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Trump’s Next Tariffs Target Could be Foreign-Made Pharmaceuticals

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Trump’s Next Tariffs Target Could be Foreign-Made Pharmaceuticals

Newer and more expensive medications are more likely to be made in the United States or Europe. Ireland, in particular, has become a hub because it is a tax haven.

Many of the industry’s biggest blockbusters are manufactured at least partly in Ireland. Among them are: Keytruda, Merck’s cancer drug; Zepbound, Eli Lilly’s weight-loss drug; and Stelara, Johnson & Johnson’s anti-inflammatory drug used for conditions like arthritis.

Mr. Trump has taken notice. “This beautiful island of five million people has got the entire U.S. pharmaceutical industry in its grasp,” he said in March at a meeting with Prime Minister Micheal Martin of Ireland.


U.S. production of pharmaceuticals peaked, by one measure, in 2006.

That was around the time a wave of top-selling American-made drugs lost patent protection, creating opportunities for generic manufacturers in India and China to ramp up production of generics. Around the same time, U.S. government incentives to manufacture in Puerto Rico were phased out, while new carrots, like tax advantages in Ireland, encouraged manufacturers to move production overseas.

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In 2021, most of America’s top-consumed generic drugs, as well as key antibiotics and antivirals, had no American facility producing their active ingredients, according to Clarivate.

Mr. Trump said on Wednesday that “the United States can no longer produce enough antibiotics to treat our sick.”

For example, nearly all the world’s sites producing the active ingredient of amoxicillin, a common antibiotic, are in China, India or Europe, according to Clarivate.

A Tennessee plant, now owned by a company called USAntibiotics, used to supply nearly all of the amoxicillin consumed in the United States. It now imports the active ingredient from Europe and uses it to formulate pills. The plant now supplies about 5 percent of America’s amoxicillin.

Medications are usually protected from tariffs under a World Trade Organization agreement aimed at protecting patients’ access to vital drugs. The tariffs that Mr. Trump imposed on certain imports in his first term did not hit pharmaceuticals.

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Starting in February, drugmakers importing active ingredients made in China into the United States have had to pay a tariff that Mr. Trump imposed on Chinese goods. That tariff rose to 20 percent in March. (Wednesday’s levies add a new 34 percent tariff on most Chinese imports, though that does not apply to medicines.)


For the manufacturers of inexpensive generic drugs with razor-thin profit margins, the added costs of tariffs could be “a tipping point” that prompts them to exit the market, said Erin Fox, an expert at the University of Utah who tracks drug shortages.

Dr. Fox said she was most worried about drugs for which shortages are already common, such as generic medications given as an injection. These injections are harder to make than pills and are much less profitable than newer medications, discouraging manufacturers from jumping in. An example is lidocaine, used to numb pain during medical procedures. Most production of lidocaine’s active ingredient is in India, according to Clarivate.

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The Next Wave of Weight Loss Science May Come From a Peptide Inside Your Body That Mimics Ozempic

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The Next Wave of Weight Loss Science May Come From a Peptide Inside Your Body That Mimics Ozempic


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The Natural Peptide in Your Body That Could Replace Ozempic




















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Americans to get new sunscreen option already used abroad for decades

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Americans to get new sunscreen option already used abroad for decades

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The Food and Drug Administration (FDA) is amending its list of permissible sunscreen ingredients for the first time in more than 25 years.

On Tuesday, the federal health agency signed off on allowing bemotrizinol to be added to sunscreen products after it met the FDA’s standard for protecting against dangerous ultraviolet rays and causing little irritation or absorption into the skin, according to the Associated Press.

This addition gives Americans access to a skin-protecting chemical that has been historically used in Europe and other parts of the world.

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Bemotrizinol will initially be sold in the U.S. as Parsol Shield, manufactured by Dutch company DSM Nutritional Products, expected to launch later in 2026, the AP reported. The ingredient will be available for use by other manufacturers after an 18-month exclusivity period.

The FDA has signed off on allowing bemotrizinol to be added to sunscreen products. (iStock)

DSM (the sunscreen ingredient company) submitted a format request for the FDA to approve bemotrizinol as a new sunscreen ingredient in the U.S., allowing its use in over-the-counter sunscreens at concentrations up to 6%.

In a December press release announcing the proposal of this request, the FDA noted that bemotrizinol is “generally recognized” as safe and effective for adults and children 6 months and older.

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FDA Commissioner Marty Makary, MD, MPH, commented in a statement that the agency has “historically moved too slowly in this area, leaving Americans with fewer options than consumers abroad.”

Bemotrizinol is “generally recognized” as safe and effective for adults and children 6 months and older, according to the FDA. (iStock)

“We’re continuing to modernize the regulation of sunscreen and other over-the-counter drug products,” he said in the release. “Americans deserve timely access to the best safe, effective and consumer-friendly over-the-counter products available.”

In the same news release, Karen Murry, MD, acting director of the Office of Nonprescription Drugs in Maryland, commented that bemotrizinol “would be a welcome addition to the current array of effective sunscreen active ingredients already available to American consumers.”

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“We look forward to working with other companies on bringing products containing other new active ingredients to market for a wide array of conditions in multiple therapeutic areas, in a much more timely fashion than was possible in the past,” she added.

The FDA encourages the public to use sunscreen with other protective measures. (iStock)

The FDA continues to regulate sunscreen products to ensure that they meet safety and effectiveness standards, while encouraging the public to use numerous protective measures.

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This includes using broad-spectrum sunscreens SPF 15 or higher to help reduce the risk of skin cancer and signs of aging, along with wearing protective clothing and limiting time in the sun.

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Why Women Over 50 Are Obsessed With Fiber-Rich Foods for Weight Loss

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Why Women Over 50 Are Obsessed With Fiber-Rich Foods for Weight Loss


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Fiber-Rich Foods for Weight Loss Help Women Over 50 Burn Fat Fast




















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