Johnson & Johnson has agreed to settle with 43 state attorneys general over products that previously contained talc, planning to pay $700m in four payments through 2027. The settlement is not an admission of guilt, and J&J stands by the safety of the products in question, which it no longer markets with talc.
Johnson & Johnson will settle with a consortium of 43 state attorneys general to the tune of $700m to resolve allegations related to the marketing of its Johnson’s Baby Powder and Johnson’s Shower to Shower products, which used to contain talc.
The New Brunswick, NJ-based company – which has been embroiled in lawsuits for decades alleging that talc in its products...
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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