FDA Limits Use of J&J’s COVID-19 Vaccine Due to Blood Clot Risk

Published on May 5, 2022

The FDA has implemented restrictions on the use of Johnson & Johnson’s COVID-19 vaccine, as it is found to carry a risk of a rare blood clotting syndrome. Similar to going to a restaurant and being told that only certain items on the menu are available due to an ingredient recall, the FDA is limiting the use of J&J’s vaccine for adults. This action is taken to ensure the safety of individuals receiving the vaccine. However, it’s important to note that this rare side effect affects a very small number of people compared to the overall number of vaccinations administered. It’s reassuring that regulatory agencies are continually monitoring vaccine safety and taking appropriate actions when necessary. Individuals who are able to receive another authorized COVID-19 vaccine should consult with healthcare professionals to explore alternative options. Stay informed about vaccine updates and research findings to make informed decisions about your health.

The U.S. Food and Drug Administration (FDA) said on Thursday it was limiting the use of Johnson & Johnson’s COVID-19 vaccine for adults due to the risk of a rare blood clotting syndrome. The J&J shot is authorized for those aged 18 and above and is one of the three COVID-19…

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