READ MORE: Pfizer has agreed to settle more than 10,000 lawsuits alleging it it of hiding the cancer risks of its heartburn drug Zantac.
Pfizer was the primary manufacturer of Zantac from 1998 to 2006, when several suits claim it should have known that the drug was contaminated with NDMA. NDMA is a chemical byproduct of many industrial manufacturing processes, including the production of rocket fuel. Since the drug was pulled and reformulated, thousands of lawsuits began piling up in federal and state courts against Pfizer, GSK, Sanofi and Boehringer Ingelheim, who have all owned the rights to the medication.
Health Pfizer FDA Cancer
We have summarized this news so that you can read it quickly. If you are interested in the news, you can read the full text here. Read more:
United Kingdom Latest News, United Kingdom Headlines
Similar News:You can also read news stories similar to this one that we have collected from other news sources.
Amgen plows ahead with costly, highly toxic cancer dosing despite FDA challengeWhen doctors began using the drug sotorasib in 2021 with high expectations for its innovative approach to attacking lung cancer, retired medical technician Don Crosslin was an early beneficiary.
Source: NewsMedical - 🏆 19. / 71 Read more »
FDA announce urgent recall of popular candy brand over salmonella riskIowa-based Palmer Candy Company has recalled its 'White Coated Confectionary items' due to potential salmonella contamination. The products were sold in stores like Walmart.
Source: DailyMailUK - 🏆 7. / 90 Read more »
New research reports on financial entanglements between FDA chiefs and the drug industryAn investigation published by The BMJ today raises concerns about financial entanglements between US Food and Drug Administration (FDA) chiefs and the drug and medical device companies they are responsible for regulating.
Source: medical_xpress - 🏆 101. / 51 Read more »
FDA brings lab tests under federal oversight in bid to improve accuracy and safetyMakers of medical tests that have long escaped government oversight will have about four years to show that their new offerings deliver accurate results, under a government rule vigorously opposed by the testing industry.
Source: medical_xpress - 🏆 101. / 51 Read more »
FDA-approved surgical robots trend toward autonomy, study findsA systematic review in npj Digital Medicine categorizes FDA-approved surgical robots by their levels of autonomy, highlighting a need for standardized definitions and greater regulatory clarity as these systems evolve towards higher autonomy.
Source: NewsMedical - 🏆 19. / 71 Read more »
First FDA-approved cellular therapy for metastatic melanoma available in South FloridaPatients in South Florida with metastatic melanoma will soon have access to the first cellular therapy for this advanced form of skin cancer, following its recent approval by the Food and Drug Administration (FDA).
Source: NewsMedical - 🏆 19. / 71 Read more »