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Our team is made of up writers, editors, advocates, and experts in various areas related to consumer safety and awareness. We strive daily to provide information that is informative, actionable, and timely.
ConsumerSafety.org provides legal connections for individuals suffering the consequences of problematic drugs, medical devices, consumer products, and hazardous conditions.
The black box warning was added in 2017 when regulators learned of an increased amputation risk with the diabetes medication. The warning removal stems from new data showing amputation risk at a lower level than previously reported. In 2017, the FDA used data from the CANVAS and CANVAS-R clinical trials to evaluate amputation risk. This means patients may have been unknowingly at an increased risk of FG for years before it was added to the Invokana label.
Bayer has proposed a new $2 billion settlement in its ongoing Roundup litigation battle. According to the proposal, the settlement class is composed of individuals meeting one of the criteria below: Previously diagnosed with NHL after Roundup exposure but have not yet filed a lawsuit Previously exposed to Roundup and develop NHL in the future The $2 billion fund would also cover other expenses, including: Creation of a science panel to assess medical evidence related to glyphosate and cancer Outreach efforts aimed at informing eligible individuals about the settlement With a maximum payout of $200,000 per claimant, the proposed settlement would cover only a small portion of NHL treatment costs.
Therefore 9/11 exposure may have put responders and survivors with these conditions at risk of severe COVID-19. On February 15, 2021, 9/11 responders and survivors became eligible for the COVID-19 vaccine in New York. How 9/11 Responders Can Secure a COVID-19 Vaccine Appointment in New York COVID-19 Vaccines for 9/11 Responders Outside New York State Individuals with 9/11 exposure should monitor their state COVID-19 vaccination pages.
May Produce Carcinogen in the Human Stomach Researchers from Memorial Sloan Kettering and Valisure, an online pharmacy, executed the study. Under conditions possible in the human stomach, a 300 mg Zantac tablet yielded 612,000 ng of NDMA. For reference, the U.S. Food and Drug Administration (FDA) has set a maximum daily exposure level of NDMA in drugs: 96 ng. Zantac generated less NDMA in other conditions also possible in the human stomach.