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Vioxx
drug liability - a new mass tort
Medical & Legal Perspectives
By Guerry R. Thornton, Jr. (Contact information about the author at the end of the article)
Copyright © - Guerry R. Thornton, Jr. 2004
Continued from Vioxx
drug liability: Background on a new mass tort
THE LEGAL RESPONSE
The chain of responsibility begins with Merck, and it can ultimately lead to pharmacies and health care providers. As health concerns first surfaced in 2001 and the FDA required cardiovascular warnings in 2002, an injured party can pursue many options. First, class actions can seek medical monitoring and refunds, but cannot provide fair awards for pain and disability. Thus, victims usually rely on direct suits to achieve the optimum results, which may include the specter of punitive damages under allegations that Merck had advance knowledge of heart dangers and failed to warn Vioxx users.
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A large number of suits can result in supervision by the Panel on Multi-District Litigation under 28
U.S.C. Sec. 1407 for the purpose of transferring federal cases to one venue to coordinate discovery and to achieve consistency of rulings and judicial economy. See, In Re Diet Drug Litigation, MDL No. 1203 (ED PA). The MDL judge will exercise enormous control over proceedings. In the implant case, the large number of claims justified MDL status. See, Breast Implant Litigation, MDL 926
(USDC AL). The transfer resulted in a "global settlement" with complex rules, a claims process and control over future suits. Judges can also become "gatekeepers", and can screen testimony to make certain experts are "reliable" and "qualified".
The diet drug and implant experiences show how Vioxx claims might play out in the courts. Each case involved thousands of claimants with injuries ranging from minor to severe. Lower level victims can often benefit from a common resolution plan, but the seriously injured can be held hostage by restrictive rules that may not provide a fair remedy. Although the right to a jury trial is protected, serious claims may have to wait years and must comply with complex pre-trial options before they get their day in court. Because federal oversight limits how individual cases proceed, many
Vioxx victims may choose to file in state court and proceed against pharmacies or health care providers. Claims relate to failure to warn, negligence, strict liability, and disregard for consumer safety. See, Wells v. Ortho Pharmaceutical Corp., 615 F.Supp. 262 (ND GA 1985).
Once a claim is discovered, it must be brought within a certain period of time after injuries are manifest (two years in Georgia). In a claim against a doctor, the bar date may run from the date of negligent therapy. See, O.C.G.A. Sec. 9-3-71. The decision to file requires a full legal-medical review. If a victim is a class member, an action will only involve filing a claim form.
Vioxx claims in federal court will probably be supervised by an MDL judge. In serious cases, a plaintiff may want to keep the case in state court for the best result, with the right to utilize rulings from the federal system. In many mass tort cases, awards in state jury trials have been much larger than values in MDL settlement plans.
Merck will be expected to take an aggressive stance and focus on alternative medical causes related to heart disease. Because heart disease involves genetic and life-style factors, Merck will challenge the proximate cause between Vioxx and cardiovascular events alleged in a claimant's suit. The company may also attempt to limit mass filings by fighting minor or problematic cases and paying fair compensation in viable, serious claims to avoid highly publicized jury awards and punitive damages.
One critical factor which will determine the size of the Vioxx litigation and the ultimate exposure of Merck will be the number of existing claims and the extent of future liability. Because the drug may clear out of the system after 10 days of usage, serious claims (heart attacks, death, ischemic strokes) may be identifiable in the first stage of litigation. Also, plaintiff's lawyers may focus on catastrophic injuries and not bundle serious claims with minor ones. In other drug cases, such as Baycol, the defense made it difficult to prosecute mid-level injury claims because of the cost of litigation versus succeeding at trial. The cost-benefit analysis may limit the total number of Vioxx cases with the majority of claims being pursued falling in serious injury categories. If this transpires, the litigation may be more manageable than prior mass tort cases, such as Fen-Phen. |
CONCLUSION
Vioxx victims will face challenges and great opportunities as the court system responds. A victim is usually faced with one suit based on death or irreparable injury. Now, the judiciary handles thousands of mass tort claims, and courts can fashion resolution options, ranging from medical benefits and health monitoring to matrix value settlements and jury trials. The seriously injured should be afforded special rights, including the expediting of claims and a full jury trial.
As the Vioxx saga plays out in the courts, the lessons of Dalkon Shield and its progeny should be improved so that those with serious claims are given priority and not treated equally with low-level and mid-level injury claims. As the dust settles from Merck's recall, courts will render decisions that protect the rights of all litigants.
About the author
Guerry R. Thornton, Jr. is a lawyer in Atlanta and a member of the State Bar of Georgia; he has prosecuted claims in the $2.5 billion Dalkon Shield Plan and the $4.5 billion Fen-Phen settlement; he has published articles on mass tort litigation in Trial and The National Law Journal; his internet site is: www.netlaw.net. He may be reached at tele-404/467-1670 or by email grthorntonjr@att.net
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