First N.J. Vioxx Trial Involving Long-term Use Draws To An End

Will Jury Verdict Be For Plaintiffs Cona And McDarby, or Defendant Merck?

The first two Vioxx cases in New Jersey involving long-term Vioxx use, Cona v. Merck and McDarby v. Merck, may have a jury verdict as early as the first week of April 2006. 

Closing arguments are scheduled to take place in an Atlantic County, NJ courtroom on April 3, 2006, when lawyers for the two plaintiffs and the drug company will talk one last time to the jury about the factual evidence presented during the month-long trial.  Thereafter, Superior Court Judge Carol Higbee will provide the jury instructions that establish the legal standards to be used by the jurors (six women and two men) as they deliberate the issue of whether Merck should be held liable for the heart attacks suffered by Mr. Cona and Mr. McDarby while using Vioxx.

Dr. Margaret Harbison, a psychiatrist who treated plaintiff Thomas Cona for about four years beginning in August 2000, was the final witness put on by Merck’s lawyers. Dr. Harbison’s testimony was intended to counter earlier testimony from Mr. Cona’s daughter that her father was weak and unable to participate in family activities after his June 2003 heart attack. In summary, Dr. Harbison testified that Mr. Cona never mentioned taking Vioxx, neither before nor after his heart attack, and that just three months after his heart attack Mr. Cona said he was "feeling good" and playing golf again.

Under cross-examination by Mr. Cona’s lawyer, however, Dr. Harbison admitted that the doctors who were treating Mr. Cona for his heart attack — which doctors were not called to testify as part of Mercks’ defense case — would likely have better information about Mr. Cona’s Vioxx use, and his physical condition following the heart attack in 2003.

Here is a quick re-cap of this Vioxx trial prior to Dr. Harbison’s being called as the final witness:

  • Lawyers for plaintiffs Thomas Cona and John McDarby called 14 witnesses to present their respective cases.
  • Merck’s lawyers called only five witnesses: two company scientists; two cardiologists; and, as mentioned above, Mr. Cona’s psychiatrist.
  • The essence of the two plaintiffs’ cases was that Merck knew Vioxx caused an increased risk of heart attacks long before it recalled Vioxx, but did not warn doctors and patients because the drug company wrongfully placed profits over safety.
  • The theme of Merck’s defense was that the drug company acted responsibly as regards Vioxx, and that it was the men’s pre-existing medical conditions, not Merck’s Vioxx, that were to blame for their heart attacks.

A March 30, 2006 article by Reuters succinctly captured the positions of both sides as these two Vioxx cases go to the jury in New Jersey next week:

" ‘I think the evidence has showed that Merck acted responsibly in testing the medication before it was approved for market and continued to test the medicine after approval and that all the information was shared with the FDA,’ Merck spokesman Chuck Harrell said outside the courtroom."

"Asked for a comment as the trial drew to a close, [Mr. Cona’s lawyer, Mark Lanier] said, ‘I’d rather be sitting in my chair than Merck’s.’ "

Vioxx was pulled off the market in September 2004.  To date, more than 9,650 lawsuits concerning Vioxx have been filed against Merck in the U.S.  The consensus seems to be that the two verdicts in this first New Jersey trial involving long-term Vioxx use will have a significant impact on the Vioxx litigation overall, going forward.

(Posted by: Tom Lamb)

3 responses to “First N.J. Vioxx Trial Involving Long-term Use Draws To An End”

  1. Tom Lamb Avatar

    Two observations about the split verdicts in this NJ Vioxx trial.
    First, “samples” cases are going to be difficult cases for the plaintiff to win. Merck apparently persuaded jurors that Mr. Cona (whom the jury awarded nothing for his heart attack) did not take Vioxx for 22 months, as he claimed. Merck did so by pointing out that Mr. Cona had only filled three Vioxx prescriptions, which gave him a drug supply sufficient for seven months of daily use, only. Mr. Cona contended he had received enough free Vioxx samples from doctors to cover the other 15 months of alleged Vioxx use.
    Second, cases for plaintiffs with pre-existing cardiovascular risks are seemingly okay — and perhaps even better than cases involving people who were healthy before their heart attack. Mr. McDarby (whom the jury awarded $3 million for his heart attack, and another $1.5 million to his wife) had these heart-attack risk factors: age (77), gender, diabetes, and atherosclerosis.
    Thanks for reading Drug Injury Watch.
    Tom Lamb

  2. Hank Greenspan Avatar

    The “willful and wanton” verdict and withholding info from the FDA opens Merck to potential criminal prosecution via the Dept. of Justice (for committing fraud against the FDA). As far as I’ve determined, however, the FDA’s Office of Special Investigations has never, since its founding in ’92, prosecuted a case for fraud during the NDA or post-approval process. Does anyone have examples othewise?? (This would exclude off-label prosecutions (a la Neurontin), manufacturing defects, devices (a la Guidants), etc. I have found two earlier cases–Oraflex and Selacryn–but these were before the FDA’s Office of Criminal Investigations established. Both resulted in misdemeanor wrist-slaps.
    Thanks.

  3. Tom Lamb Avatar

    According to an April 13, 2006 article in the Newark (NJ) Star-Ledger newspaper, a spokesman for New Jeresy Attorney General Zulima Farber said they are leaving the matter of a state criminal investigation in the judiciary’s hands. A jury ordered Merck to pay $9 million in punitive damages, which means they can also refer the case for an investigation of a possible “criminal act.” This law was passed 11 years ago as part of a tort reform act.
    Here’s a link to the article:
    http://www.nj.com/search/index.ssf?/base/business-0/114490579643940.xml?starledger?bpha&coll=1
    Thanks for reading Drug Injury Watch.
    Tom Lamb

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