FDA Removes 500 Unapproved Prescription Drugs From The Market
The FDA has announced that it will be seeking to remove nearly 500 unapproved prescription drugs from the market. In a statement, the director of compliance at the Center for Drug Evaluation and Research notes that they "don't know what's in them, whether they work properly, or how they are made."
If believe you may have suffered a seriously or harmful side effect after taking a prescription drug, contact a New Mexico pharmaceutical malpractice lawyer for more information.
Often, a drug's potential for injury is unknown until patients begin reporting harmful side effects. It was only after years of studies and lawsuits that dangerous drugs such as Avandia and Vioxx received adequate warnings. Recent cases involving dangerous drugs such as Baycol, Bextra and Reglan have all brought to light the potential for debilitating side-effects and in some cases an increased chance of life-threatening effects from taking these harmful prescription drugs.
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