Health Canada and Canada’s environmental agency issued a draft screening assessment Dec. 8 identifying talc as potentially hazardous to consumers when used in cosmetic powders that may be inhaled or products applied to female genitals. Finalization of the assessment in its current form would trigger risk management actions.
Exposure to cosmetic-grade talc through female genital dusting or inhalation during powder product application may pose health risks, according to Canadian regulatory authorities.
Health Canada and Environment and Climate Change Canada published those tentative conclusions Dec. 8 in the form of a
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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