How The Vaccines Damage The Body
Understanding the specifics of how the covid vaccines damages the body and then learning how the vaccines do not work against covid, illustrates that the pharmaceutical companies had no idea what they were doing and just needed to introduce vaccines to bring in billions of revenue. The way the vaccines damage the body is covered in the article How The Covid Vaccines Damage The Body.
In Johnson & Johnson Vaccine Clinical Trials
- 17% of participants identified as Black/African American
- 3.5% identified as Asian
- 8.4% identified as American Indian or Alaska Native
- 0.25% identified as Native Hawaiian or other Pacific Islander
- 8.6% identified with multiple races, or race was unknown or not reported
- 62% identified as White
In addition, about 45% of all participants identified as Hispanic/Latino.
Should People With Cancer Get A Specific Covid
As mentioned in Which COVID-19 vaccines are available?, the Pfizer-BioNTech and Moderna vaccines are mRNA vaccines, while the Johnson & Johnson vaccine is an adenovirus vaccine. The other main difference between them is that the initial series for the mRNA vaccines is given as two shots over 3 to 4 weeks, while the adenovirus vaccine is initially given as a single shot.
All three of the vaccines have been shown to be effective at lowering the risk of getting COVID-19, as well as the risk of severe illness, being hospitalized, or dying from the disease if you are infected.
At this time, the CDC prefers that people get one of the mRNA vaccines over the Johnson & Johnson vaccine. The mRNA vaccines are more readily available and dont appear to have the rare side effect of blood clots . For people who cant or dont want to get an mRNA vaccine, the CDC stresses that getting any COVID-19 vaccine, including the Johnson & Johnson vaccine, is better than being unvaccinated.
As new information about the different COVID-19 vaccines becomes available, its possible that the guidance about the different vaccines might change. For this reason, its important to talk with your cancer doctor about getting the vaccine.
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The Complete Lack Of Safety In Testing The Vaccines
This issue with the testing timetable is explained in the following quotation.
With mRNA-1273 and with all of the other COVID- 19 vaccines, clinical trials were rushed through in a very short period of time, which has meant that proper precautions to ensure their safety were not taken. Doctors 4 Covid Ethics
What Common Side Effects Might Children Experience After Being Vaccinated
A super appears on a pink background: COVID-19 vaccine questions
Cut to a new super on a white background with a pink border: What common side effects might children experience after being vaccinated?
Cut to a doctor in an office, then a super appears:
- Dr. Laura Sauvé
- BC Childrens Hospital
The doctor answers the question.
Dr. Laura Sauvé: Some children will have no reaction to their COVID-19 vaccine, while others may have some short-term side effects.
These side effects are usually mild and clear up on their own within hours or days.
Side effects experienced by children in the clinical trials were similar to those for youth 12 and older. Common side effects can include redness and soreness and swelling at the injection site, and your child may also feel chills, mild fever, headache, and joint and muscle aches in the first day or two after being vaccinated.
As with adults, your child will be asked to wait onsite for about 15 minutes after vaccination to watch for allergic reactions. Severe allergic reactions are very rare. They usually occur within minutes after a person receives the vaccine, and they are treatable.
Cut to a white screen with a pink border: Got questions?
Cut to a new white screen with a pink border:
The Canada wordmark with waving flag appears.
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The More The Person Is Vaccinated Or Boosted The Worse The Outcomes
The risk of the vaccines increases the more one takes them. This is explained in the following quotation.
A booster may provide a small incremental benefit in preventing severe COVID-19 infections however, the boosters are likely to cause many more severe adverse events. Looking at the data on secondary injections with the Moderna vaccine there are approximately 3 times as many Grade 3 or 4 adverse events after the second dose than after the first dose. However, this is not the case following the second dose of placebo in the Moderna placebo group. The net is that adding a boostershot is highly unlikely to induce a favorable health benefit that was missing with the first series of immunization. US COVID-19 Vaccines Proven to Cause More Harm than Good Based on Pivotal Clinical Trial Data Analyzed Using the Proper Scientific Endpoint, All Cause Severe Morbidity
Why Do Those That Become The Most Severely Ill Already Vaccinated
This is a concerning quotation.
A few days later, August 5, 2021, Dr. Kobi Haviv, director of the Herzog Hospital in Jerusalem, appeared on Channel 13 News, reporting that 95% of severely ill COVID-19 patients are fully vaccinated, and that they make up 85% to 90% of COVID-related hospitalizations overall. In Scotland, official data on hospitalizations and deaths show 87% of those who have died from COVID-19 in the third wave that began in early July were vaccinated. Global Research
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Commonly Reported Adverse Events
The most commonly reported adverse events with COVID-19 vaccines are expected vaccine side effects, such as headache, fatigue, muscle and joint pain, fever and chills and pain at the site of injection. The occurrence of these adverse events is consistent with what is already known about the vaccines from clinical trials.
What’s The Difference Between Fda Approval And Emergency Use Authorization
If a vaccine is fully approved by the FDA, it means that the information on the vaccine and its effects have been thoroughly reviewed, and the FDA has determined that the benefits outweigh the known and possible risks for the people it is meant to help.
In an EUA, the FDA allows the use of a vaccine or drug during a time of emergency, such as the current COVID-19 pandemic, when the available evidence shows the potential benefits outweigh the potential risks. Drugs and vaccines that have been given an EUA continue to be studied in clinical trials. An EUA is not the same as a full FDA approval, which requires a more thorough review of safety and effectiveness.
Even after a drug or vaccine has been given full approval, the FDA might continue to monitor it for unexpected side effects or for more information that might be helpful to know. For example, it is not yet clear how likely it is that someone who gets one of the vaccines could still spread the virus to others. This is still being studied, as are any possible long-term effects of the vaccines. Researchers are also still trying to determine how long the vaccines will provide protection against the virus.
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Mrna Allergic Reactions And Future Doses
Its possible for most people who experienced an allergic reaction to a COVID-19 vaccine to safely receive future doses of that same vaccine. This includes with an mRNA vaccine.
The National Advisory Committee on Immunization has recommendations for people who experienced a severe immediate allergic reaction after a first dose of an mRNA COVID-19 vaccine. People with a history of a severe immediate allergic reaction after a first dose of an mRNA COVID-19 vaccine should:
- consult with an allergist or another appropriate health care provider before receiving future doses of an mRNA COVID-19 vaccine
- receive future doses of an mRNA COVID-19 vaccine in a controlled setting with someone who is experienced in managing anaphylaxis
- be observed for at least 30 minutes after vaccination
- the normal observation period for people who havent experienced a severe immediate allergic reaction after vaccination is 15 minutes
If you know youre allergic to a component of an mRNA COVID-19 vaccine, consult with an allergist or your health care provider. It may still be possible for you to receive these vaccines.
Everyone Should Still Get Vaccinated
While the J& J vaccine pause has been lifted, some people might still be worried. But the United States has authorized use of two other safe and highly effective COVID vaccines, which use a completely different platform, said Dr. Fryhofer. Pfizer and Moderna mRNA vaccines are completely different and more than 180 million doses of mRNA COVID vaccines have been administered.
Additionally, there have been no reports of cerebral venous sinus thrombosis combined with thrombocytopenia in patients who have received mRNA vaccines by Pfizer or Moderna, she said, emphasizing that this rare, but deadly combination of blood clots and low platelets has not been seen with Pfizer and Moderna mRNA COVID vaccines.
Fortunately, based on current projections, the supply of both of these mRNA vaccines is fairly high and looks stable for at least the near future, said Dr. Fryhofer, adding that we need to encourage our patients to get vaccinated. This is the only way we can end this pandemic.
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What Is An Emergency Use Authorization How Is What That Different Than Fda Approval
Creating a new vaccine can sometimes take years, but COVID-19 vaccines were developed and distributed quicky and safely through Emergency Use Authorization . EUA is faster than the traditional FDA-approval process while still thoroughly evaluating vaccine data, risks and benefits.
In order to use the EUA process, all vaccines still had to meet rigorous standards set by the FDA, carefully balancing the potential risks and benefits of the products based on the data currently available. Three vaccines Pfizer, Moderna, and Janssen have received Emergency Use Authorization from the federal Food and Drug Administration.
When the FDA approves a drug, like Pfizers COVID-19 vaccine, it means the agency has determined, based on substantial evidence, that the drug is effective for its intended use, and that the benefits far outweigh the risks.
Have Patients Sign Up For V
Once a patient does receive their first dose of a COVID-19 vaccine, Dr. Fryhofer recommends signing up for the V-safe vaccination health checker, which is a smartphone-based tool from the CDC.
They’ll text you every day and you can tell them what your symptoms are, because you’re going to share your experience with others and everyone can learn from your experience, said Dr. Fryhofer, adding that it is important to not only sign up for v-safe, but to also get that second dose.
The AMA has developed frequently-asked-questions documents on COVID-19 vaccination covering safety, allocation and distribution, administration and more. There are two FAQs, one designed to answer patients questions, and another to address physicians COVID-19 vaccine questions.
Watch this episode of the AMA webinar series, COVID-19: What physicians need to know, where Peter Marks, MD, PhD, discusses the Johnson & Johnson COVID-19 vaccine pause with AMA President Susan R. Bailey, MD.
To learn more about COVID-19 vaccine developments, visit our vaccine resource guide.
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Could The Vaccine Cause Issues If Im Getting A Mammogram
Getting a COVID-19 vaccine might result in swollen lymph nodes under the arm in which the injection was given.
Swollen lymph nodes under the arm might show up on a mammogram done to screen for breast cancer, which could cause concern and might lead to the need for further tests.
If youre scheduled for a mammogram soon after you get a COVID-19 vaccine, its important to tell your doctor when and in which arm you received the injection. Based on your situation, they can discuss with you if you should change your mammogram appointment. Do not delay your mammogram without speaking to your doctor first.
The Johnson & Johnson Vaccine And Blood Clots: What You Need To Know
In the minds of many, the halt of the Johnson & Johnson vaccine in April delivered doubt just as the mass COVID-19 vaccinations were making progress. There are three vaccines authorized for use in the United States, but Johnson & Johnsons was a particularly important one, partly because its one-shot dose made it seem as though we might achieve herd immunity faster. Then, the government recommended pausing the companys vaccine after six women who received it developed rare blood clotsand one woman died.
We spoke to Yale Medicine infectious diseases expert Jaimie Meyer, MD, MS, and Yale Medicine hematologist Robert Bona, MDthey shared insights about the pause and answered commonly asked questions.
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Why Did The Fda Question The Strength Of J& js Booster Data
Even though the FDA advisory panel unanimously recommended authorization of Johnson & Johnsons booster in October, it also questioned a test used in the trial to support its application for authorization. Regulators questioned the accuracy of a test called pseudovirus neutralization assay , which is used to measure antibodies, suggesting that the low-test sensitivity could have affected the results of the clinical trial.
The upshot, though, is that despite the concern for low sensitivity of the psVNA, the advisory panel still recommended the second dose, said Dr. Sude at the time. They feel that everyone who received a first dose should be given the option to optimize protection based on the best data available at the time.
Should Cancer Patients And Survivors Get The Vaccine
Many expert medical groups recommend that most people with cancer or a history of cancer get the COVID-19 vaccine once its available to them. This includes people who have already had COVID-19.
The main concern about getting the vaccine is not whether its safe for people with cancer, but about how effective it will be, especially in people with weakened immune systems. Some cancer treatments like chemotherapy , radiation, stem cell or bone marrow transplant, or immunotherapy can affect the immune system, which might make the vaccine less effective. People with certain types of cancers, like leukemias or lymphomas, can also have weakened immune systems which might make the vaccine less effective.
Although we dont have specific information yet on how effective the vaccines might be in people being treated for cancer, its possible that the vaccines might not be as effective in people with weakened immune systems as compared to people with healthy immune systems. Despite this, experts still recommend that most cancer patients get the vaccine because those with a fragile immune system are at risk for severe COVID-19 disease, so getting even some protection from the vaccine is better than not having any protection. For people with a weakened immune system who are fully vaccinated , the CDC also has recommendations on getting an additional dose of COVID-19 vaccine. See Should I get a COVID-19 vaccine booster?
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Lies About The Vaccines Only Staying In The Shoulder Or Injection Site
One of the lies told by pharmaceutical companies was that the vaccines would only stay in the injection site area and were therefore very safe.
This is disproven in the following quotation.
The mRNA component of the model vaccine was detected in multiple organs as soon as two hours after the injection, which indicates rapid onset of uptake into the bloodstream. The organs that accumulated the mRNA at levels higher than those found in the plasma included the eyes and the spleen. Doctors 4 Covid Ethics
The Mass Vaccination Is Clinical Trial
The entirely experimental nature of the vaccines is explained in the following quotation. As noted Dr. Lidiya Angelova in a recent Genuine Prospect article:
Many people are unaware that they are participating in the largest clinical trial test of our times. It is because World Health Organization, healthcare authorities, politicians, celebrities, and journalists promote the experimental medical treatments as safe and efficient while in fact these treatments are in early clinical research stage.
It means that there is not enough data for such claims and that the people who participate are test subject.
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Safety And Effectiveness Frequently Asked Questions
Comirnaty and Pfizer-BioNTech are actually the same vaccine. Before the Food and Drug Administration approves a vaccine, it’s known by the company that created it . Once the FDA granted approval, Pfizer chose a brand name for the vaccine .
In November 2021, Pfizer released an updated formula of the Comirnaty COVID-19 vaccine. The update allows providers to administer the vaccine without using a diluent. Providers can still use any remaining vials of the formulation for people 12 years and older. Children 5 to 11 years old may only get the pediatric formula of the vaccine.
For full approval, the FDA evaluates data over a longer period of time than for an emergency use authorization. For the vaccine to be given full approval, the data must show a high level of safety, effectiveness, and quality control in vaccine production. The purpose of emergency use authorization is to ensure that people can get lifesaving vaccines prior to a longer-term analysis of data. However, EUA still requires a very thorough review of clinical datajust over a shorter period of time.
Three vaccines are authorized for emergency use or fully approved by the U.S. Food and Drug Administration . These vaccines are currently offered in Washington state.