Reye’s Syndrome is a disease which affects all organs of the body, but most lethally the liver and the brain. Reye’s Syndrome is a two-phase illness because it is almost always associated with a previous viral infection such as influenza, or chicken pox. Scientists do know that Reye’s Syndrome is not contagious and the cause is unknown. Reye’s Syndrome is often misdiagnosed as encephalitis, meningitis, diabetes, drug overdose, poisoning, sudden infant death syndrome, or a psychiatric illness.
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Epidemiological studies have linked the use of aspirin (a salicylate) to an increased risk of Reye’s Syndrome in children and teens, particularly when used to treat chickenpox, flu-like illnesses, colds, and similar conditions.
Avoiding aspirin (and products containing aspirin) in children and teens under 19 years of age is strongly recommended during viral illnesses and fevers, unless otherwise recommended by a physician. While Reye’s Syndrome may develop without the use of Aspirin, the risk is lower if aspirin is avoided in children and teens.
Read More for more information on other names for Aspirin and Aspirin-containing ingredients, and the particular risk to teens.
The National Reye’s Syndrome Foundation is a registered 501(c)(3) nonprofit organization dedicated to public education on health risks associated with aspirin use, including its link to Reye’s Syndrome. The information provided on our website, publications, and outreach materials is for educational purposes only and should not be considered medical advice. Always consult a qualified healthcare professional before making any medical decisions regarding aspirin or other medications. While we strive for accuracy, we do not guarantee the completeness or reliability of the information presented. The National Reye’s Syndrome Foundation does not endorse nor promote any specific treatments, products, or pharmaceutical companies.
For any medical concerns, please seek guidance from a licensed healthcare provider.
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