TV News LIES

The Food and Drug Administration has approved a new generic version of the abortion pill mifepristone, prompting an outcry from conservatives who’ve been eager to restrict access to the medication.

The generic pill was approved in September, according to Evita Solutions, its manufacturer. It joins another generic pill that’s already on the market from GenBioPro, which was approved in 2019.

Andrew Dixon, a spokesperson for the Health and Human Services Department, noted that the FDA “has very limited discretion in deciding whether to approve a generic dMore...rug. By law, the Secretary of Health and Human Services must approve an application if it demonstrates that the generic drug is idMore...entical to the brand-name drug.”

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The US’s top public health agency was plunged into chaos on Wednesday after the Trump administration moved to oust its leader Susan Monarez, sworn in less than a month ago, as her lawyers said she would not resign and that she was being “targeted” for her pro-science stance.

Monarez, the director of the Centers for Disease Control and Prevention (CDC), was ousted on Wednesday evening, according to a statement from Department of Health and Human Services (HHS) that offered no explanation its decision.

“Susan Monarez is no longer director of the Centers for Disease Control and Prevention. We thank her for her dedicated service to the American people,” HHS said in an unsigned statement posted to social media.

Monarez, who was confirmed by the Senate just last month, appeared to have afoul of Robert F Kennedy Jr, the US health secretary, after she declined to support sweeping changes to US vaccine policies, according to reporting from the Washington Post and the New York Times.

On Wednesday eveninhttps://www.theguardian.com/us-news/2025/aug/27/cdc-director-susan-monarez-oustedg, her lawyers Mark Zaid and Abbe David Lowell told the Associated Press she had neither resigned nor been told she was fired.

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Sen. Richard Blumenthal (D-Conn.), a staunch vaccine supporter, said he was “heartbroken” after hearing parents recount how their once-healthy children were injured or killed by vaccines.

The parents’ testimony, delivered during Tuesday’s U.S. Senate hearing, “Voices of the Vaccine Injured,” did little to sway Blumenthal from his belief that vaccines are “safe and effective” — but the gut-wrenching stories did lead the senator to suggest he may be willing to look into the issue of whether pharmaceutical companies should be held liable for injuries caused by their products.

“Maybe we ought to look at this system,” said Blumenthal, referring to the National Childhood Vaccine Injury Act of 1986, which established a government compensation program for people injured by vaccines while granting legal immunity to vaccine makers.

Since 1986, the only recourse parents have had if their child was injured is to file a claim through the National Vaccine Injury Compensation Program (VICP) — a bureaucratic labyrinth that rejects nearly half of all claims.

Blumenthal, ranking member of the Permanent Subcommittee on Investigations, which held the hearing, said the parents’ testimony “makes me want to do something.”

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A group of ice cream makers that produce 90% of the nation’s ice cream and frozen dairy desserts are pledging to eliminate many artificial food dyes from their offerings by the end of 2027.

The announcement, less than a week before the National Ice Cream Day on July 20, was made by the International Dairy Foods Association, a trade group for dairy companies, in conjunction with Health Secretary Robert F. Kennedy Jr., who has championed the cause through his Make America Healthy Again platform.

Kennedy, who has long blamed chronic health problems, including obesity and heart disease, on the food industry, announced in April that eight artificial dyes will be phased out from medications and the nation's food supply by the end of 2026, including those found in candy, ice cream, soft drinks and jams.

The voluntary effort will eliminate the use of certified artificial colors Red 3, Red 40, Green 3, Blue 1, Blue 2, Yellow 5, and Yellow 6.

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Health Secretary Robert F. Kennedy Jr. has fired all 17 members of a committee that advises the federal government on vaccine safety and will replace them with new members, a move that the Trump administration's critics warned would create public distrust around the government's role in promoting public health.

At issue is the Advisory Committee for Immunization Practices, which makes recommendations on the safety, efficacy, and clinical need of vaccines to the Centers for Disease Control and Prevention. It comprises medical and public health experts who develop recommendations on the use of vaccines in the civilian population of the United States.

“Today we are prioritizing the restoration of public trust above any specific pro- or anti-vaccine agenda,” Kennedy Jr., who has a history of controversial views on vaccines, said on June 9 in announcing the overhaul. “The public must know that unbiased science—evaluated through a transparent process and insulated from conflicts of interest—guides the recommendations of our health agencies.”

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CT scans diagnose afflictions from tumors to kidney stones to life-threatening diseases and injuries, such as aneurysms and blood clots leading to stroke.

But the radiation emitted by this essential diagnostic tool may cause more harm than previously known and could eventually be responsible for roughly 5% of all cancers diagnosed in the U.S. in a single year, a new study finds.

"Medical imaging has potential benefits," said radiologist Dr. Rebecca Smith-Bindman, an epidemiology professor at the University of California, San Francisco, and lead author of the study published Monday in JAMA Internal Medicine. "It has potential harms as well, and it's really important to balance them."

Scientists long ago established that ionizing radiation emitted by computed tomography, or CT, scans increases cancer risk. But, since 2007, use of the imaging technique has surged 35%, the study says, due in part to growth in what Smith-Bindman and her colleagues call "low-value, potentially unnecessary imaging."

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