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Louisiana teachers' union concerned about educators' future; Supreme Court hears arguments in Trump immunity case; court issues restraining order against fracking waste-storage facility; landmark NE agreement takes a proactive approach to CO2 pipeline risks.

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Speaker Johnson accuses demonstrating students of getting support from Hamas. TikTok says it'll challenge the ban. And the Supreme Court dives into the gray area between abortion and pregnancy healthcare, and into former President Trump's broad immunity claims.

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The urban-rural death divide is widening for working-age Americans, many home internet connections established for rural students during COVID have been broken, and a new federal rule aims to put the "public" back in public lands.

Generic Drug Warning: The Warning Isn't Required

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Wednesday, August 29, 2012   

BALTIMORE - A U.S. Supreme Court decision a year ago makes it all but impossible to sue generic-drug manufacturers for failing to provide adequate warnings of a drug's dangers. A new proposal would change the law.

Across the nation, dozens of lawsuits against manufacturers of generic drugs have been dismissed because of the high court ruling - a decision Marylanders likely don't know about. The case, Pliva vs. Mensing, centered on whether generic manufacturers have to update warnings about drug dangers when safety issues surface with name-brand equivalents. The justices ruled that they're not required to do so.

Attorney Gary Leppla, who represented the family of a young woman who died after an adverse reaction to a generic medication, says generics aren't usually the patient's or doctor's choice.

"You have the drug manufacturers, insurance companies, really dictating medical practice. Doctors have the opportunity to be aware of the risks, and yet what is used to fill a prescription is not necessarily dictated by the doctor. It happens after it leaves the doctor's desk."

Insurance companies say generic drugs save money and have the same active ingredients as the brand names. Name-brand manufacturers are required by the federal Food and Drug Administration to constantly update their labels.

Proposed legislation would force makers of generics to update the warning label when a new safety issue arises. Leppla says it affects nearly everyone who gets a prescription filled.

"Why should I be treated different as a consumer because I was required to have my prescription filled with a generic, as opposed to the originally manufactured drug?"

Leppla says nearly 80 percent of all prescriptions in the United States are filled with generic drugs.

The proposed legislation is Senate Bill 2295 and House Resolution 4384.


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