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Adverse events detailed for teen COVID-19 vaccination program

Medical Xpress

For adolescents aged 12 to 17 years, most reported adverse events following BNT162b2 vaccination are mild and self-limited, according to a study published online April 21 in Pediatrics.

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COVID-19 vaccination linked to fewer cardiac events

Medical Xpress

Analyzing the most extensive datasets in the United States, researchers from the Icahn School of Medicine at Mount Sinai have revealed that vaccination against COVID-19 is associated with fewer heart attacks, strokes, and other cardiovascular issues among people who were infected with SARS-CoV-2, the virus that causes COVID-19.

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COVID-19: No increased risks of adverse events found for vaccinated people

Medical Xpress

COVID-19 vaccines did not cause an increased risk of adverse events such as heart attack, stroke, cardiac arrest, myocarditis, pericarditis, and deep vein thrombosis. This was revealed by a study published in the journal Vaccines.

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Breaking: Healthcare Workers Experiencing Hope as Side Effect of COVID-19 Vaccine

GomerBlog

ATLANTA, GA – The most common side effect or adverse reaction healthcare workers are experiencing after the first dose of the Pfizer-BioNTech COVID-19 vaccine is hope, Gomerblog reports. ” VAERS was established in 1990 for the purpose of detecting any safety issues for vaccines licensed in the United States.

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New South Family Medicine and MedSpa Offers Next Level Care

New South Family Medicine and MedSpa

With the direct primary care model, your insurance is used for what it is intended to cover: catastrophic health events, hospitalizations, specialist care, imaging, and surgery. We follow ALL VACCINATION GUIDELINES set forth by the American Academy of Pediatrics and the American Academy of Family Medicine! Learn more.","robots":"index","keywords":"skin

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Anatomy of a Healthy Plate- Guest Blogger Rebecca Gray

New South Family Medicine and MedSpa

We follow ALL VACCINATION GUIDELINES set forth by the American Academy of Pediatrics and the American Academy of Family Medicine! Learn more.","robots":"index","keywords":"skin Learn more.","robots":"index","keywords":"skin

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FDA’s New RWE Guidance Provides Recommendations for Sponsors Conducting Non-Interventional Real-World Studies and Describes the Potential to Use RWE for Initial Approvals in One Limited Circumstance

FDA Law Blog

Postmarketing safety reporting obligations apply, but, if the sponsor is using only a subset of a larger dataset to conduct its analysis, FDA does not expect the sponsor to search the entire dataset regarding all uses of the product for adverse events that would meet reporting requirements.

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