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US says Chinese heparin now safe

Workers sort pig intestines at a plant in China, the first step in producing the blood thinner heparin. Workers sort pig intestines at a plant in China, the first step in producing the blood thinner heparin. (Qilai Shen/Bloomberg News)
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Associated Press / May 13, 2008

SHANGHAI - A blood thinner manufactured in China and linked to dozens of deaths in the United States is now safe because of tighter testing and controls, a top American health official said yesterday, while warning that all US imports would face closer scrutiny.

The US Food and Drug Administration has linked 81 deaths and hundreds of allergic reactions to a contaminant found in Chinese-made shipments of the drug heparin.

"We have put in place processes that we believe can ensure the safety of the heparin supply within the United States," US Health and Human Services Secretary Mike Leavitt said.

He said all exporters of food, drugs, and other products must prepare to meet more stringent guidelines of quality and safety, following a raft of product safety problems stemming from lax standards among overseas producers, especially in China.

"We believe the system that we have for ensuring safety is a good one but completely inadequate for the future," Leavitt said.

"What you'll see from the United States is a substantial change in our strategy," he added, noting Washington's plans to station FDA inspectors in China and other foreign countries.

Leavitt said he was optimistic American and Chinese officials could soon resolve a dispute over the FDA's investigation into the cause of deaths and reactions linked to heparin.

Washington plans to set up FDA offices in China to help improve product safety following allegations that many of Beijing's exports - from toys to fish - are shoddy or dangerous.

China's drug safety agency has accused the United States of blocking its inquiry into the problem by refusing to provide details on victims and specifics about production. Beijing contends it is too early to conclude that a contaminant found in raw heparin exported to the United States caused the adverse reactions.

A report published Friday said the FDA was concerned that some medical facilities may still have heparin in stock.

Leavitt said the need to prevent a shortage of heparin, widely used in dialysis and other common medical procedures, required the FDA to find ways to maintain the supply and quality of the drug.

"The FDA is satisfied that that which is coming into the United States is safe," he said. "Testing regimens have been put in place to ensure that."

Leavitt was due to meet with China's minister of health to discuss various issues, including a viral outbreak that has killed at least 34 children and sickened thousands.

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