Judge Reverses $27M Verdict In Hormone Case

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hormonereplacementtherapyThe federal judge presiding over the Prempro federal litigation yesterday reversed a jury’s $27 million punitive damages award last March to a woman who claimed she developed breast cancer after using hormone replacement drugs, according to Mealy’s Litigation Report.

US Judge William Wilson of the Eastern District of Arkansas ruled that expert testimony provided by the plaintiff’s expert was improperly admitted and he ordered a new trial. And he apologized to the jury by saying the reversal was his own fault. “I admitted much evidence that should not have been admitted,” he wrote at the conclusion of his 52-page ruling.

On March 6, the jury ordered Wyeth to pay $19.4 million and Pfizer’s Pharmacia unit to pay $7.7 million after finding that the drugmakers acted inappropriately in marketing their hormone replacement therapies - Prempro, Premarin and Provera. But a May 9 hearing was held after the drugmakers filed motions seeking to toss the damages or obtain a new trial.

However, Wilson decided that portions of the testimony given by Suzanne Parisian, a regulatory expert for plaintiff Donna Scroggin, regarding certain company and FDA documents shouldn’t have been admitted during the punitive damages phase because they were outside the parameters of her expert report or the scope of her qualifications. Here is the ruling and Wyeth’s statement.

“Dr. Parisian was designated to testify on regulations and the standards and practice in the industry based on her experience,” Judge Wilson wrote on page 19. “Yet, Dr. Parisian’s punitive damages stage testimony was hardly expert in nature. The question and answer sessions merely paid lip service to Dr. Parisian testifying from an expert standpoint.”

As a result, Wilson ruled that Scroggin failed to present sufficient evidence to warrant punitive damages. “Since this case lacked substantial evidence, I should not have submitted the punitive damages issues to go to the jury,” he wrote on page 49. “Plaintiff presented evidence of what, at first blush, might be considered unsavory practices (e.g. ghostwriting, advertising, countering negative press, etc.), but it falls short of establishing a submissible jury issue.”

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  1. I was on the jury that awarded the damages to the plaintiff and I just wanted to say that I hope that the drug companies wake up and realize that they are responsible for may lives and should tell the whole truth about their drugs and do the necessary test to ensure that the drugs they put out are safe. What I got out of the time we listened to the testimony was that the drug companies knew that testing wasn’t done on the effects of the two drugs used together when the doctors were using them for many years together, they have the money to do test trials but didn’t.

  2. My mother took both as well. She had an early menopause as well. She had hot flashes and all of those symptoms as well. She got a cancer that is very much attributed to genetics. There is no history of pancreatic cancer in her family whatsoever. She died in 1998. It’s been just released that the two products she was taking for about ten years or so are carcinogens.

    Is there an attorney out there?

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