FDA

Texas Attorney General Ken Paxton has filed a groundbreaking lawsuit against Dr. Margaret Daley Carpenter, a New York physician, for prescribing abortion pills to a Texas woman who suffered severe complications, including heavy bleeding, landing her in the emergency room.

The FDA is considering a ban on Red 3, a dye in foods.

The U.S. Department of Agriculture (USDA) has ordered the nation's milk supply tested for bird flu. The December 6 guidance is designed to "facilitate comprehensive H5N1 surveillance of the nation’s milk supply and dairy herds," according to a press release.

The United States District Court for the Northern District of Texas has issued a decisive ruling against the Food and Drug Administration (FDA) in a significant case brought by the Public Health and Medical Professionals for Transparency (PHMPT).

Boycotts of a bovine methane-reduction supplement are underway over safety concerns. The protests come as Arla Foods, a major supplier of British supermarkets, launched a trial of Bovaer, the bovine supplement.

Earlier this year, the FDA approved a supplement for dairy cattle designed to reduce their methane emissions by 30%. The supplement, called Bovaer, was considered a "first-in-class methane-reducing feed ingredient," a press release says.

The Food and Drug Administration (FDA) has approved Merus NV’s therapy Bizengri, the first treatment targeting the NRG1 gene, offering new hope for patients with challenging forms of lung and pancreatic cancers.

President-elect Donald Trump’s transition team is unveiling the "Make America Healthy Again" (MAHA) initiative, spotlighting a lineup of bold reformers slated to lead the nation’s healthcare overhaul. Trump’s Cabinet picks are positioned to tackle bureaucracy, corruption, and America’s rising chronic disease rates, with a focus on transparency and competition.

Robert F. Kennedy Jr. aims to ban pharmaceutical advertising if confirmed as Secretary of the Department of Health and Human Services.

Senator Ron Johnson (R-WI) is planning to issue subpoenas to the Centers for Disease Control and Prevention (CDC), the Food and Drug Administration (FDA), and the Department of Health and Human Services (HHS) over data pertaining to the COVID-19 vaccine.