Acetaminophen has been added to the list of over-the-counter painkillers that can cause rare but deadly skin reactions.
August 1, 2013 Medications can cause rare and dangerous allergic reactions. The FDA says that the popular painkiller acetaminophen can cause those reactions, too. The agency wants people to see a doctor quickly if they get a rash while using the drug.
July 11, 2013 Since 2007, the Food and Drug Administration has had the power to require drugmakers to continue studying the safety of their pills or other medicines as a condition for approving them in the first place. An analysis finds that many studies are behind schedule.
Don't get near that grill with the spray-on sunscreen.
July 5, 2013 Five people burst into flames last year after spray-on sunscreen ignited on their skin. The manufacturer has recalled those sprays, but the Food and Drug Administration says sprays can still pose a fire risk because they include flammable chemicals. So spray carefully, or opt for a shirt.
Federal authorities seized a bunch of websites belonging to online pharmacies that were allegedly breaking the law.
June 28, 2013 The Food and Drug Administration and the U.S. attorney's office in Colorado cracked down on more than 1,600 websites that the feds say are breaking the law in the way they're selling prescription drugs, some of them counterfeits.
Bad bug: The bacterium Clostridium difficile kills 14,000 people in the United States each year.
June 18, 2013 Fecal transplants are being used more often to treat life-threatening bacterial infections. But the Food and Drug Administration worried that the still-experimental procedure put patients at risk. Now it is dropping plans to restrict transplants after doctors and patients complained.
This brand may have a near-monopoly in emergency contraception.
June 13, 2013 Women and teenagers should soon be able to buy emergency contraception with no age restrictions, according to a federal district judge's memorandum. But the Obama administration's plan will put just one brand-name formulation of the "morning after" pill on store shelves.
These funny mustachioed fish are at the center of a farm bill fight in the House and Senate.
June 10, 2013 Inspecting seafood for safety hazards is currently the job of the Food and Drug Administration. But U.S. catfish producers want the Department of Agriculture involved, too. Critics say it's just a crackdown on foreign producers who are taking over the U.S. market.
May 22, 2013 Activists say the case against Wisconsin dairy farmer Vernon Hershberger is about raw milk — and much more. His supporters have turned the case into a rallying cry for personal food freedom and the rights of farmers and consumers to enter into private contracts without government intervention.
Microscopic bugs called cheese mites are responsible for giving Mimolette its distinctive rind and flavor.
Chris Waits/via Flickr
May 11, 2013 Microscopic bugs called cheese mites are responsible for the distinctive rind and flavor of the bright orange French cheese Mimolette. But now, the FDA has blocked more than a ton of Mimolette from entering the country, because the agency says the mites left on it make it unfit for consumption.
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U.S. District Judge Korman of New York is steamed about the administration's handling of the Plan B One-Step morning-after pill.
May 10, 2013 Iin denying the government's motion for a stay, U.S. District Court Judge Korman, who has overseen the case since 2005, also laid out several substantive problems with the situation that last week's approval by the Food and Drug Administration created.
The Plan B One-Step morning-after pill will now be available to women as young as 15 without a prescription.
April 30, 2013 Under the proposal, teenagers below 15 would now need a prescription to purchase the morning-after pill. That age was previously 17. The plan would also allow the product to be sold on retail shelves, rather than behind the pharmacy counters, with age to be verified by cashiers rather than pharmacy staff.
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Wrigley says its new Alert Energy Caffeine Gum gives consumers the power to control how much caffeine they get.
April 30, 2013 Wrigley's new caffeinated gum has raised eyebrows at the FDA, which is worried about the potential health impacts on children and teens.
Over the past several years, the FDA has deemed many dietary supplements to be "tainted" by unapproved drugs.
April 23, 2013 More than 200 dietary supplements have been recalled in recent years because they contain drugs that aren't listed on the label, an analysis finds. The ingredients are potentially harmful, researchers say.
Plan B is one of two emergency contraceptives available in the U.S.
April 5, 2013 The ruling could end a more than decade-long battle that has spanned two administrations. The decision overturns a controversial 2011 action by Secretary of Health and Human Services Kathleen Sebelius overruling the Food and Drug Administration's decision to allow sale of morning-after pill without a prescription or regard for a person's age.
April 4, 2013 The Food and Drug Administration says it can't keep up with all the dietary supplements that claim to enhance sexual performance. Many have been found to contain potentially harmful ingredients, so the agency is warning people to beware of the entire bunch.
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