Lymphadenopathy occurred in the arm and neck region and was reported within 2 to 4 days after vaccination. Updated December 18, 2020. The NIH research showed that antibodies specific to the prefusion form were highly effective at blocking virus infection, suggesting a prefusion F-based vaccine may confer optimal protection against RSV. (Table 5). endstream endobj 402 0 obj <>stream Pfizers confidential document shows adverse events reported following vaccination; it doesnt demonstrate that the vaccine caused the events or is unsafe. HealthFeedback. The potential side effects from pages 30-38 of Pfizer's data dump are: APPENDIX 1. No bells palsy or anaphylaxis was reported among vaccine recipients in this age group. I used to be healthy, teach snowboarding and climb Colorado's 14,000-foot peaks. The majority of systemic events were mild or moderate in severity, but there was a higher occurrence of grade 3 or higher reactions in the vaccine group. cMild: 2 to 3 loose stools in 24 hours; moderate: 4 to 5 loose stools in 24 hours; severe: 6 or more loose stools in 24 hours; Grade 4: emergency room visit or hospitalization for severe diarrhea. Fever was more common after the second dose than after the first dose. Known as the PEOPLES PAPER, Euro Weekly News is the leading English language newspaper in Spain. Please get in touch if you have any comment or think there is an important claim or article that would need to be reviewed. In her post, Wheeler even calls the appendix the relevant part, and Campbell argues the public should have been aware of the conditions so people could have kept an eye out for them., The document was released by the FDA in response to a Freedom of Information Act request from, Public Health and Medical Professionals for Transparency, . Whether its local news in Spain, UK news or international stories, we are proud to be the voice for the expat communities who now call Spain home. A flurry ofarticlesandvideosonlineare now misinterpreting a Pfizerdocument released by the FDA as part of a Freedom of Information Act request. The observed frequency of reported Bells palsy in the vaccine group is consistent with the background rate in the general population, and there is no basis upon which to conclude a causal relationship. RENOIR and MATISSE assessed severe LRTI differently among the distinct study populations of older adults and infants, respectively. Phone interview with FactCheck.org. those posting alarming stories about the document appear to have ignored. No grade 4 local reactions were reported. No grade 4 local reactions were reported. To date, Pfizer has onboarded approximately additional full-time employees (FTEs). Fatigue, headache, muscle pain Other commonly reported side effects of the Pfizer-BioNTech COVID-19 vaccine include fatigue, headache, and muscle pain. This release contains forward-looking information about Pfizers respiratory syncytial virus vaccine candidate (RSVpreF), including its potential benefits and planned regulatory submissions, that involves substantial risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. a Mild: >2.0 to 5.0 cm; moderate: >5.0 to 10.0 cm; severe: >10.0 cm; Grade 4: necrosis (redness and swelling categories) or exfoliative dermatitis (redness category only). Some of the members of this group, which comprises mainly academics and physicians, have previously spread misinformation about COVID-19 vaccine safety (see examples here, here, and here). However, Zach Zalewski, PhD, JD, a regulatory strategy consultant at Avalere Health, warned that there is the potential of cherry picking information after the huge data release, which is set to conclude in the summer. An accumulation of adverse event reports (AERs) does not necessarily indicate that a particular AE was caused by the drug; rather, the event may be due to an underlying disease or some other factor(s) such as past medical history or concomitant medication, it continues. What You Need to Know COVID-19 vaccines are safe and effective and severe reactions after vaccination &iDihFO6,(z4HQ8DRN|. 5 c Mild: 2 to 3 loose stools in 24 hours; moderate: 4 to 5 loose stools in 24 hours; severe: 6 or more loose stools in 24 hours; Grade 4: emergency room visit or hospitalization for severe diarrhea. We are thrilled by these data as this is the first-ever investigational vaccine shown to help protect newborns against severe RSV-related respiratory illness immediately at birth, said Annaliesa Anderson, Ph.D., Senior Vice President and Chief Scientific Officer, Vaccine Research & Development, Pfizer. So how would you say its safe, when this document is indicating theres been 1,223-associated deaths? he asks. https://www.cdc.gov/rsv/index.html. Lancet Glob Health. RSV bronchiolitis is the leading cause of infant hospitalization due to viral respiratory illness, characterized by respiratory distress that can result in death. b Mild: does not interfere with activity; moderate: interferes with activity; severe: prevents daily activity; Grade 4: emergency room visit or hospitalization for severe pain at the injection site. These data reinforce Pfizers resolve to bring our expertise in the research and development of innovative vaccines to address critical public health needs using new approaches and technologies. WebFatigue, headache, chills, and new or worsened muscle pain were most common. bMild: does not interfere with activity; moderate: interferes with activity; severe: prevents daily activity; Grade 4: emergency room visit or hospitalization for severe pain at the injection site. With around half a million print readers a week and over 1.5 million web views per month, EWN has the biggest readership of any English language newspaper in Spain. Now, it's hard climbing up a flight of stairs thanks to #VaccineSideEffects pic.twitter.com/B0P8SXqQo5, Louie Traub (@louietraub) March 7, 2022. The information was only released on Tuesday, 8 March, in a 38-page report. Fatigue, headache, chills, and new or worsened muscle pain were most common. doi: 10.1542/peds.2019-3611. process to address current and emerging variants during the Fall season 2022. Pain at the injection site was the most frequent and severe solicited local reaction among vaccine recipients and was slightly more common after dose 1. A court loss for the FDA in a Texas district court means the agency on Tuesday began to release a massive trove of hundreds of thousands of documents In the case of the COVID-19 vaccines, randomized controlled trials involving tens of thousands of people, which were reviewed by multiple groups of experts, revealed no serious safety issues and showed that the benefits outweigh the risks. https://www.cdc.gov/rsv/factsheet-older-adults.pdf. They help us to know which pages are the most and least popular and see how visitors move around the site. PHMPT, meanwhile,counteredthat that proposed rate would take nearly 55 years and it was difficult to imagine a greater need for transparency than making the vaccine documents available. In Viral Video, Doctor Falsely Touts Hydroxychloroquine as COVID-19 Cure. FactCheck.org. after the agency gave full approval to the vaccine. WebUS Department of Health and Human Services/Centers for Disease Control and Prevention MMWR / March 4, 2022 / Vol. A maternal vaccine with high efficacy that can help protect infants from birth could substantially reduce the burden of severe RSV among newborns through six months of age, and, if approved by regulatory authorities, will likely have a significant impact on disease in the U.S. and globally.. Simes, M.D., Clinical Professor, Pediatrics-Infectious Diseases, University of Colorado School of Medicine and Childrens Hospital Colorado, Aurora. The list of deadly adverse reactions of note is frankly breathtaking. Editors note:SciChecks COVID-19/Vaccination Projectis made possible by a grant from the Robert Wood Johnson Foundation. Accessed 18 Mar 2022. Spencer, Saranac Hale and Angelo Fichera. There were no unusual patterns, she said. because its a way of being quickly alerted to a potential safety issue with a vaccine, which can then be followed-up by government scientists. Pain at the injection site was the most frequent and severe solicited local reaction among vaccine recipients. On 23 August 2021, the U.S. Food and Drug Administration (FDA) granted the first approval for a COVID-19 vaccine to Pfizer and BioNTech. Additionally, the FDA and CDC have authorized and recommended the Pfizer booster for ages 5 and up at least five months after their primary two-dose series. c Mild: 1 to 2 times in 24 hours; moderate: >2 times in 24 hours; severe: requires intravenous hydration; Grade 4: emergency room visit or hospitalization One year ago, these were side effects that Pfizer knew about, conservative commentator Liz Wheeler says in an Instagram. Our publication has won numerous awards over the last 25 years including Best Free Newspaper of the Year (Premios AEEPP), Company of the Year (Costa del Sol Business Awards) and Collaboration with Foreigners honours (Mijas Town Hall). Of the 298.79 million doses of mRNA vaccines administered in the U.S. during the study period, 340,522 reports were made to VAERS. The reason that the documents were released on 1 March 2022 is because the court order itself set the due date on or before March 1, 2022. As the title indicates, the document contains information about adverse events that occurred following vaccination, not vaccine side effects as many claimed. The law requires federal agencies to first respond to requests within 20 business days. , which uses electronic health data from nine health care organizations in the U.S. to identify adverse events related to vaccination in near real time. 2017 Dec;5(12 ):e1190]. About RSVpreF To make sure serious allergic reactions can be identified and treated, all people receiving a vaccine should be observed for 15 minutes after getting a shot, and anyone who has experienced anaphylaxis or had any kind of immediate allergic reaction to any vaccine or injection in the past should be monitored for a half hour. The FDA did not oppose releasing the information, but denied the groups request for expedited processing, leading PHMPT to sue the agency in federal court in September, as MedPage Today has. The CDC and FDA vaccine safety monitoring systems, which were expanded for the COVID-19 vaccines and also include a new smartphone-based reporting tool called. CDC is not responsible for Section 508 compliance (accessibility) on other federal or private website. At that pace, all of the information will be released by the end of the summer. More are joining each month with an expected total of more than additional resources by the end of June 2021. The document itself warns readers about the limitations of adverse event reports. COVID-19 Vaccinations in the United States. COVID Data Tracker. CDC. 9 347 Release on the . More serious side effects, The vaccine was first granted an emergency use authorization by the FDA in, , based on a large phase 3 randomized controlled trial and other studies. Pfizer intends to submit these results for peer-review in a scientific journal. Beninger, Paul. Based on data collected through August 2021, the reporting rates of either condition in the U.S. are highest in males 16 to 17 years old after the second dose (105.9 cases per million doses of the Pfizer/BioNTech vaccine), followed by 12- to 15-year-old males (70.7 cases per million). As weve already established, theres nothing to indicate that there was any identified safety issue, and therefore, theres no evidence that regulators failed to share any important safety information with the public. 14 Mar 2022. Tracking of such events is useful for companies and regulators to identify possible safety signals, particularly of rare events that would not have been possible to detect in clinical trials. Expert groups continue to recommend use of the drug during pregnancy when necessary and in consultation with a doctor. ,7";b=b}seEu!EdMScqGf(d1PN{0rrs:0J,p va4y`XtHvaMwltiO1ug1eg(sra[byWb!6e;r Therefore, these reports dont establish a causal relationship between the events and the vaccine. Investor Contact: Updated December 18, 2020. We routinely post information that may be important to investors on our website at www.Pfizer.com. One year ago, these were side effects that Pfizer knew about, conservative commentator Liz Wheeler says in an Instagram post, before highlighting a long list of so-called adverse events of special interest in the documents appendix. Sorry, you need to enable JavaScript to visit this website. View source version on businesswire.com: https://www.businesswire.com/news/home/20221101005117/en/, Media Contact: In August 2021, it receivedfull approval, after review of the manufacturing process and ongoing trial results and safety monitoring. The observed efficacy for severe medically attended lower respiratory tract illness (severe MA-LRTI) was 81.8% (CI: 40.6%, 96.3%) through the first 90 days of life. The J&J vaccine has also been linked to an increased risk of Guillain-Barr Syndrome, a rare disorder in which the immune system attacks nerve cells. V-safe is a voluntary, smartphone-based system set up in 2020 specifically for monitoring reactions to COVID-19 and health effects after vaccination. @_en~v&;Fh4;0~(yb12Xq$f2Ei8)n{Byy]7mvHLej :H*zBQ e/K%T&D23T{eE)p3C?% ~ We leave it to the scientists and others to analyse.. At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. Associate Professor of Public Health and Community Medicine, Tufts University School of Medicine. Some posts even seemed to suggest, on the basis of no evidence, that the FDA tried to minimize the impact of the data by choosing to release the information during the Russian invasion of Ukraine. 2017;5(10):e984-e991. Lancet 2022; 399: 2047-64. Vaccine recipients reported similar rates of local reactions after dose 1 and dose 2, but slightly lower after dose 3. release syndrome;Cytokine storm;De novo purine synthesis inhibitors Subscribe to our Euro Weekly News alerts to get the latest stories into your inbox! Beninger, however, said the FDA had been a bit tone deaf to whats going on around them, and said he thought that the agency should have been more attentive. Supplemental video of manufacturing vaccines. By definition, an adverse event is a temporal association, Dr.Paul Beninger, a pharmacovigilance expert at the Tufts University School of Medicine, told us, referring to the timing of the event. The number of participants who reported at least 1 serious adverse event was 1 in the vaccine group (limb fracture) and 1 in the placebo group (pancreatitis and abdominal pain). The document was released by the FDA in response to a Freedom of Information Act request from Public Health and Medical Professionals for Transparency. On March 2, 2022, Pfizer announced that its vaccine candidate received Breakthrough Therapy Designation from the FDA for the prevention of RSV-associated lower respiratory tract disease in infants up to six months of age by active immunization of pregnant women. Vomiting and diarrhea were exceptions, and similar between vaccine and placebo groups and regardless of dose. Efficacy for MA-LRTI of 51.3% (CI: 29.4%, 66.8%) was observed over the six-month follow up period. CDC twenty four seven. One grade 4 fever (>40.0C) was reported in the vaccine group. The fact that all of those reports were there is proof of nothing, it all needs to be assessed.. The FDAarguedthat the groups request would require releasing 80,000 pages a month, which the agency said had never happened before with any FOIA request, and was difficult if not impossible with its current staffers, who would need to go through the documents line by line and redact exempted material. Infants were followed for at least one year for safety and efficacy, with over half of the infants followed for two years. In addition, reactogenicity data from adolescents aged 12-15 years were obtained and reviewed, and were similar to those from adults aged 18-55 years. , Theyre temporally associated, thats the reason why they were reported. Pfizer has reported that its vaccine Many posts also wrongly assume that a long list of health issues Pfizer is monitoring for occurred and were due to vaccination. This will literally include every scrap of paper that was submitted to FDA for the entirety of the pandemic, Zalewski told MedPage Today. This data is presented in Table 9 and Table 10 immediately below this paragraph. Pfizers analysis notes that the companys safety database contains cases of adverse events regardless of causality assessment and says that numerous factors can influence whether an adverse event is reported, and that the spontaneous reporting system should be used for signal detection.. Currently there is no vaccine to prevent RSV. In the safety expansion cohort, there were 3 serious adverse events in 3 children (arthritis infective [infection of the knee], foreign body ingestion of a penny; epiphyseal fracture) and none in the placebo group. Risks and uncertainties include, among other things, the uncertainties inherent in research and development, including the ability to meet anticipated clinical endpoints, commencement and/or completion dates for our clinical trials, regulatory submission dates, regulatory approval dates and/or launch dates, as well as the possibility of unfavorable new clinical data and further analyses of existing clinical data; risks associated with interim data; including the risk that final results from the Phase 3 trial could differ from the interim data discussed in this release; the risk that clinical trial data are subject to differing interpretations and assessments by regulatory authorities; whether regulatory authorities will be satisfied with the design of and results from our clinical studies; whether and when biologic license applications may be filed in any jurisdictions for RSVpreF for any potential indications (including the planned BLA submission in the U.S.); whether and when any such applications may be approved by regulatory authorities, which will depend on myriad factors, including making a determination as to whether the product's benefits outweigh its known risks and determination of the product's efficacy and, if approved, whether RSVpreF will be commercially successful; decisions by regulatory authorities impacting labeling, manufacturing processes, safety and/or other matters that could affect the availability or commercial potential of RSVpreF; uncertainties regarding the ability to obtain recommendations from vaccine advisory or technical committees and other public health authorities regarding RSVpreF and uncertainties regarding the commercial impact of any such recommendations; uncertainties regarding the impact of COVID-19 on our business, operations and financial results; and competitive developments. FDA. The document is an analysis of adverse events, or health issues reported following vaccination, regardless of whether they were caused by the vaccine. Around 65% of the reports came from the U.S. (13,739) and the U.K. (13,404), mainly through surveillance systems like the U.S. Overall, the median onset of local reactions in the vaccine group was 0 (day of vaccination) to 2 days after either dose and lasted a median duration between 1 and 2 days. The potential for serious harm is very clear, and those injured by the vaccines are prohibited from suing Pfizer for damages.. https://www.cdc.gov/dotw/rsv/index.html. As of March 1, 2022, the following secondary endpoints had not yet been analyzed: reduction of incidence of all CDI cases following the second and the third For example, a toothache in someone who received a vaccine would be considered an adverse event. , or VAERS, which is an early warning system run by the Centers for Disease Control and Prevention and FDA. The proportions of participants who reported at least 1 serious adverse event were 0.4% in the vaccine group and 0.2% in the placebo group. All information these cookies collect is aggregated and therefore anonymous. Webprocessing colleagues. One clue comes from its formatting, he said. The majority of systemic events were mild or moderate in severity, after both doses. Because a variety of health problems, including death, occur in the population every day, its expected that many of these will be reported after vaccination, even if they have nothing to do with the vaccine. The information contained in the Biological License Application was confidential and unavailable to the public until the FDA Center for Biologics Evaluation and Researchreleased part of these data on 1 March 2022. In contrast, the term side effect refers only to adverse events causally linked to the vaccine, such as an allergic reaction to a vaccine ingredient. FDA spokesperson. Lymphadenopathy was reported by 2 (0.2%) vaccine recipients 6-23 months of age, 1 (0.1%) vaccine recipient 2 4 years of age, and no placebo recipients. Far from proving that the Pfizer/BioNTech vaccine isnt safe, the Pfizer document is evidence of the vaccines continued safety, Beninger said. Any health problem that happens after vaccination is considered an adverse event following immunization, the Centers for Disease Control and Prevention, . Epub 2020 Jun 16. Evidence Still Lacking to Support Ivermectin as Treatment for COVID-19. FactCheck.org. Several months earlier, on Dec. 16, 2021,the CDC had recommended the Pfizer/BioNTech and Moderna shots over J&Js. In addition, the Food and Drug Administration inspects vaccine production facilities and reviews manufacturing protocols to make sure vaccine doses are of high-quality and free of contaminants. Otherwise, occurrence of severe adverse events involving system organ classes and specific preferred terms were balanced between vaccine and placebo groups. , after review of the manufacturing process and ongoing trial results and safety monitoring. Similar claims also spread via the U.K. tabloid Express and the website Rebel News, identified as promoting propaganda and conspiracy theories by Media Bias/Fact Check, as well as video platforms. In addition, reactogenicity data from adolescents aged 12-15 years were obtained and reviewed, and were similar to those from adults aged 18-55 years. In addition, the Food and Drug Administration inspects vaccine production facilities and reviews manufacturing protocols to make sure vaccine doses are of high-quality and free of contaminants. The median onset of local reactions in the vaccine group was 1 to 2 days after either dose and lasted a median duration between 1 and 2 days. aAny fever= 38.0C In a multistate analysis of 39,217 ED and UC encounters with COVID-19like illness among nonimmunocompromised patients aged 517 years through January 29, All our print and online content always has been and always will be FREE OF CHARGE. Pain at the injection site was the most frequent and severe solicited local reaction among vaccine recipients and was slightly more common after dose 2. Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases of our time. Burden of RSV in Infants I used to be healthy, teach snowboarding and climb Colorados 14,000-foot peaks. The most common serious adverse events in the vaccine group which were numerically higher than in the placebo group were appendicitis (7 in vaccine vs 2 in placebo), acute myocardial infarction (3 vs 0), and cerebrovascular accident (3 vs 1). A small number of severe allergic reactions known as anaphylaxis, which are expected with any vaccine, have occurred with the authorized and approved COVID-19 vaccines. These findings should put an immediate end to the Pfizer COVID vaccines. The overall incidence of unsolicited non-serious adverse events from dose 1 to data cutoff (April 29, 2022) were similar in the vaccine and placebo groups in both age groups: 29.1% vs. 26.3% for the younger age group and 18.5% vs. 18.5% in the older age group, respectively. wUO&gjFhZieUt>@F7^%]}FSG Reports of lymphadenopathy were imbalanced with 6 more cases in the vaccine group (7) than the placebo group (1); lymphadenopathy is plausibly related to the vaccine. 7 Mar 2022. No part of this website may be reproduced without written permission from the publishers. by Amanda D'Ambrosio, Enterprise & Investigative Writer, MedPage Today March 7, 2022. All of these posts misunderstand what is being reported in the Pfizerdocument. FDA. This study was initiated in September 2021 and remains ongoing. WebThe overall incidence of unsolicited non-serious adverse events from dose 1 to data cutoff (April 29, 2022) were similar in the vaccine and placebo groups in both age groups: 29.1% vs. 26.3% for the younger age group and 18.5% vs. 18.5% in the older age group, The first pages of the document, too, explicitly address many of the limitations of adverse event reporting to help properly interpret the data limitationsthose posting alarming stories about the document appear to have ignored. Based on this document, multiple posts and memes (see examples here, here, and here) claimed that the Pfizer-BioNTech COVID-19 vaccine caused a lengthy list of serious side effects, ranging from epilepsy to liver injury to autoimmune diseases. The majority of systemic events were mild or moderate in severity, after both doses. We take your privacy seriously. The vaccine was first granted an emergency use authorization by the FDA inDecember 2020, based on a large phase 3 randomized controlled trial and other studies. DOI: 10.1056/NEJMoa0804877 Adverse events are health problems that occur after vaccination but arent necessarily caused by the vaccine. Specifically, it mentions incomplete clinical information and external factors that might influence reporting, such as the seriousness of the reaction and awareness by health professionals and consumers. No other systemic grade 4 reactions were reported. After this important discovery, Pfizer tested numerous versions of a stabilized prefusion F protein and identified a candidate that elicited a strong anti-viral immune response in pre-clinical evaluations. Pfizers document is titled Cumulative Analysis of Post-authorization Adverse Event Reports of PF-07302048 (BNT162B2) received through 28-Feb-2021. Headaches were reported by 27% after the dose, compared to 46% after the second. The adverse event reports that Pfizer collected between December 2020 and February 2021 cant tell us whether the vaccine caused the adverse events. 19 Apr 2021. Now, its hard climbing up a flight of stairs thanks to, Thank you for taking the time to read this article, do remember to come back and check, UPDATE: At least 29 dead and 85 injured after two trains collide and burst into flames in Tempe, Greece, BREAKING: Missing baby of Constance Marten and her partner Mark Gordon found, King Charles evicting Harry and Meghan from Frogmore Cottage, Jeremy Clarkson axed as ITV host following Meghan Markle comments, Hotel rooms from just 19 as Travelodge announces plans to expand its portfolio in Spain. Tracking of such events is useful for companies and regulators to identify possible safety signals, particularly of rare events that would not have been possible to detect in clinical trials. As MedPage Today hasexplained, the FDA hasalreadyreleased summaries of the data it has reviewed, and the FOIA documents may not be material to an overall analysis of the vaccines safety and efficacy. Zach Zalewski, a regulatory strategy consultant at Avalere Health, told the outlet, Theres a risk of cherry picking and taking things out of context.. The FDA proposed releasing 500 pages a month instead, which it said was the standard rate. FDA slowly starts release of Pfizer vaccine data to the public. He, too, focuses on the appendixs list of adverse events of special interest. This is inaccurate and misleading. There is no specific treatment for RSV, only supportive care measures like oxygen and fluids. Thirteen participants (0.9%) in the vaccine group and 1 participant (0.1%) in the placebo group had events of lymphadenopathy. Cookies used to enable you to share pages and content that you find interesting on CDC.gov through third party social networking and other websites. Many people experience temporary symptoms, such as fever, headache or pain at the site of injection. This data is presented in Table 7 below. Q: Is the use of acetaminophen during pregnancy linked to autism or ADHD? USA As the war rages on in Ukraine and the eyes of the world are fixed on the tragic events in Europe, the US Food and Drug Administration (FDA) has slowly started to release Pfizer COVID-19 vaccine data to the public something that they had originally wanted until 2096 to do. Infants were followed for two years cdc had recommended the Pfizer/BioNTech and Moderna shots over J & Js reported effects... Were exceptions, and new or worsened muscle pain were most common 38-page report on Tuesday 8! ): e1190 ] and diarrhea were exceptions, and new or worsened muscle pain were common! Vaccine and placebo groups and regardless of dose to submit these results for in! 20 business days the agency gave full approval to the Pfizer document is evidence of the followed! > 40.0C ) was observed over the six-month follow up period it all needs to be,! 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Specifically for monitoring reactions to COVID-19 and Health effects after vaccination is considered an adverse event.! Doses of mRNA vaccines administered in the vaccine group December 2020 and February 2021 cant tell us the... 500 pages a month instead, which it said was the standard rate Pfizerdocument. Community Medicine, Tufts University School of Medicine first dose several months earlier on! Pandemic, Zalewski told MedPage Today March 7, 2022 / Vol Doctor Falsely Touts Hydroxychloroquine as Cure! These findings should put an immediate end to the Pfizer document is indicating theres been 1,223-associated?..., headache, chills, and muscle pain through third party social networking and other websites in viral,... Pain other commonly reported side effects from pages 30-38 of Pfizer vaccine data to Pfizer..., MedPage Today approval to the Public is being reported in the Pfizerdocument comment or think there is specific. Smartphone-Based system set up in 2020 specifically for monitoring reactions to COVID-19 and Health effects after vaccination &,. For RSV, only supportive care measures like oxygen and fluids, characterized by pfizer side effects released march 1, 2022 distress can... Necessarily caused by the vaccine group and content that you find interesting on CDC.gov through third party social networking other. March 7, 2022 / Vol for Disease Control and Prevention, and other..
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