Record Number Of Fetal Deaths Following Covid
As of this most recent update in VAERS, we have now found 2,809 fetal deaths following COVID-19 shots injected into pregnant and child-bearing women for the past 11 months.
By way of contrast, using the exact same search parameters in VAERS, but excluding the COVID-19 shots, we found 2,168 fetal deaths following all FDA-approved vaccines for the past 30+ years. & VAX=FLU3& VAX=FLU4& VAX=FLUA3& VAX=FLUA4& VAX=FLUC3& VAX=FLUC4& VAX=FLUN& VAX=FLUN3& VAX=FLUN4& VAX=FLUR3& VAX=FLUR4& VAX=FLUX& VAX=FLUX& VAX=H5N1& VAX=LYME& VAX=MEA& VAX=MER& VAX=MM& VAX=MMR& VAX=MMRV& VAX=MEN& VAX=MENB& VAX=MNC& VAX=MNQ& VAX=MU& VAX=MUR& VAX=PER& VAX=PLAGUE& VAX=PNC& VAX=PNC10& VAX=PNC13& VAX=PPV& VAX=IPV& VAX=OPV& VAX=RAB& VAX=RV& VAX=RV1& VAX=RV5& VAX=RVX& VAX=RUB& VAX=VARZOS& VAX=SMALL& VAX=TTOX& VAX=BCG& VAX=TYP& VAX=VARCEL& VAX=YF& VAXTYPES= & VAXTYPES=Adenovirus& VAXTYPES=Anthrax& VAXTYPES=Cholera& VAXTYPES=Dengue& VAXTYPES=Diphtheria& VAXTYPES=Ebola& VAXTYPES=Encephalitis& VAXTYPES=HPV& VAXTYPES=Haemophilus& VAXTYPES=Hepatitis A& VAXTYPES=Hepatitis B& VAXTYPES=Influenza& VAXTYPES=Lyme& VAXTYPES=Measles& VAXTYPES=Meningitis& VAXTYPES=Mumps& VAXTYPES=Pertussis& VAXTYPES=Plague& VAXTYPES=Pneumonia& VAXTYPES=Polio& VAXTYPES=Rabies& VAXTYPES=Rotavirus& VAXTYPES=Rubella& VAXTYPES=Shingles& VAXTYPES=Smallpox& VAXTYPES=Tetanus& VAXTYPES=Tetanus & VAXTYPES=Tuberculosis& VAXTYPES=Typhoid& VAXTYPES=Varicella& VAXTYPES=Yellow Fever” rel=”nofollow”> Source.)
- FDA-approved vaccines: 72 fetal deaths per year
- COVID-19 EUA shots: 3064 fetal deaths per year
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Can Pregnant Women Get The Covid
Pregnant women were not included in the early COVID-19 vaccine studies, but some participants were either pregnant and did not know it or became pregnant during the course of the study. Likewise, tens of thousands of pregnant women have been immunized since the COVID-19 mRNA vaccines became available, and many of them are also being monitored through the CDCs V-safe program.
With data from thousands of these women now in hand, no concerns have been identified and the vaccine works. While pregnant women and their babies will continue to be monitored, the CDC recently changed its statement about COVID-19 vaccines for pregnant women to more clearly recommend these vaccines for pregnant women.
Two factors, in addition to the vaccine data, were important for informing vaccine recommendations for pregnant women:
- First, some pregnant women are at high risk for COVID-19 because of their jobs, such as healthcare workers, or existing health conditions.
- Second, pregnant women are more likely to be hospitalized and be admitted to the intensive care unit with COVID-19 than women of the same age who were infected but werent pregnant.
All pregnant women should keep these two important points in mind:
Q: How Can We Be So Sure About The Effectiveness Of The Pfizer
A: In a randomized, blinded clinical trial, participants are not aware of whether they received vaccine or placebo. Therefore, any mitigation efforts would have affected those who received vaccine and placebo equally. The relatively high infection rate among placebo recipients suggests that that any mitigation efforts among trial participants may not have been very effective.
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Can I Get The Covid
In the U.S., the CDC recommends waiting until COVID-19 symptoms go away and the individual is done isolating. However, they indicate that it is okay to get the COVID-19 vaccine shortly after recovering from the disease as long as the patient was not treated with antibody-based treatments .
Due to limited supplies of vaccine in some countries and the experience that people who recently had COVID-19 rarely get re-infected in the months immediately after recovery, some areas may be delaying vaccination of recently recovered individuals. As such, we recommend talking with your healthcare provider or health officials to see what the recommendations are in your area.
How Long Should I Wait To Get The Covid
You should speak with your doctor to determine whether the quantity of steroids that you are receiving is suppressing your immune system. If so, you should hold off on receiving vaccines until the effect of the steroids has worn off.
Find out more in this Parents PACK article, “Medications and COVID-19 Vaccines: What You Should Know.”
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What Should I Do If I Had The J& j Vaccine
If you had the J& J vaccine more than 3 weeks ago, you are extremely unlikely to experience either thrombosis with thrombocytopenia syndrome or Guillain-Barré syndrome .
If you had the J& J vaccine within the last 3 weeks, although the risk is low, you should still monitor yourself for unusual symptoms, including severe headache, severe abdominal pain, unexplained leg pain, or shortness of breath, which may result from TTS, or muscle weakness or paralysis, which may result from GBS. If you develop unusual symptoms, you should seek medical attention and be certain to tell the healthcare provider the date you received the J& J vaccine. For TTS, the physician can very quickly determine whether your problem is related to the vaccine by performing a simple complete blood count. If the platelet count is extremely low, the symptoms might be related to the vaccine. We would also recommend registering for v-safe, the CDCs vaccine monitoring system if you have not done so already.
Could The Mrna Vaccines From Pfizer And Moderna Cause The Same Clotting Problem As The J& j Vaccine Did
The Johnson & Johnson /Janssen COVID-19 vaccine is an adenovirus vector vaccine, which is different from the Pfizer and Moderna mRNA vaccines. At the time of the J& J/Janssen pause, more than 182 million doses of the mRNA vaccines had been administered and no cases of thrombosis with thrombocytopenia syndrome, or TTS, had been reported. Three people out of about 85 million doses of Moderna had blood clots, but they did not have low platelets. The number of blood clots experienced by those who got the Moderna vaccine would be expected based on the background rate of clotting in the general population.
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Getting Back To Normal
Next comes the challenge of manufacturing and distributing a vaccine. The full rollout may take months to get enough batches for the general public in the interim, authorities will prioritize distribution to those most at risk of contracting COVID-19 or those who are at highest risk of suffering the most severe effects of the illness, such as health care workers, older adults, adults with pre-existing conditions and essential workers.
As a new vaccine is distributed, the clinical trials will go on and data will continue to flow in about its long-term effectiveness and any potential safety issues. This will allow researchers and healthcare providers to adapt distribution as necessary.
Realistically, the general public likely wont have access to a vaccine until sometime this summer. Thats far later than Operation Warp Speeds initial goal of having 300 million doses available by January, but significantly faster than any other vaccine development effort to date.
Individuals who are interested in participating in the ongoing COVID-19 vaccine trialsincluding potential new vaccine candidates in future trialsmay sign up for the UChicago Medicine COVID-19 Vaccine Registry at covidvaccinestudies.uchicago.edu.
Adaptive Design For The Solidarity Trial
A clinical trial design in progress may be modified as an “adaptive design” if accumulating data in the trial provide early insights about positive or negative efficacy of the treatment. The WHO Solidarity trial of multiple vaccines in clinical studies during 2020, will apply adaptive design to rapidly alter trial parameters across all study sites as results emerge. Candidate vaccines may be added to the Solidarity trial as they become available if priority criteria are met, while vaccine candidates showing poor evidence of safety or efficacy compared to placebo or other vaccines will be dropped from the international trial.
Adaptive designs within ongoing Phase IIIII clinical trials on candidate vaccines may shorten trial durations and use fewer subjects, possibly expediting decisions for early termination or success, avoiding duplication of research efforts, and enhancing coordination of design changes for the Solidarity trial across its international locations.
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Albert Bourla And His Team Overcame Unproven Science And Manufacturing Bottlenecks Youre Asking For Too Much
It was a warm day in June and Pfizer was racing to develop a radical new vaccine based on a technology that had never been approved before. Mr. Bourla and his team were so optimistic they had committed hundreds of millions of dollars to build a global manufacturing network.
Mr. Bourla, speaking from his suburban New York home during one of Pfizers twice-weekly meetings on the project, told the team he wanted them to increase commercial production at least 10-fold.
Why cant we make more and why cant we make it sooner? Mr. Bourla demanded.
Mike McDermott, who oversees Pfizers global manufacturing network, pushed back. His team already was working furiously, he said.
Months from viral sequence selection to phase 1 study of vaccine
What were doing already is a miracle, he said he told Mr. Bourla. Youre asking for too much.
Even for jaded pharmaceutical scientists, what happened next was little short of miraculous. U.S. health regulators Friday night authorized the Covid-19 vaccine developed by Pfizer and its German partner BioNTech SE. The shot is already in U.K. use and will be the first given in the U.S., capping the fastest vaccine development ever in the West.
Pfizer CEO Albert Bourla at the companys offices in Cos Cob, Conn.
The Steps That Produced The Most Rapid Vaccine Rollout In History
Vaccine development is typically measured in years, not months. But as the COVID-19 pandemic rages on, scientists are racing the clockand breaking recordsto develop an immunization that provides protection against the virus.
The nations scientific community also faces another obstacle: convincing the public that the COVID-19 vaccine is safe, and how important it is to get a COVID-19 vaccination in the first place.
Even the most effective vaccine cant protect us or our loved ones if people are afraid to take it or will not take it, said Kathleen Mullane, director of infectious disease clinical trials at University of Chicago Medicine. We know things are moving faster than ever, but the nations scientific community has cooperated and collaborated in ways as never before and we are absolutely committed to making sure whatever is ultimately approved works and is safe. I am going to get vaccinated and am recommending vaccination for my family and friends because I believe in the safety and efficacy of these agents.
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What Side Effects Will My Child Experience From The Covid
Side effects in children 12 to 15 years of age were similar to what has been found in other age groups, including pain at the injection site, fatigue, headache, fever, chills, muscle pain, or joint pain. Likewise, other than injection site pain, side effects were more common after the second dose compared with the first dose. Most side effects were mild or moderate.
No one in the study experienced an allergic reaction following vaccination, but this age group is not less likely to experience such a reaction therefore, teenagers should remain at the site where the vaccine was given for 15 or 30 minutes based on their risk and history with severe allergic reactions using the same guidance offered for adults.
Recently, a small number of cases of myocarditis, or heart inflammation, have been identified in teens and young adults, particularly in the 4 days after receipt of the second dose of the vaccine. Chest pain, shortness of breath, or related symptoms should be reported to a healthcare provider, so that teens can be appropriately diagnosed and treated. Find out more in this video.
Find additional information:
Safety Monitoring After Vaccination
Even after emergency use authorization has been granted, Dr. Kenyon said safety data will continue to be collected, as participants are followed for up to 2 years. This adds another layer of reassurance as a person shifts from a trial to a real-life setting.
The trial is tens of thousands of participants, but for the vaccine program, you are getting into the millions. While unlikely, it may uncover any undetected toxicities that were not picked up by the trial.
The V-safe .
It is a smartphone-based system where you will be contacted actively by CDC to see how you are doing after being vaccinated and therefore pick up any adverse events that were not picked up in the trials, Dr. Kenyon explained.
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Building Facilities Ahead Of Time
The U.S. Federal government and others pre-built manufacturing facilities for several different vaccines before knowing if they would be approved. Typically, vaccine manufacturers wait until after phase 3 has been completed, and licensure is expected to spend so much money on these types of facilities.
We Also Have Evidence That Pfizer Knew About The Risk Of Their Covid
In May of this year , we published a report written by Bud Shaver of Abortion Free New Mexico based on a whistleblower who served on a COVID-19 task force and had found documents that Pfizer had submitted to the European Medicines Agency to authorize the shots in Europe, which included animal trials that showed there were serious birth defects occurring in rat specimens.
The Pfizer factsheets state that pregnant or breastfeeding women should discuss their options with their healthcare providers. Although the U.S. FDA has not released the full study details provided to them for approval of the emergency use authorization , the European Medicines Agency has.
The full study documents are available at www.ema.europa.eu.
According to the reproduction toxicity study on the Pfizer product, performed in pregnant rats: There was an increase of pre-implantation lossand,a very low incidence of gastroschisis, mouth/jaw malformations, right sided aortic arch, and cervical vertebrae abnormalities.
They claim that these pregnancy reductions are within normal histological ranges, however, they were consistently seen, and are likely statistically significant. Gastroschisis is where the intestines grow outside of the body.
Right-sided aortic arch means the heart has basically formed in the wrong direction .
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First Covid Vaccine Approved Full Year After Discovery Of Disease
Exactly a year later on 31 December 2020, not six months later as the graphic claims, the first vaccine against Covid-19 was approved for emergency use by the WHO. This was the vaccine developed by the pharmaceutical companies Pfizer and BioNTech.
The post claims the speed of its development is why the US Food and Drug Administration, or FDA, cant approve the Covid-19 vaccine Dis waarom die FDA nie die vaccine kan goedkeur nie. The post says nobody knows what the long-term consequences of the vaccine will be and dis waar die probleem lê, or thats where the problem lies.
The FDA is the organisation that ensures the safety and efficacy of medical drugs in the US.
The graphic was posted on 4 August 2021. On 23 August, the FDA fully approved the Pfizer-BioNTech vaccine for the US. The Moderna vaccine has been approved for emergency use by the FDA since December 2020 and the Johnson & Johnson vaccine since March 2021.
Regulatory authorities in other countries, such as the South African Health Products Regulatory Authority or Sahpra, have also evaluated and approved vaccines for their countries.
How Do Adenovirus Vector Vaccines Work
Adenovirus vector vaccines take advantage of a class of relatively harmless viruses, called adenoviruses. Some adenoviruses cause the common cold, but others can infect people without causing illness. To use these viruses for vaccine delivery, scientists choose types of adenovirus that do not cause illness and to which most people have not been exposed. They alter the virus by removing two of the genes that enable adenovirus to replicate in people, and they replace one of those genes with the one for the SARS-CoV-2 spike protein.
Find out more about adenovirus vaccines in this Vaccine Update article, Getting Familiar with COVID-19 Adenovirus-replication-deficient Vaccines.
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Johnson & Johnson Vaccine And Tts A Possible Rare Side Effect
A small number of people have developed a serious blood clot condition after they received the J& J vaccine. Nearly all reports of this problem have been in adult women younger than age 50. A review of all available data at this time shows that the J& J vaccines known and potential benefits outweigh its known and potential risks.
However, women younger than age 50 should be aware of this rare adverse event and should know that other COVID-19 vaccines are available.
For three weeks after receiving the J& J vaccine, you should watch for possible symptoms of a blood clot with low platelets called thrombosis with thrombocytopenia syndrome, or TTS. Although very rare and treatable when diagnosed in time, TTS is serious.
Get medical help immediately if you have any of these symptoms within 3 weeks of receiving the J& J coronavirus vaccine:
- Severe or persistent headaches or blurred vision
- Shortness of breath
- Easy bruising or tiny blood spots under the skin near the injection site
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Unlocking the coronavirus secrets
To back up a bit first, designing the vaccines began far earlier than the jabs-in-arms stage. It began with of SARS-CoV-2, the virus that causes COVID-19 . By early January 2020, that genetic blueprint was in hand and the first vaccines to test were ready just a few weeks later.
For some perspective, researchers first deciphered, or sequenced, the entire human genome over a span of almost 13 years, starting in 1990 and wrapping up in 2003 . Because of advances in computers, the same task now can take only hours.
Most crucially, researchers now had the genetic instructions for making the spike proteins that the virus uses to break into cells a key ingredient for making the vaccines. Jutting out from the virus surface, these spike proteins make an easy target for the immune system to recognize. Researchers knew to zero in on those proteins thanks to decades of work studying coronaviruses, including two that have caused other outbreaks of human diseases SARS and MERS. That work also identified the best form of the protein to use: a stable form just before the virus fuses with a cell its about to infect.
Finding a delivery system
Benefiting from past research
Getting fast results
Jumping the line
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