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Ohio Vioxx® Lawyers

VIOXX® SIDE EFFECTS

On September 30, 2004, Merck & Company, the manufacturer of Vioxx®, withdrew the drug from the market. Merck took this action after several studies clearly showed that people using Vioxx® for an extended period were at twice the risk for heart attack and stroke.

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The most recent study specifically revealed an increase in blood clots linked to heart attacks and strokes among people who used Vioxx® for at least 18 months as compared to those who took other arthritis drugs.

Prior to September 30, 2004, Merck refused to acknowledge that Vioxx® increased the risk for heart attacks and strokes, as well as other negative side effects. In fact, the FDA chastised Merck for minimizing Vioxx®'s risks to physicians and the public.

Merck had good reason to minimize these side effects. Vioxx® generated sales worth approximately $2.5 billion per year. Unfortunately, Merck's desire for higher profits put many Vioxx® patients at increased risk for heart attacks and strokes.

Clark, Perdue & List is a Columbus, Ohio law firm representing victims of Vioxx® side effects and their families throughout Ohio. Our Vioxx® side effects attorneys will make sure that Merck pays for the damages it inflicted on Vioxx® victims and their families.

Click here for more information about Vioxx®.

If you or someone you know has suffered serious side effects such as a heart attack or stroke from the use of Vioxx®, call or e-mail the experienced Ohio Vioxx® attorneys at Clark, Perdue & List today.

Read "The Vioxx® Disaster" by Andrew List from the Columbus Bar Briefs

Vioxx® Newsletter: February 2005

Vioxx® Newsletter: Summer 2005

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Cases We Handle

Bextra®

Fosamax®

Gadolinium®

Ketek®

Lamictal®

Ortho Evra®

Paxil®

ReNu®

Singulair®

Strattera®

Tequin®

Trasylol®

Vioxx®

Zevalin®

Contaminated Bone or Tissue Transplant

Guidant Defibrillator

Medtronic Defibrillator

Drug Eluting Stents (DES)

From Vioxx to Gadolinium,