Myth : Vaccines Have A Microchip That Will Track And Control An Individual
This conspiracy theory has been propagated by anti-vaxxers who believe that the American business magnate, investor, and philanthropist Bill Gates will implant microchips to track people’s movement, using the vaccine as the method of delivery. This is untrue and has been clarified by Gates in the media.
This myth gained traction when a video was shared on Facebook making false claims about the optional microchip on the syringe’s label of the COVID-19 vaccine. This microchip’s purpose is to confirm that the injectable and the vaccine are not counterfeit and haven’t expired. It will also confirm if the injection has been used. People commenting on the video appeared to have misinterpreted the technology as an injectable. But the microchip is part of the syringe label and not the injectable substance itself.
What If I’ve Already Had Covid
People will still be offered the jab even if they have had Covid-19 in the past.
That’s because natural immunity may not be long-lived and immunisation could offer more protection.
Guidance says there are no safety concerns about giving jabs to people with “long” Covid either. But people who are currently unwell with Covid-19 should not receive the vaccine until they have recovered.
Scary Reports Of Deaths Following Covid
You might have seen the headlines on social media.
COVID-19 Vaccine-Related Fatalities Exceed 6,000.
6,000% Increase in Reported Vaccine Deaths 1st Quarter 2021 Compared to 1st Quarter 2020.
No matter your vaccination status or your feelings about getting the shot, those headlines likely give you pause. Can those numbers be right?;
These and similar shocking claims are the latest examples of COVID-19 vaccine misinformation. And as with most misinformation, these statements get traction because they start with a kernel of truth in this case raw data from a reputable source.;
Health Care Workers Answer Questions About The Covid
Shaquita Bell, MD explains that the COVID vaccines went through rigorous testing to ensure safety.
This information is shared for educational purposes only and should not be used as a substitute for professional medical advice. The views expressed are those of the featured medical professional and reflect information available to that professional at time of filming. Always consult a health care provider for any personal health decisions.
Who Approves Vaccines Or Treatments
Approval is only given in the UK if the regulator is happy that a vaccine is safe and effective.
Checks continue after approval to make sure there are no further side effects or long-term risks.
Independent experts on the Joint Committee on Vaccination and Immunisation decide how best to use a vaccine and who should get it.
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Skewing The Science And Other Themes
Bigtree has critics. He âconsistently picks experts and data he likes rather than looking at a full picture,â Dorit Rubinstein Reiss, PhD, a professor of law at the University of California Hastings College of Law, said in the journal Elsevier.
She and a colleague watched weekly episodes of The Highwire with Del Bigtree from Jan. 30, 2020, to April 2, 2020. They identified six consistent themes and compared them to the anti-vaccine movement.
Anti-vaccine activists also skew the science by rejecting studies that do not fit their views and by latching onto studies and experts that support them, says Reiss.
Bigtree also criticized the government for not funding more COVID-19 treatments like the antimalarial drug hydroxychloroquine, âwhich would have been the fastest way out of this.â
But results from the interim SOLIDARITY study, published last October, show that hydroxychloroquine and lopinavir/ritonavir had little to no reduction in the deaths of hospitalized COVID-19 patients, compared to the standard of care.
Bigtree claimed that that the global trial used a lethal dose of 2,400 milligrams total daily of hydroxychloroquine, rather than the standard dose clinicians use of 400-600 daily. The loading dose was 1,600 milligrams followed by 400 milligrams daily. The researchers said they chose the higher dose thatâs used to treat amoebic liver abscess, which is caused by an intestinal infection, rather than the lower dose for malaria.
What Exactly Is Mrna
Both the Pfizer-BioNTech and Moderna vaccines consist of a piece of genetic material called mRNA. Simply put, mRNA provides the cells of your body with instructions on how to make proteins.
In fact, mRNA occurs naturally in your body. Your cells use mRNA all the time to produce many types of proteins that are necessary for your health and well-being.
The mRNA in the COVID-19 vaccine contains instructions for making a viral protein called the spike protein. This is a protein thats found on the surface of the novel coronavirus. The virus uses it to attach to and enter a host cell in your body.
When you receive the vaccine, your body will recognize the spike protein as an invader. Because of this, it will produce antibodies to protect you against the coronaviruss spike protein.
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Myth: Getting The Covid
FACT:;The CDC continues to monitor the spread of COVID-19 and makes recommendations for wearing face masks, both for those who are fully vaccinated as well as those who are not fully vaccinated.
The CDC also recommends that masks and physical distancing are required when going to the doctors office, hospitals or long-term care facilities, including all Johns Hopkins hospitals, care centers and offices.
Johns Hopkins Medicines current mask safety guidelines have not changed, and we still require all individuals to wear masks inside all of our facilities.
Myth: Researchers Rushed The Development Of The Covid
FACT: Studies found that the two initial vaccines are both about 95% effective and reported no serious or life-threatening side effects. There are many reasons why the COVID-19 vaccines could be developed so quickly. Here are just a few:
- The COVID-19 vaccines from Pfizer/BioNTech and Moderna were created with a method that has been in development for years, so the companies could start the vaccine development process early in the pandemic.
- China isolated and shared genetic information about COVID-19 promptly, so scientists could start working on vaccines.
- The vaccine developers didnt skip any testing steps, but conducted some of the steps on an overlapping schedule to gather data faster.
- Vaccine projects had plenty of resources, as governments invested in research and/or paid for vaccines in advance.
- Some types of COVID-19 vaccines were created using messenger RNA , which allows a faster approach than the traditional way that vaccines are made.
- Social media helped companies find and engage study volunteers, and many were willing to help with COVID-19 vaccine research.
- Because COVID-19 is so contagious and widespread, it did not take long to see if the vaccine worked for the study volunteers who were vaccinated.
- Companies began making vaccines early in the process even before FDA authorization so some supplies were ready when authorization occurred.
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False: The Creator Of The Mrna Vaccine Says It’s Dangerous
One person spreading misinformation about COVID vaccinations claims to be the inventor of mRNA vaccines, like Pfizer’s and Moderna’s. Dr. Robert Malone has appeared on right-wing talk shows and conspiracy-theorist podcasts claiming that the mRNA vaccines cause spike proteins to spread in the body, leading cells to die. There’s no evidence for this.;
Malone’s Twitter bio suggests he’s the creator of mRNA vaccines, but this is misleading. In 1989, he wrote an important paper about developing mRNA vaccines, but this doesn’t make him their creator. Moreover, the vaccines developed by Pfizer and Moderna weren’t developed with Malone’s input.
The mRNA in the vaccines is a genetic sequence that gives instructions to cells to make the coronavirus spike protein. Once these spikes poke out of the cell, the body’s immune system goes to work creating antibodies to prevent an infection. This process doesn’t change a person’s DNA.
Teaching The Next Generation Of Health Professionals
At MU Health Care, we train future health professionals to provide advanced, patient-centered care. The students and faculty at University of Missouri stay up-to-date on the newest treatments and methods, getting the hands-on experience that will help them care for patients for years to come. Through the MU School of Medicine, MU Sinclair School of Nursing and MU School of Health Professions, we teach your future doctors, nurse practitioners, physician assistants, nurses and more to offer personalized care with confidence and compassion.
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Penn Researchers Weigh In On The Regulatory And Scientific Efforts To Track Covid
The mRNA vaccines for COVID-19, made by Pfizer/BioNTech and Moderna, are among the most powerful vaccines the world has ever seen. According to clinical trial data, they are more than 94% effective at preventing symptomatic disease, with real-world data bearing out that success. The other vaccine currently available in the U.S., Johnson & Johnsons Janssen vaccine, uses a viral vector and is also proving its strength. Its efficacy, which is better than seasonal flu shots, is 70% generally and even stronger against hospitalizations and death.
While these are new vaccines, the mRNA technologythe brainchild of the Perelman School of Medicines Drew Weissman and Katalin Karikóhas been tested in animals for years with excellent results. And the Pfizer/BioNTech and Moderna products have been used in broad circulation for half a year, with companies actively pursuing FDA approval.
Experts from Penn are keeping a close eye on the regulatory steps and reporting mechanisms involved in assessing vaccine safety. Others are conducting their own studies to evaluate the immune responses the vaccines inspire.
The outlook thus far seems promising, and rigorous research will continue to provide evidence that can safeguard public health and ensure trust in vaccines in the months and years to come.
False: There’s No Reason To Bother With The Vaccine When You Can Use Ivermectin
Ivermectin has yet to be proved to help treat COVID-19. The CDC, the FDA and the World Health Organization haven’t listed it as a treatment for the disease.;
The anti-parasitic drug became popular over the summer as a small number of doctors have claimed it improves the conditions of patients infected with COVID-19. But studies backing up their claims are either lacking in data, have a small number of participants or have yet to be peer-reviewed. Those studies that have been reviewed were found to have questionable methodology, ethical concerns and plagiarism.;
Some individuals insisting on taking ivermectin began using a version of the drug intended for animals. This resulted in an increased number of calls to statepoisoncenters due to side effects from the higher dosage contained in the animal version of the drug.;
You are not a horse. You are not a cow. Seriously, y’all. Stop it.
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How Safe Is The Vaccine
Millions of Americans have safely gotten vaccinated against COVID-19. However, because these vaccines are relatively new and the target of misinformation online, there may be apprehension about vaccine safety and efficacy.
Weve asked our Yale New Haven Health experts to help clarify what we know about the vaccines and their current safety profiles.
What Do We Know About The Safety Of The Available Vaccines
All of the data that are available indicate that the Pfizer, Moderna and Johnson & Johnson vaccines are safe. The Pfizer vaccine, which was granted full approval by the FDA, consists of genetic material called mRNA, which stimulates the immune system to protect against the virus. The vaccine material breaks down quickly after its absorbed into cells and it does not impact our genes. The Moderna vaccine works in the same way.
The COVID-19 vaccines are new, but RNA vaccines have been around for the better part of the last decade. Experts have been researching this method to develop vaccines against other illnesses including influenza, Ebola and the Zika virus. Those years of scientific development helped researchers get to the point where we are today.
The Johnson & Johnson vaccine is different from the Pfizer and Moderna vaccines and only requires a single dose.;
While all of the COVID-19 vaccines are still being studied, its important to note that they had to be approved by the FDA before they were cleared for use. After a multi-step process to approve a vaccine, the FDA, along with the CDC, will continue to monitor the safety of COVID-19 vaccines to rapidly detect safety problems if they exist.
Any time a new vaccine is presented to the FDA, its tested and reviewed thoroughly before approval, even if its for emergency use, said Thomas Balcezak, MD, chief medical officer for Yale New Haven Health.
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The Debate Over Covid
Better answers could arrive soon. Israel and some European countries are ahead of the United States in their version of booster plans. A study looking at the early days of Israels booster campaign, giving another dose of the Pfizer-BioNTech vaccine to people 60 or older, did not appear to turn up any new safety concerns. And statements from the companies about their small studies of boosters have indicated similar safety features to the earlier doses.
Since most issues tied to vaccination occur shortly after the shots are delivered, if there was a dramatic increase in risk in terms of the safety profile, wed start to see that soon, Slifka said.
Below, STAT outlines some of the side effects tied to the different vaccines and what experts are considering at this point.
The Risks Of Rushing A Covid
Telescoping testing time lines and approvals may expose all of us to unnecessary dangers
The excitement and enthusiasm for a COVID-19 vaccine by the end of 2020 is both palpable and understandable. We all hope for a rapid end to the pandemic and an effective vaccine would be a surefire solution. But there are risks that come with a fast-tracked vaccine delivered end of this year, not the least of which are the risks related to the safety of the vaccine itself.
Telescoping testing timelines and approvals may expose all of us to unnecessary dangers related to the vaccine. While preclinical trials to evaluate the potential safety and efficacy of vaccine candidates are likely to include tens of thousands of patients, it is still unclear whether that number will be large enough and a trial will last long enough to evaluate safety for a drug that would be administered to so many. The US alone plans to vaccinate hundreds of millions of people with the first successful candidate.;One serious adverse event per thousand of a vaccine given to 100 million people means harm to 100,000 otherwise healthy people.
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Should You Still Get The Vaccine If Youve Had Covid
You may be wondering if you still need to get the vaccine if youve already had COVID-19. The answer to this question is yes.
Scientists currently dont know how long natural immunity lasts after having COVID-19. Research on this topic is ongoing. A 2021 study of 188 people who had recovered from COVID-19 found markers of immunity up to 8 months after infection.
Instances of repeat infection have so far only been documented in
Risk Is Not Only A Number
One challenge public-health authorities face is putting risk into context without seeming to dismiss peoples worries, says Heidi Larson, an anthropologist at the London School of Hygiene & Tropical Medicine who specializes in risk and decision science. Even if authorities say the likelihood of a severe reaction is one in a million, she says, what people want an answer to is, What does that one in a million mean for me or someone in my family?
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It Took Scientists Significantly Less Time To Develop The Vaccine For Covid
When it comes to making a typical vaccine, no one is in a hurry, Dr. DSouza said.
Lets take the flu vaccine for example. Lets say theyre coming up with the next generation, a new type of flu vaccine, he said. There are currently flu vaccines available, so no company is in a hurry to get it out tomorrow because the old one is still working.
Enter the novel coronavirus, which caused COVID-19, upended lives and killed millions of people.
The reason why this moved so fast is because we had nothing, Dr. DSouza said. People were dying, and we really didnt have a choice but to complete the trials as quickly as we could without compromising any of the studies.
And with the need for a new vaccine came a desire to fund it.
In the U.S. alone, the government invested nearly $19 billion in vaccine research and development.
The initial input for this kind of research was very expensive, Dr. DSouza said. In fact, if most governments did not support the pharmaceutical companies, they would have had a very tough time getting all this done.
Takeaway: Imminent need and robust funding helped shorten the timeframe for vaccine development without compromising clinical trials.
After The Emergency Use Authorization
Part of the safety watch on these new biologics will happen through the regulatory process, which began with clinical trials. For COVID-19 vaccines, these trials happened much faster than is typical. But that doesnt mean any corners were cut, says Susan Ellenberg, a biostatistician at the Perelman School of Medicine.
Drug companies could enroll participants and collect the data they needed so quickly because the virus was everywhere. This isnt just a childhood disease or something rare, she says. It was a global problem with a huge amount of transmission and a huge number of people getting sick. In addition, the number of trial participants for these vaccines exceeded whats typical for vaccine trials.
Beyond that, to support Emergency Use Authorization for these vaccines, the FDA asked for a median of two months of follow-up safety data after participants completed the full vaccination regimen, a figure based on the fact that adverse events tend to appear in the first two months after vaccine administration.
Whats clear is that these vaccines are amazing. In terms of the immunological response they induce, theyre among the best vaccines weve studied. Penn Medicine immunologist John Wherry
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