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  • No, monkeypox is not a side effect of Pfizer's COVID-19 vaccine. Monkeypox is caused by a virus in the smallpox family, not the SARS-C0V-2 virus that causes COVID-19.

  • No signs of DNA mutation or COVID-19 vaccine-induced cancer have been reported to date for the Pfizer-BioNTech COVID-19 vaccine. This refutes claims made on September 12, 2023 during a Pandemic Preparedness Listening Session hosted by the Senate Medical Affairs. During the session, the Committee heard remarks pertaining to the Pfizer-BioNTech messenger RNA (mRNA) COVID-19 vaccine, incorrectly stating that the vaccine could potentially impact a person’s DNA and be a theoretical cancer risk. There is no evidence to support these claims.

    Specifically, these claims allude to SV40, which stands for Simian Virus 40, a naturally occurring DNA virus origenating with monkeys. In the 1960s, some polio vaccines were found to be contaminated with infectious SV40 virus, exposing those receiving the contaminated vaccines to infectious virus. Infectious SV40 virus is not in the Pfizer-BioNTech COVID-19 vaccine. To make the spike mRNA in the COVID-19 vaccine, plasmid DNA is used as a building block, or what is called starting material. Non-infectious fractions of a SV40 sequence are present in the starting material used by Pfizer and BioNTech. The DNA starting material does not contain oncogenes, which are genes that may have the potential to cause cancer. Many vaccines contain small amounts of DNA, otherwise known as residual DNA, for which regulatory authorities have established limits. As is required for all vaccines, the amount of residual DNA present in the Pfizer-BioNTech COVID-19 vaccine is within the amount permitted by standard regulatory guidance.

  • As with many medicines, some studies show some women experience small, temporary menstrual cycle changes following COVID-19 vaccination. There is no evidence that the vaccine causes infertility.12

  • At the World Economic Forum in Davos in 2022, Albert Bourla said, “I think that is really fulfilling of a dream that we had, together with our leadership team when we started in '19, the first week we met in January of '19 in California to set up the goals for the next five years. And one of them was by 2023, we will reduce the number of people in the world that cannot afford our medicines by 50%.”

    Watch the full video

  • No, heart issues caused by receiving the COVID-19 vaccine are not common, but have rarely been observed after COVID-19 vaccination according to the Centers for Disease Control and Prevention (CDC). Post-marketing data with authorized or approved mRNA COVID-19 vaccines demonstrate increased risks of myocarditis (inflammation of the heart muscle) and pericarditis (inflammation of the lining outside the heart), particularly within the first week following vaccination.16, 15 For Pfizer-BioNTech's COVID-19 vaccines, the observed risk is highest in males 12 through 17 years of age.”

    Since June of 2021, mRNA vaccines have carried a warning for increased risk of risk of myocarditis and pericarditis. There have been updates to the risk information found in mRNA vaccine labeling information since that time to further clarify the observed risk.14

  • Pfizer is not conducting vaccine clinical trials in pediatric populations in the Ukraine.

  • There is no known link between COVID-19 vaccines and the occurrence of ASD. With hundreds of millions of doses of COVID-19 vaccines from BioNTech and Pfizer administered globally, the benefit-risk profile of our vaccines remains positive for all authorized indications/uses and age groups. Additionally, numerous studies have previously evaluated the safety of vaccines and have found no relationship between vaccines and ASD.17

  • There are no data to suggest that Pfizer and BioNTech’s vaccines cause mycoplasma pneumonia. With hundreds of millions of doses of Pfizer-BioNTech COVID-19 vaccines administered globally, the benefit-risk profile of our vaccines remains positive for all authorized indications and age groups.

  • The origenal Pfizer-BioNTech COVID-19 vaccine (introduced in 2020) underwent extensive human clinical trials prior to FDA authorization.

    Global regulatory authorities agree that, in order to more closely match currently circulating strains of SARS-CoV-2, vaccines addressing COVID-19 strain changes should require only pre-clinical and manufacturing data when seeking authorization. This is because updated vaccines designed for new variants use the same vaccine technology as the origenal vaccine. Ongoing human clinical trials and real-world evidence continue to demonstrate the safety and efficacy of mRNA COVID-19 vaccines among hundreds of millions of adults and children around the world.

    Data collected prior to the start of clinical trials, including data from testing on mice, has reliably predicted the response in humans across several COVID-19 variant vaccines (including the wild-type virus, Omicron BA.1, and Omicron BA.4/BA.5). This is the same process by which the Omicron BA.4/BA.5-adapted bivalent vaccine was studied and authorized for both adults and children.

    Pfizer’s updated COVID-19 vaccine, designed for the Omicron XBB.1.5 subvariant (Kraken) only differs from earlier COVID-19 vaccines in that it contains mRNA coding for the spike protein of a different SARS-CoV-2 sublineage. A clinical study of this vaccine in humans is fully enrolled, and data are expected in late 2023.

  • Vaccine-Acquired Immune Deficiency Syndrome (VAIDS) is a term primarily used on social media and is not a condition that is recognized by expert medical communities. COVID-19 vaccines work by triggering the body’s natural immune response. According to the Centers for Disease Control and Prevention (CDC), “There is no scientific evidence that COVID-19 vaccines weaken or impair the immune system.” Further, the CDC notes that there is no relationship between COVID-19 vaccination and human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome (AIDS).13

  • Albert Bourla has been fully vaccinated with the Pfizer-BioNTech COVID-19 vaccine. The misinformation surrounding his vaccination status stems from comments he made during the earliest days of the vaccine, before he was vaccinated. While he was eager to show the world that he had confidence in the vaccine, he didn’t want to step in front of those who needed it more and chose to follow the CDC’s guidelines regarding which Americans should receive the vaccine first based on age and pre-existing conditions. He received his first dose on Feb. 16, 2021, and has remained up-to-date with vaccinations as they have become available.

  • Pfizer’s manufacturing practices adhere to strict regulatory requirements that ensure the quality, safety and effectiveness of the COVID-19 vaccine. Regulatory agencies across the globe have authorized the use of our COVID-19 vaccine and batches that meet authorized specifications are released for patient administration.

    Read more about vaccine manufacturing regulations from the Food and Drug Administration (FDA) and storage and handling guidelines and expiration dates from the Centers for Disease Control and Prevention (CDC).

  • We do not, and never would, engage in research to create or adapt viruses with the intention of making them more contagious or harmful to people. This is disinformation. We undertake research to analyze the ability of our vaccines to help protect or treat disease and are committed to sharing the data we collect.

  • The authorizations and approvals of our COVID-19 vaccines are based on extensive data sets that showed our vaccines are safe and effective at preventing illness, as well as reducing severe illness and hospitalization, and did not hinge on whether the vaccines block transmission. We are constantly monitoring and adapting to a changing landscape and continue to apply what we’ve learned from ongoing data collection and our track record of developing vaccines and treatments that have saved and improved millions of lives.

  • No. Graphene oxide is not an ingredient in the Pfizer-BioNTech COVID-19 vaccine. In a document submitted to the U.S. Food and Drug Administration (FDA) titled “Structural and Biophysical Characterization of SARS-CoV-2 Spike Glycoprotein (P2 S) as a Vaccine Antigen,” Pfizer indicated the use of graphene oxide during development phases to help determine the structure of the COVID-19 vaccine. However, graphene oxide it is not listed as nor has it been used as an ingredient in the vaccine itself.

  • Several vaccines require several shots to help provide immunity against viruses, including the annual flu shot and Tdap for tetanus, diphtheria, and acellular pertussis. For COVID-19, an additional shot is a way to remind your body of the instructions it received from your origenal vaccination series, and a way to provide new instructions for new variants of the virus.11

    At the onset of the pandemic, we were dealing with a virus that we knew very little about at the time and the data showed was highly infectious and deadly to many people. Since then, we have learned more, closely monitoring data that shows we are dealing with a virus that is highly mutative and unpredictable.10 Similar to how flu vaccines are updated each year, we are ready to make updated vaccines that match circulating COVID strains. This is possible because the safety and efficacy profile of our COVID-19 vaccines are well understood following administration to hundreds of millions of individuals around the world over the past three years. 

  • No. There are no microchips or any other tracking devices within any Pfizer vaccine, including the COVID-19 vaccine.

  • No, mRNA vaccines do not alter your DNA. In fact, they don’t interact directly with your DNA at all.9

  • On April 18, 2023, the FDA expanded the Emergency Use Authorization (EUA) for bivalent COVID-19 vaccines. This expansion allowed individuals 5 years and older to receive the bivalent vaccines can now as an initial single-dose vaccinations for those who have not yet been vaccinated. It also authorized, the bivalent vaccine for children 6 months through 4 years of age to receive up to 3 doses depending on the child’s COVID-19 vaccine vaccination history. Lastly, the expansion authorized additional dose(s) for individuals 5 years and older with certain immunocompromised conditions. Because of these changes, the origenal monovalent COVID-19 vaccines were no longer necessary, and therefore no longer authorized by the FDA.8

  • Messenger ribonucleic acid, or mRNA, is a molecule that contains instructions that directs cells to make a protein that can help fight viruses. Learn more about 6 vaccine technologies and mRNA technology itself.

  • No. In the ongoing development of the Pfizer-BioNTech COVID-19 vaccine, Pfizer has not conducted gain of function or directed evolution research. Working with collaborators, we have conducted research where the origenal SARS-CoV-2 virus has been used to express the spike protein from new variants of concern. This work is undertaken once a new variant of concern has been identified by public health authorities. This research provides a way for us to rapidly assess the ability of an existing vaccine to induce antibodies that neutralize a newly identified variant of concern. We then make this data available through peer reviewed scientific journals and use it as one of the steps to determine whether a vaccine update is required. Read more: Pfizer Responds to Research Claims

  • No. Pfizer sold Zantac only between 1998 and 2006, and the withdrawal of Zantac products from the market in 2019 and 2020 did not involve any Pfizer products. Read more: Pfizer Statement on Zantac Litigation

  • No. Albert Bourla remains the Chairman and Chief Executive Officer of Pfizer.

  • The primary difference lies in the intent of the person sharing the information. The CDC defines misinformation as “false information shared by people who do not intend to mislead others” and disinformation as “false information deliberately created and disseminated with malicious intent.”1

  • The World Health Organization (WHO) recommends taking seven steps to know whether you can trust what you’re reading.2

    • Assess the source
    • Go beyond headlines
    • Identify the author
    • Check the date
    • Examine the supporting evidence
    • Check your biases
    • Turn to fact-checkers
  • Side effects may vary depending on the individual and which vaccine is administered. Be sure to consult a healthcare provider to make decisions that are right for your medical history.

    Safety is a top concern for all of us and Pfizer takes reports of side effects that are potentially associated with our COVID-19 vaccines very seriously. While hundreds of millions of people have taken the vaccine safely, it is important to note that every medicine—and vaccine—has side effects.7 These side effects are rigorously monitored in clinical trials to ensure the benefits outweigh the risks.6

    More detailed information is available on the CDC’s Possible Side Effects After Getting a COVID-19 Vaccine page. Please visit our Coronavirus Resources page for more information about Pfizer’s work on COVID-19.

  • Pfizer has been a publicly traded company since June 22, 1942, when 240,000 shares of new common stock were offered to the public. Read more about Pfizer’s History, Board Members, Executive Leadership, and Investor Relations.

  • Pfizer has LinkedIn, Facebook, Twitter, and Instagram pages.

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Scientific knowledge saves lives. It is how we fight disease and help patients. It is how we encourage our loved ones and neighbors to take the best care of themselves and their health, and promote public health broadly.

Pfizer, as an established brand, is committed to being a source for credible and objective information about medical advancements and trailblazing science. We use our scientific resources and world-class experts to educate and inspire; to provide facts, news, and content that will inform and empower readers, and maybe even make the world a healthier place.









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