The Illinois Department of Public Health (IDPH), along with the Centers for Disease Control and Prevention (CDC), is warning patients and health care providers about the risk of procedures involving unproven and non-Food and Drug Administration (FDA) approved stem cell therapies.
After an investigation of several bacterial infections in patients following the use of stem cell products from the ReGen Series (distributed by Liveyon, LLC), an FDA investigation into the manufacturer, Genentech, found numerous deviations from established good practices and FDA guidelines, including screening stem cell donors for diseases such as HIV, hepatitis B, and hepatitis C infections.
Thus far, no bacterial infections occurring in Illinois residents following the use of these cells have been reported to IDPH. However, IDPH is advising patients who received these cells since 2017 to talk with their health care providers about the need to be tested for HIV, hepatitis B virus, hepatitis C virus, and possibly other blood-borne infections.
IDPH is providing information to clinics and health care providers, as well as notifying known clinics who may have received this product. IDPH requests that clinics notify patients who received these stem cells.
Potential risks related to unproven stem cell treatments include:
• Injection site reaction
• Failure of the cells to work as expected
• Growth of tumors
• Potential for contamination of the product
Currently, the only stem cell treatments approved by the FDA are products that treat certain cancers, blood disorders, and the immune system.
Some clinics in the U.S. are marketing stem cell therapies with claims that the cells will treat many conditions, ranging from normal aging to chronic pain.
If you are considering stem cell treatments, check to make sure the product you are considering is on the FDA’s approved list of stem cell treatments.