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With supporting text below as a natural lead-in to additional content. As of 22 February 2023, for the UK, 4,096 Yellow Cards have been reported for the bivalent COVID-19 Vaccine Pfizer/BioNTech, 5,108 for the bivalent COVID-19 Vaccine Moderna, 57 for the COVID-19 Vaccine Novavax and 2,319 have been reported where the brand of the vaccine was not specified (please note this may also include vaccines which were used in the primary and initial booster campaign where the brand was not reported). Shown below are image styles, blocks, text styles, and a list group—all wrapped in a fixed-width card.From 1 September 2022 to 22 February 2023, the MHRA received and analysed 4,096 UK Yellow Cards from people who have received the bivalent COVID-19 Vaccine Pfizer/BioNTech. For all of the original COVID-19 vaccines, detailed review of all reports has found that the overwhelming majority relate to injection-site reactions (sore arm for example) and generalised symptoms such as a ‘flu-like’ illness, headache, chills, fatigue (tiredness), nausea (feeling sick), fever, dizziness, weakness, aching muscles, and rapid heartbeat. It is therefore important that the suspected ADRs described in this report are not interpreted as being proven side effects of COVID-19 vaccines. The original monovalent Pfizer-BioNTech vaccine is recommended for eligible persons aged 5-11 years while the COVID-19 vaccine Novavax (Nuvaxovid) is recommended for those who cannot receive an mRNA vaccine. They may also be used to limit the number of times you see an advertisement and measure the effectiveness of advertising campaigns.

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div class = "card text-white bg-primary mb-3" style = "max-width: 18rem;" > < div class = "card-header" >Header < div class = "card-body" > < h5 class = "card-title" >Primary card title < p class = "card-text" >Some quick example text to build on the card title and make up the bulk of the card's content. The nature of reported suspected ADRs across all ages is broadly similar, although, as seen in the clinical trials and as is usually seen with other vaccines, they may be reported more frequently in younger adults. There is no current evidence that COVID-19 vaccination while breastfeeding causes any harm to breastfed children or affects the ability to breastfeed.Underlying or previously undiagnosed illness unrelated to vaccination can also be factors in such reports. The current advice of the Joint Committee on Vaccination and Immunisation (JCVI) is that the COVID-19 vaccines, including booster doses, should be offered to those who are pregnant as a clinical risk group in the COVID-19 vaccination programme and can be given at any stage in pregnancy. A list of the recognised adverse effects of COVID-19 vaccines is provided in the information for healthcare professionals and the recipient information which can be found on the Coronavirus Yellow Card reporting site.

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Similar to the classic UNO game, you have to match either the color or the number of the top card in the discard pile. Three COVID-19 vaccines - the monovalent COVID-19 Vaccine Pfizer/BioNTech, COVID-19 Vaccine AstraZeneca and monovalent COVID-19 Vaccine Moderna – were used in the primary and booster vaccination campaigns up to the end of August 2022. div class = "card" style = "width: 18rem;" > < div class = "card-body" > < h5 class = "card-title" >Card title < h6 class = "card-subtitle mb-2 text-muted" >Card subtitle < p class = "card-text" >Some quick example text to build on the card title and make up the bulk of the card's content. If other COVID symptoms are experienced or fever is high and lasts longer than two or three days, vaccine recipients should stay at home and arrange to have a test. div class = "row row-cols-1 row-cols-md-3 g-4" > < div class = "col" > < div class = "card" > < img src = ".div class = "card-body" > < h5 class = "card-title" >Card title < p class = "card-text" >This card has supporting text below as a natural lead-in to additional content. In addition to the specific safety topics summarised in this report, a range of other isolated events or series of reports of serious suspected ADRs have been reported. The symptoms reported for the children (high temperature, rash, diarrhoea, vomiting and general irritability) are common conditions in children of this age, so some of the effects reported may have occurred by coincidence. COVID-19 vaccine Novavax (Nuvaxovid), approved by the MHRA on 3 February 2022, and indicated for use in those aged 12 years and above is also being used as a booster dose in the small proportion of patients who are unable to receive mRNA vaccines.

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Using a combination of grid and utility classes, cards can be made horizontal in a mobile-friendly and responsive way. The previous summary of COVID-19 Yellow Card reporting provides MHRA assessment of safety topics relating to monovalent vaccines used in the previous primary and initial booster campaign. First, we need to rapidly detect, confirm, and quantify any new risks and weigh these against the expected benefits. Erik ten Hag has reached his lowest point yet at Manchester United… his team were PATHETIC in their 3-0.

The MHRA will continue to carefully review and monitor all reports submitted to us including those that cite a fatal outcome following COVID-19 vaccination.