As recently reported by The Rose Sheet, FDA continues to investigate more than 21,000 adverse-event reports from users of WEN Cleansing Conditioners, marketed by Chaz Dean and Guthy-Renker, LLC. The agency published an alert July 19, noting that the cause of the AEs is still not known, and issued a call to consumers and health care providers for information that could help to fill in the blanks.
FDA is asking consumers who have suffered hair loss or other adverse reactions to WEN Cleansing Conditioners, as well as their doctors, to provide information to the agency to assist in its ongoing investigation.
In an alert issued July 19, the agency affirmed that its probe into the matter is ongoing, noting...
Devices authorized for marketing outside the US. Data derived from Citeline’s Meddevicetracker. Updated weekly.
PATIENT ACCESS TO UNAPPROVED MEDICAL PRODUCTS WOULD BE ALLOWED under legislation introduced by Rep. Peter DeFazio (D-Ore.) on July 12 and Sen. Tom Daschle (D-S.D.) on July 14. Called the Access to Medical Treatment Act, the legislation would allow health practitioners to administer unapproved drugs, devices, foods or dietary supplements to patients as long as there is no evidence the treatment causes harm and the patient is informed about the treatment and its possible side effects. DeFazio's bill is identified as HR 2019; Daschle's version will be assigned a bill number the week of July 17.
A look at new research on the cardiovascular effects of ADHD medications and what it means for clinical care. This article explores the latest clinical and epidemiological research on the cardiovascular effects of medications commonly prescribed for ADHD, examining potential heart-related risks, underlying mechanisms, and their implications for patient safety, clinical decision-making, and long-term treatment strategies across diverse age groups and risk profiles.
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