Legal Headlines

July 31, 2007 12:00 AM

A FDA advisory panel on Monday found that people who use the popular diabetes pill Avandia face a greater risk of heart attack and urged the FDA to slap its strictest warning on its label.



July 30, 2007 12:00 AM

Diabetes drug Avandia should be removed from the market, public citizen tells FDA advisory committee popular drug associated with risks to multiple organ systems has no benefit over older, safer type 2 diabetes drugs.



July 30, 2007 12:00 AM

The widely used diabetes drug Avandia should be pulled from the market because of heart risks, a federal scientist said Monday.



July 29, 2007 12:00 AM

The U.S. FDA announced that it is permitting the restricted use of Zelnorm under a treatment investigational new drug protocol to treat irritable bowel syndrome with constipation and chronic idiopathic constipation in women younger than 55 who meet specific guidelines.



July 27, 2007 12:00 AM

For decades, Wyeth Pharmaceuticals marketed one of the nation's top selling drugs for relief. But now, there's a warning for women.



July 27, 2007 12:00 AM

The U.S. FDA announced that it is permitting the restricted use of Zelnorm (tegaserod maleate) under a treatment investigational new drug (IND) protocol to treat irritable bowel syndrome with constipation.



July 27, 2007 12:00 AM

The drug Zelnorm, manufactured by Novatis, was taken of the market in March because of a high risk of heart attacks, stroke, and chest pain.



July 27, 2007 12:00 AM

In 1974, then-judge Miles Lord issued an environmental ruling that reverberated through the Iron Range taconite industry. Thirty-three years later, he's still fighting to protect its workers  and the health of all Minnesotans.



July 27, 2007 12:00 AM

"My father started taking Avandia shortly after it was approved in 1999 but we didn't hear about the dangers of this drug until June of this year," says Pender.



July 27, 2007 12:00 AM

Arguments on two questions in federal Vioxx cases may wait on testimony from two governors who have worked in or for the drug industry about consultations with the FDA about drug label rules made last year.