Scientist Who Cited Drug's Risks Is Barred From F.D.A. Panel

conjur

No Lifer
Jun 7, 2001
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http://www.nytimes.com/2004/11.../13fda.html?oref=login
The Food and Drug Administration has told a researcher that he cannot be part of an advisory panel that will meet early next year to review the safety of a class of drugs, COX-2 inhibitors, used to treat arthritis and pain. The reason, the agency said, is he publicly stated that he thought one of these drugs caused heart problems and that Pfizer, its maker, knew that and was covering it up.

The scientist, Dr. Curt D. Furberg, a professor of public health sciences at Wake Forest University School of Medicine in Winston-Salem, N.C., was not barred forever from the panel, an F.D.A. spokeswoman said. Instead, Dr. Furberg was asked not to participate when it took up an issue in which he was seen to have an intellectual conflict of interest.

"This is a routine procedure," said Victoria Kao, the spokeswoman. "They look at the members that will make up the committee, and they review them for each case to see whether they have a conflict of interest, financial or intellectual."

In September, Merck announced that it was withdrawing its COX-2 inhibitor, Vioxx, from the market after a clinical trial it was conducting showed an increased risk of heart attacks and strokes when patients took it for 18 months or longer. That raised questions about similar drugs made by Pfizer, Celebrex and Bextra, and the F.D.A. panel was charged with reviewing what is known about them.

The Vioxx findings were based on the strongest evidence - a clinical trial comparing the drug with a placebo. But no such evidence on heart attacks and strokes has been reported for Celebrex and Bextra.

There is, however, a scientifically weaker study, pooling data from 12 clinical trials, that Dr. Furberg and Dr. Garret A. FitzGerald, a cardiologist and pharmacologist at the University of Pennsylvania, completed recently. "Basically, we showed that Bextra is no different than Vioxx, and Pfizer is trying to suppress that information,'' Dr. Furberg told The New York Times this week.

Dr. Furberg said yesterday that he was surprised to be removed from the advisory committee.

"I had a call yesterday, out of the blue," from the F.D.A., "disinviting me," he said. The agency, he said, told him "the reason is that I have publicly expressed my views."

The F.D.A.'s decision is not unreasonable, said Dr. David Orentlicher, a physician, lawyer and ethicist at Indiana University. It is analogous to situations in which potential jurors with strong opinions about a case are excluded from juries, and judges with such opinions are recused from hearing cases. "It's a concern about open minds if you are asked to be a neutral, detached observer," he said.

There is a risk, however, Dr. Orentlicher said, and it is the same one that arises in death penalty trials, which exclude jurors who are strongly opposed to capital punishment.

"You have to be careful that you don't skew the panel," he said.

Dr. Furberg said he did not object to being removed from the panel, "if it's the same rule they apply to others." He still has the option of presenting his data, and his opinions, in a public comment period at the meeting. "I haven't decided yet, but several people have said, 'You should,' " Dr. Furberg said.
Not sure if it's routine or not but it's more like the m.o. of the Bush administration (heck, even like Reagan with his FDA appointments that allowed Aspartame to be approved in a matter of months of him taking office after the FDA had rejected it for 16 years prior.)
 

conjur

No Lifer
Jun 7, 2001
58,686
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In related news per Drudge:

URGENT: NYTIMES AND '60 MINUTES' PLAN SUNDAY SPLASHES ON DRUG COMPANY MERCK AND ITS HANDLING OF EVIDENCE THAT VIOXX MIGHT POSE HEART RISKS... NYT STORY 6,000+ WORDS, LEAD OF PAGE ONES /// CBS PLANS TO SHOW 'DOCUMENTS'... DEVELOPING...
 

Pliablemoose

Lifer
Oct 11, 1999
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Give me a freaking break, Merck pulled the drug before FDA required it, it was approved under the Clinton administration.

Vioxx is a prescription COX-2 selective, non-steroidal anti-inflammatory drug (NSAID) that was approved by FDA in May 1999

Now the mass tort lawyers will descend upon Merck & once again prove that tort reform is needed...
 

BBond

Diamond Member
Oct 3, 2004
8,363
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The Food and Drug Administration has told a researcher that he cannot be part of an advisory panel that will meet early next year to review the safety of a class of drugs, COX-2 inhibitors, used to treat arthritis and pain. The reason, the agency said, is he publicly stated that he thought one of these drugs caused heart problems and that Pfizer, its maker, knew that and was covering it up.

Absolutely ridiculous. And absolutely typical. :|

 

BBond

Diamond Member
Oct 3, 2004
8,363
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Originally posted by: Pliablemoose
Give me a freaking break, Merck pulled the drug before FDA required it, it was approved under the Clinton administration.

Vioxx is a prescription COX-2 selective, non-steroidal anti-inflammatory drug (NSAID) that was approved by FDA in May 1999

Now the mass tort lawyers will descend upon Merck & once again prove that tort reform is needed...

A major pharmaceutical house peddles a drug they KNOW is harmful and you complain about tort reform?

What are all the people who used Vioxx for years supposed to do? Just roll over and die? Because that's what many of them are doing and all because of the willful negligence of Merck.

Funny how people attack lawyers when they're protecting people's rights, yet these same people are the first to call their lawyers when they need to head up to the Supreme Court.

 

Pliablemoose

Lifer
Oct 11, 1999
25,195
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Originally posted by: BBond
Originally posted by: Pliablemoose
Give me a freaking break, Merck pulled the drug before FDA required it, it was approved under the Clinton administration.

Vioxx is a prescription COX-2 selective, non-steroidal anti-inflammatory drug (NSAID) that was approved by FDA in May 1999

Now the mass tort lawyers will descend upon Merck & once again prove that tort reform is needed...

A major pharmaceutical house peddles a drug they KNOW is harmful and you complain about tort reform?

What are all the people who used Vioxx for years supposed to do? Just roll over and die? Because that's what many of them are doing and all because of the willful negligence of Merck.

Funny how people attack lawyers when they're protecting people's rights, yet these same people are the first to call their lawyers when they need to head up to the Supreme Court.

I :heart: lawyers, I do not like mass tort laywers, the consumer gets screwed by everyone in mass torts. I'm currently the lead palntiff in a mass tort case. I also have nearly 1/2 dozen lawyers employed at any given time.

As far as Merck, if they knew the drug hurt people sooner than they admitted, they need to go down & I'm all for criminalizing this kind of activity.

Our FDA is one of the best of this type in the world.
 

Hayabusa Rider

Admin Emeritus & Elite Member
Jan 26, 2000
50,879
4,267
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This is OK guys. Normal proceedure. Just like a judge recusing himself. Heaven knows I'll rake Bush over the coals, but it's just like it says to ensure freedom from bias.