“Brightening” product claims continue to be flagged by FDA in warning letters, as well as statements about collagen production, cell regeneration and treatment of skin diseases. Medik8 marketer Ageless Aesthetics, Annemarie Gianni Skin Care and Be Green Bath & Body Founder Karen Roche are the latest warning recipients.
FDA issues a sharp reminder about unlawful structure/function and disease-treatment claims in the cosmetics sector, targeting three skin-care marketers with warning letters this month.
Issued July 18 to Ageless Aesthetics, Inc. and July 15 to Annemarie Gianni Skin Care LLC and Karen Roche, founder...
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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