The NGO – and Gwyneth Paltrow – are rallying consumer support for a stronger FDA position on contaminant lead in cosmetics. The group is confident that innovation enabling lead-free lipsticks and other color cosmetics would follow an outright regulatory ban, but that optimism may not accord with reality.
The FDA’s recent recommendation that trace lead in cosmetics be capped at 10 parts per million did not sit well with the Environmental Working Group, which has launched an online petition urging the agency to “get lead out of cosmetics.”
The NGO will be lodging comments on FDA’s draft guidance, issued at the tail end of 2016, by the agency’s...
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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