WASHINGTON — Federal regulators are investigating whether a group of arthritis drugs made by Abbott Laboratories, the Schering-Plough Corporation and other companies heighten the risk of cancer in youngsters.
The Food and Drug Administration said Wednesday that it had received 30 reports of children and young adults developing cancer while taking the drugs over the last 10 years.
The drugs include Abbott Labs’ Humira, Schering-Plough’s Remicade and Enbrel, which is marketed by Amgen and Wyeth. The drugs are prescribed to children with arthritis to block a chemical that causes inflammation. They are also used to treat children with the intestinal disorder Crohn’s disease.
The products, known as tumor necrosis factor blockers, are key revenue drivers for the companies. Abbott’s Humira was the company’s best-selling product last year with over $3 billion in sales. Remicade also topped Schering-Plough’s portfolio with sales of $1.65 billion.
http://www.nytimes.com/2008/06/05/business/05drug.html?_r=1&partner=MYWAY&ei=5065&oref=slogin