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In September 30, 2004, Merck officially announced of voluntary recall of Vioxx from all markets worldwide. A warning was issued to prevent people from taking
Vioxx and to return all unused pills. It also causes other life-threatening diseases, such as, blood clots, angina and nonbacterial meningitis, severe intestinal damage, ulcerations and bleeding, and kidney damage. Other minor side effects include flu symptoms, weakness, loss of appetite, rash or pail skin, swelling of hand feet and other extremities.
Many blamed
Food and Drug Administration or
FDA, because it is its duty to assure people of harmless foods and drugs. Also,
FDA was blamed for giving Merck a fast-track, 6-month approval process. Vioxx was distributed in
United States in 1999. They want FDA to push drug companies to conduct longer tests before they can sell it so that people are given
right warning.
In January 27, 2005,
consolidation of all Vioxx cases was argued in front of federal judges in Florida by
attorneys. A preliminary hearing will be held before
judge after
decision is made public. Now, there are web sites that offer free consultations for Vioxx victims.

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