| Subject: | Best Practices for Monitoring Prescribing Practices for Drugs with Black Box Warnings |
| Category: | Food and Drug Administration (FDA)
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| Published: | Mon, 26 Nov 2007 - 12:00 pm |
| The "black box" warning is the most serious warning placed on the labeling of a prescription medication by the FDA. Black box warnings are designed to highlight special problems, particularly those that are serious, and to give health care professionals a clear understanding of a potential medical complication associated with a drug. Black box warnings provide physicians with important insights as to how to prescribe a drug that may be associated with serious side effects in a way... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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