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October 10, 2008

Litigation Into Perpetuity?

Drug Safety: A Lawyer’s View

A lawyer says litigation illuminates how the pharmaceutical industry thinks and conducts itself. A few forward-looking statements.

Trasylol, Bayer & Three Mile Island

Drug Safety Story Time

Reflections on the power of narrative and the industry’s wobbly reputation.

Three Ticking Clocks

Bayer Halts Trasylol Sales

With journal editors in charge of drug safety, the political system has failed the industry and the public. 

The Case For Outreach

Stopping Drug Safety Spin Cycle

Why the pharmaceutical industry’s ill-advised reliance on lobbyists will hamper its efforts to rehabilitate its reputation.

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Litigation Into Perpetuity?

Drug Safety: A Lawyer’s View

March 05, 2008

By Mark Uehling

When will the drug safety wars end? How will they end? A new president? A Supreme Court decision? We thought Tom Lamb might know. He’s an attorney based in Wilmington, North Carolina. Like it or not, lawyers like Lamb are…

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Trasylol, Bayer & Three Mile Island

Drug Safety Story Time

February 22, 2008

By Mark Uehling

With the Oscars upon us, it’s time to reflect on something simple. Our brains store information and make sense of the world in stories. This is true in all cultures, all individuals. “She saved my career.” “They worked it out.”…

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Three Ticking Clocks

Bayer Halts Trasylol Sales

November 07, 2007

By Mark Uehling

In another significant win for medical journal editors in their new role as regulators, Bayer suspended sales of anti-clotting drug Trasylol (aprotinin), which had been implicated in kidney failure, cardiovascular problems and mortality risk. The drug had approximately $135 million…

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The Case For Outreach

Stopping Drug Safety Spin Cycle

October 12, 2007

By Mark Uehling

A few years ago, thinking the way all journalists think, we had an epiphany. The reportorial brain is the one we’re happily stuck with. But it often adopts a harshly negative, critical outlook that transcends age, geography and political affiliation.…

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New Diabetes Endpoints?

NEJM Hits Post-Approval Trials

September 05, 2007

By Mark Uehling

Concerns about diabetes blockbuster Avandia have been addressed by the mass media, by FDA statements—and by the August 30, 2007, New England Journal of Medicine (NEJM). It’s not a surprise that the journal would have a negative view of the…

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Avandia, etrials, FDA on e-CRFs

News Briefs

May 22, 2007

By info@clinpage.com

GlaxoSmithKline took a bullet from the anti-industry New England Journal of Medicine, which did a meta-analysis of data about the GSK diabetes drug Avandia. The Cleveland Clinic’s Steve Nissen calculates Avandia to raise the odds of cardiovascular-related death by 64…