTech
COVID-19 vaccine during December 11-12 meetings
December 12 – CDC published clinical considerations for use of PfizerBioNTech COVID-19 vaccine
– Included guidance on contraindications and precautions
(https://www.cdc.gov/vaccines/covid-19/info-by-product/pfizer/clinicalconsiderations.html#contraindications-precautions)
CDC Guidance on Anaphylaxis Following COVID-19
Vaccination
December 18*, 2020 – CDC has identified 6 case reports of anaphylaxis
following Pfizer-BioNTech vaccine meeting Brighton Collaboration criteria for
anaphylaxis
– Cases were Brighton Collaboration levels 1 or 2
– Additional case reports have been reviewed and determined not anaphylaxis
Cases occurred within recommended observation window and were
promptly treated
One case had a history of anaphylaxis following rabies vaccination
All suspect cases were notified through VAERS or CDC notification processes
These case reports are undergoing/will undergo clinical case review by CISA
December 19** – 272,001 doses of vaccine have been administered
Anaphylaxis in US Following COVID-19 Vaccination
*December 18, 2020 at 2300 hrs EST
**December 19, 2020 at 0945 hrs EST
Close coordination with FDA
Discussions with CISA investigators, NIH, Medicine and Healthcare
products Regulatory Agency (UK), Allergy/Immunology experts, and
other partners
Published Interim Considerations: Preparing for the Potential
Management of Anaphylaxis at COVID-19 Vaccination
Sites (https://www.cdc.gov/vaccines/covid-19/info-byproduct/pfizer/anaphylaxis-management.html)
CDC Actions Following Reports
V-safe Active Surveillance for COVID-19 Vaccines
Dec 14 Dec 15 Dec 16 Dec 17 Dec 18*
Registrants with recorded 1st dose 679 6,090 27,823 67,963 112,807
Health Impact Events** 3 50 373 1,476 3,150
Pregnancies at time of vaccination 5 29 103 286 514
*Dec 18, 5:30 pm EST
**unable to perform normal daily activities, unable to work, required care from doctor or health care professional
Post-authorization pharmacovigilance systems have detected and
confirmed 6 anaphylaxis cases following vaccination
– Notifications received have been timely
– Notifications ruled out suggests systems are sensitive
Reinforce measures to recognize, respond, and report anaphylaxis
Persons with anaphylaxis following COVID-19 vaccination should not
receive additional doses of COVID-19 vaccine
Consultation with allergy/immunology experts to provide guidance on
evaluation of persons following anaphylaxis to COVID-19 vaccine
CDC Assessment and Further Actions
For more information, contact CDC
1-800-CDC-INFO (232-4636)
TTY: 1-888-232-6348 http://www.cdc.gov
The findings and conclusions in this report are those of the authors and do not necessarily represent the
official position of the Centers for Disease Control and Prevention
First featured on UK Reloaded
Four volunteers immunized with Pfizer’s coronavirus vaccine developed Bell’s palsy; FDA denies jab caused it
December 18, 2020 Ramon Tomey
(Natural News) Four volunteers who were given Pfizer’s coronavirus vaccine in clinical trials developed facial paralysis. The U.S. Food and Drug Administration (FDA) reported that the four participants experienced Bell’s palsy, a rare condition in which one side of the face is temporarily paralyzed. While the FDA did not state that the vaccine directly caused the paralysis, it warned that doctors should watch out for the side effect and promised to observe cases closely.
The FDA revealed this side effect in a report about Pfizer’s vaccine, which was made in partnership with German firm BioNTech. The report was released days before the U.S. regulator was scheduled to review the pharmaceutical firm’s emergency use authorization.
According to the FDA, less than 0.5 percent of trial participants — including the four cases of Bell’s palsy — experienced serious side effects. One experienced facial weakness within three days after immunization, but was back to normal after a few days. Another participant developed Bell’s palsy nine days after receiving the jab, while two others experienced facial paralysis 37 and 48 days following vaccination. These three volunteers eventually recovered from Bell’s palsy after 10 to 21 days.
The National Institute for Neurological Disorders and Stroke defines Bell’s palsy as a form of temporary facial paralysis or weakness on one side of the face resulting from the dysfunction of the facial nerve, which is in charge of facial muscles. It generally affects only one side of the face but has been known to affect both sides in rare cases.
Most people who experience Bell’s palsy notice that one side of their face starts to droop and their facial muscles weaken. Some get headaches or experience pain around the jaw or ear of the paralyzed side. In other cases, people lose their sense of taste or become more sensitive to sound.
The exact cause of Bell’s palsy is unknown, but it usually goes away by itself. However, muscle weakness stemming from the condition may be permanent in some cases.
The U.S. and the U.K. approved the Pfizer/BioNTech vaccine for emergency use – despite the risks it may carry
Despite the risk of developing Bell’s palsy, the FDA authorized the Pfizer/BioNTech BNT162b2 vaccine for emergency use in the U.S. on Dec. 11. (Related: Pfizer’s vaccine studies are based on FRAUD and put lives in danger, warns former Pfizer vice president.)
In a statement, the U.S. vaccine regulator said it has “determined that the … vaccine has met the statutory criteria [for approval].” According to the FDA, there was more than enough data proving that BNT162b2 may be effective at preventing COVID-19. The agency also said that the potential risks associated with the vaccine do not outweigh its potential benefits based on the data presented, which supports the jab’s use in people 16 years old and above.
FDA Commissioner Dr. Stephen Hahn said that the emergency use authorization for the Pfizer/BioNTech jab “is a significant milestone in battling [the] devastating [Wuhan coronavirus] pandemic that has affected so many families in the U.S. and around the world.”
Prior to the FDA’s authorization, the United Kingdom gave BNT162b2 the go signal to be used for vaccination. Mass immunization for COVID-19 in the country commenced on Dec. 8. (Related: UK begins mass vaccination program with Pfizer, starting with the elderly and healthcare workers.)
The Wall Street Journal reported that two National Health Service (NHS) workers experienced anaphylactic reactions after receiving the Pfizer vaccine. Both workers were found to have a history of allergy and have been using adrenaline autoinjectors to deal with their allergic reactions.
As a result, the U.K.’s vaccine regulator Medicine and Healthcare products Regulatory Agency(MHRA) updated its warning and advised people who have a history of significant reaction to medicines, foods or vaccines to avoid immunization with the Pfizer/BioNTech COVID-19 jab. The U.K.’s health system previously warned against vaccinating pregnant and lactating womenwith the BNT162b2 jab as its effects on fertility are still unknown.
Meanwhile, the NHS has announced that it would make resuscitation facilities available at all times for vaccinations and that immunization should only be carried out in facilities where resuscitation measures are available.
VaccineInjuryNews.com has more on the negative effects of vaccines on human health.
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