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Safety questions arise on blood clot drug
Seattle Post-Intelligencer ^ | January 17, 2006 | CARLA K. JOHNSON

Posted on 01/18/2006 12:16:47 AM PST by neverdem

ASSOCIATED PRESS

CHICAGO -- A hemophilia drug has been linked to deaths, strokes, heart attacks and other complications in patients given the medicine for other types of out-of-control bleeding, such as cerebral hemorrhages, according to FDA researchers.

The medicine, NovoSeven, is a clotting drug that was introduced in 1999 after being approved by the Food and Drug Administration to stop bleeding in hemophiliacs. But it has also shown promise in treating cerebral hemorrhages, a potentially lethal type of stroke involving bleeding in the brain.

Most of the reported complications followed off-label use - that is, uses for which the drug was not specifically approved by the FDA. Off-label use is legal, but doctors have less information on possible side effects of such uses.

The report on the complications appears in Wednesday's Journal of the American Medical Association.

The authors, including Dr. Kathryn O'Connell of the FDA's Center for Biologics Evaluation and Research, called for rigorous safety studies of new uses for the drug, which is made by the Danish pharmaceutical company Novo Nordisk.

NovoSeven got fast-track approval as an orphan drug, which means the company received financial incentives to develop it because it treats a rare condition and was seen as having little potential for profit.

Novo Nordisk AS said in a statement that off-label use of NovoSeven has resulted in complications in older people and those with underlying heart disease and acute injuries. The risk for approved uses "is thought to be low," the company said.

The company changed the warning in the package insert in October to include information on side effects in patients without hemophilia. Novo Nordisk said it is conducting studies on the safety of NovoSeven in such patients.

The researchers analyzed 431 reports to the FDA of adverse events, ranging from nausea to death, during the first five years of the drug's use. Drug makers are required to report such side effects when they happen during research on the drug after its approval. Doctors report them voluntarily.

In 185 cases, the drug's clotting action may have led to problems such as strokes and heart attacks, according to the study. Most of those problems followed off-label uses and happened within 24 hours of the last dose.

When it was introduced, NovoSeven was thought to be helpful for only the 10 percent of hemophilia patients who do not respond to standard treatments. The genetically engineered drug cost about $7,500 per dose.

Doctors have since found more uses for NovoSeven, including stemming bleeding from surgery, injuries or strokes. Use increased from 349 patients in 2000 to more than 4,500 in 2004.

"You're seeing people grasping for what's on the shelf now, hoping the evidence will follow," said Dr. James Meschia, a neurologist at the Mayo Clinic in Jacksonville, Fla.

Meschia's clinic has used the drug in life-threatening emergencies to try to stop bleeding in patients taking the anti-clotting drug warfarin. Since 2002, the clinic has used the drug off-label for seven patients and it caused no clotting difficulties, Meschia said.

In an October financial statement, Novo Nordisk reported global sales of NovoSeven increased 15 percent to $598 million for the first nine months of the year over the same period the previous year.

Last year, a study funded by the manufacturer and published in the New England Journal of Medicine showed NovoSeven can help patients with bleeding strokes. That study also turned up some complications, including heart attacks and strokes caused by blood clots.

Novo Nordisk shares fell 46 cents to close at $55.70 Tuesday on the New York Stock Exchange.

On the Net:

JAMA: http://jama.ama-assn.org


TOPICS: Business/Economy; Culture/Society; Extended News; Government; News/Current Events; US: District of Columbia; US: Maryland
KEYWORDS: novoseven
JAMA abstract Thromboembolic Adverse Events After Use of Recombinant Human Coagulation Factor VIIa
1 posted on 01/18/2006 12:16:48 AM PST by neverdem
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To: neverdem
Sorry, this seems like a duh! Naturally a drug that increases the ability to clot, albeit temporarily would directly increase the risk of thrombosis events. The clotting pathways and clotting factors/ proteins are very complex and it is difficult to regulate the body's response to outside manipulation via drugs, thus the need to regularly monitor patients on coumadin.
2 posted on 01/18/2006 2:45:00 AM PST by momincombatboots (Those who are too smart to engage in politics are punished by being governed by those who are dumber)
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To: momincombatboots
Sorry, this seems like a duh!

Yeah, it's like firearms discharge lethal projectiles, but the FDA is paying attention.

3 posted on 01/18/2006 2:52:49 AM PST by neverdem (May you be in heaven a half hour before the devil knows that you're dead.)
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To: neverdem

Thanks for the post and the info!


4 posted on 01/18/2006 5:24:06 AM PST by BlueAngel
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To: El Gato; JudyB1938; Ernest_at_the_Beach; Robert A. Cook, PE; lepton; LadyDoc; jb6; tiamat; PGalt; ..
W.Va. scientists discover superbubble

Iraq tests for bird flu after girl dies in north (Turkey - 8+ cases yesterday - one confirmed)

FReepmail me if you want on or off my health and science ping list.

5 posted on 01/18/2006 9:09:09 AM PST by neverdem (May you be in heaven a half hour before the devil knows that you're dead.)
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