Plaintiff claims that she and other Californians purchased a NIVEA skin-firming lotion “that, but for Defendant’s illegal conduct, would not have been on the market” due to its alleged unapproved drug status. This is her second amended complaint against Beiersdorf, the first having been dismissed in August 2015.
Beiersdorf AG’s US division points to communications straight from FDA in its motion to dismiss a proposed class action alleging that a NIVEA “firming” lotion is an unapproved drug in violation of federal and California laws.
The case has notable implications for cosmetic marketers in a legal environment – particularly in California under its Unfair Competition...
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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