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VIOXX® SETTLEMENT ANNOUNCED
The law firms that comprise the Executive Committee of the Plaintiffs' Steering Committee of the federal multidistrict VIOXX litigation, as well as representatives of plaintiffs' counsel in state coordinated proceedings, have reached an agreement to resolve U.S. products liability VIOXX claims already filed against the company. Merck has set aside $4.85 billion to pay claims of U.S. plaintiffs who suffered myocardial infarctions or ischemic strokes.
The conditions in the agreement, which is open only to those cases filed or tolled on or before Nov. 8, 2007, include:
- To qualify, claimants will have to pass three gates: an injury gate requiring objective, medical proof of MI or ischemic stroke (as defined in the agreement), a duration gate based on documented receipt of at least 30 VIOXX pills, and a proximity gate requiring receipt of pills in sufficient number and proximity to the event to support a presumption of ingestion of VIOXX within 14 days before the claimed injury;
- Individual cases will be examined by administrators of the resolution process to determine qualification based on objective, documented facts provided by claimants, including records sufficient for a scientific evaluation of independent risk factors;
- The agreement provides that Merck does not admit causation or fault;
- Neither stroke claims that are hemorrhagic in nature nor transient ischemic attacks will qualify;
- Law firms on the federal and state Plaintiffs' Steering Committees and firms that have tried cases in the coordinated proceedings must recommend enrollment in the program to 100 percent of their clients who allege either MI or ischemic stroke;
- The parties agree to seek court orders from the four coordination judges requiring plaintiffs' attorneys to promptly register all of their VIOXX claims, whether filed or tolled, and to identify the alleged injury - in order to establish the universe of all existing claims in the United States;
- Participation conditions: payment obligations under the agreement will be triggered only if, by March 1, 2008 (subject to extension by Merck), plaintiffs enroll in the settlement process: (a) 85 percent or more of all currently pending and tolled MI claims, (b) 85 percent or more of all currently pending and tolled ischemic stroke claims; (c) 85 percent or more of all eligible claims involving a death; and (d) 85 percent or more of all eligible claims alleging more than 12 months of use; and
- This agreement applies only to U.S. legal residents and those who allege that their MI or ischemic stroke occurred in the United States.
Under the agreement, separate funds will be created by the Company in the amount of $4 billion for MI claims and $850 million for ischemic stroke claims. Once triggered, Merck's total payment for both funds of $4.85 billion is a fixed amount to be allocated among qualifying claimants based on their individual evaluation. While at this time the exact number of claimants covered by this agreement is unknown, the total dollar amount is fixed. Payments to individual qualifying claimants could begin as early as August 2008 and then will be paid over a period of time. Merck retains its right to terminate this process without any payment to any claimant, and to defend each claim individually at trial if any of the participation conditions in the agreement are not met.
Should you have any questions, please do not hesitate to contact Fred Thompson at (843) 216-9118 or fthompson@motleyrice.com or Carmen Scott at (843) 216-9160 or cscott@motleyrice.com. To view the official Merck press release, click here.
We will continue to keep you updated as more information becomes available.
If you or someone you know, has been injured by taking Vioxx, you may be entitled to compensation. If you would like to explore your legal rights, please provide the following information and it will be forwarded to a Motley Rice pharmaceutical attorney:
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Please contact us with any questions or if you'd like to explore your legal rights.
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