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Pharmaceutical Litigation

Vioxx®

Manufacturer: Rx Merck Research Laboratories
Uses: Cox-2 inhibitor designed to relieve the signs and symptoms of osteoarthritis and rheumatoid arthritis in adults.

If you have taken or are taking Vioxx,
please contact us immediately.


More Information

Prozac
Vioxx

ALERT! Update as of September 30th, 2004 from MedWatch - The FDA Safety Information and Adverse Event Reporting Program Vioxx Vioxx

Merck & Co., Inc. announced a voluntary withdrawal of Vioxx (rofecoxib) from the U.S. and worldwide market due to safety concerns of an increased risk of cardiovascular events (including heart attack and stroke) in patients on Vioxx. Vioxx is a prescription COX-2 selective, non-steroidal anti-inflammatory drug (NSAID) that was approved by FDA in May 1999 for the relief of the signs and symptoms of osteoarthritis, for the management of acute pain in adults, and for the treatment of menstrual symptoms, and was later approved for the relief of the signs and symptoms of rheumatoid arthritis in adults and children.

Read the 2004 MedWatch safety summary, including links to the Public Health Advisory, press release, and Q&As, at:

 http://www.fda.gov/medwatch/SAFETY/2004/safety04.htm#vioxx

Vioxx (Rofecoxib) and Celebrex are drugs that are prescribed by physicians to relieve pain, including pain from arthritis, pain from menstrual cycles, and other general sources of acute pain.

Recently, an advisory panel of the Food and Drug Administration recommended to the FDA that Vioxx's label should warn physicians and patients of a possible increased risk of heart attacks or other adverse cardiovascular events. In addition, an article recently appeared in the Journal of the American Medical Association that raises "a cautionary flag" about the risk of heart attacks or other adverse cardiovascular events associated with the usage of COX-2 inhibitors such as Vioxx and Celebrex. COX-2 inhibitors such as Vioxx and Celebrex have been shown to increase blood pressure in patients, which in turn can increase a patient's risk of stroke, heart attack, and/or other adverse cardiovascular events. In addition, the makers of Vioxx and Celebrex have received several reports of possibly kidney dysfunction and/or kidney failure associated with the usage of these drugs. Contact Us About Your Legal Rights #

Contact us by telephone at 1-800-305-7552. There is no charge to you for the telephone consultation.

We work on a contingent fee basis. We only get paid if you recover compensation.


Side Effects

  • Increased risk of heart attack
  • Increased risk of stroke
  • Increased blood pressure

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Recall News
DIGITEK RECALL!

The FDA has recalled all Digitek tablets after the discovery of manufacturing defects.  Individuals taking Digitek tablets may suffer from an illness known as Digitalis Toxicity and various other symptoms.  This manufacturing defect may cause serious health problems, and even death.   

Product Recall
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