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div class = "card text-center" > < div class = "card-header" > < ul class = "nav nav-pills card-header-pills" > < li class = "nav-item" > < a class = "nav-link active" href = "#" >Active < li class = "nav-item" > < a class = "nav-link" href = "#" >Link < li class = "nav-item" > < a class = "nav-link disabled" href = "#" tabindex = "-1" aria-disabled = "true" >Disabled < div class = "card-body" > < h5 class = "card-title" >Special title treatment < p class = "card-text" >With supporting text below as a natural lead-in to additional content. < a href = "#" class = "btn btn-primary" >Go somewhere Images The MHRA is playing an active role in responding to the coronavirus pandemic. In relation to COVID-19 vaccines, the MHRA has authorised their supply following a rigorous review of their safety, quality and efficacy; however, as part of its statutory functions, the MHRA is responsible for monitoring all vaccines on an ongoing basis to ensure their benefits continue to outweigh any risks. This is a requirement for all authorised medicines and vaccines in the UK. This monitoring strategy is continuous, proactive and based on a wide range of information sources, with a dedicated team of scientists reviewing information daily to look for safety issues or unexpected, rare events. Speak to your doctor, pharmacist or to call NHS 111 if you are worried about your health as the MHRA is unable to provide medical advice. It is important that everyone submits a report to the Yellow Card scheme as soon as they suspect a side effect from a medicine or adverse incident associated with a medical device. This ensures that actions to reduce harm are based on the best available evidence and can improve safety for as many people as possible.
A number of detailed assessments of safety topics have been undertaken by the MHRA throughout the pandemic in relation to both monovalent and bivalent vaccines, and we have updated our advice on these topics accordingly. Overall, our advice remains that the benefits of the vaccines outweigh the risks in the majority of people. Further comments on use in specific populations and details on the specific safety topics can be found within the Section titled Analysis of data. The previous summary of COVID-19 Yellow Card reporting provides information on the monovalent vaccines used in the previous primary and initial booster campaign. Conclusion Cards are built with as little markup and styles as possible, but still manage to deliver a ton of control and customization. Built with flexbox, they offer easy alignment and mix well with other Bootstrap components. They have no margin by default, so use spacing utilities as needed. serious, medically significant or result in harm. Serious events are fatal, life-threatening, a congenital abnormality, disabling or incapacitating, or resulting in hospitalisation
A field safety corrective action (recall) by the manufacturer after several Yellow Card reports of mis-labelled femoral heads (medical device for the top part ball of the thigh bone in a hip replacement).
All vaccines and medicines have some side effects. These side effects need to be continuously balanced against the expected benefits in preventing illness. Up to 22 February 2023, the MHRA received 2,319 Yellow Card reports where the brand of vaccine was not specified by the reporter. Please note this may also include vaccines used in the primary and initial booster campaign where the brand of vaccine was not reported. Every report made to the MHRA Yellow Card scheme counts. Yellow Card reports are vital in building more knowledge and understanding about the potential risks of medicines and medical devices in clinical use and allows action to be taken to minimise harm to patients.Given the huge scale of the COVID-19 immunisation programme, with many millions of doses of vaccines administered over a relatively short time period, vigilance needs to be continuous, proactive and as near real-time as is possible. The importance of this is two-fold. First, we need to rapidly detect, confirm, and quantify any new risks and weigh these against the expected benefits. We can then take any necessary action to minimise risks to individuals. More information on the types of reports for these healthcare products can be found here. Aims of the scheme The Commission on Human Medicines (CHM) advises ministers on the safety, efficacy and quality of medicinal products. For COVID-19 vaccines, the CHM has a COVID-19 Vaccines Safety Surveillance Methodologies Expert Working Group and a COVID-19 Vaccines Benefit Risk Expert Working Group. Endocarditis
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