FDA

Tylenol Criticizes Calls for Label Shifts

Tylenol manufacturer Kenvue Brands LLC sent a letter to the Food and Drug Administration, criticizing demands that the drug's label be changed to reflect greater safety warnings.

FDA Launches Fast-Track Program for New Drugs

The FDA announced the first round of pharmaceuticals that will receive expedited reviews under the Commissioner’s National Priority Voucher (CNPV) pilot program.

FDA Approves Abortion Pill

The Food and Drug Administration approved a generic abortion pill.

Walmart Removing Dyes from Products

Walmart announced that it will remove synthetic dyes from its products.

FDA Begins Label Changes for Tylenol

The Food and Drug Administration (FDA) announced that it has initiated the process of changing the labeling for Tylenol in light of President Trump's announcement that acetaminophen is linked to autism development when used during pregnancy.

Paracetamol Autism Claims UK Response Sparks Rebuttal

The British Labour government strongly rebuked President Donald Trump’s recent warning about a potential link between autism and the use of paracetamol during pregnancy. Health Secretary Wes Streeting dismissed the claim during a Tuesday morning appearance on ITV, advising the public to trust the National Health Service (NHS) and British medical professionals over the U.S. President.

Private Equity Hospital Takeovers Linked to Declining Care

Private equity ownership of hospitals in the United States is linked to declining patient care, rising health complications, and the stripping of community healthcare resources, according to a new report by former FDA Associate Commissioner Peter Pitts.

Deceptive Drug Ads Challenged Under New Crackdown

The Trump administration has moved to ban drug commercials on television in a new memorandum.

FDA to Revisit Hep B Vax for Infants

FDA Commissioner Dr. Marty Makary suggested that the agency will revisit whether infants should receive the Hepatitis B vaccine.

FDA Pulls COVID Vax Emergency Approval

Health and Human Services Secretary Robert F. Kennedy Jr. announced that the FDA revoked the emergency use authorization for the COVID-19 vaccine.

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