Chantix Label Revision

February 27, 2008

FDA informed healthcare professionals and consumers of important revisions to the WARNINGS and PRECAUTIONS sections of the prescribing information for regarding serious experienced in patients taking . These symptoms include changes in behavior, agitation, depressed mood, , and attempted and completed . While some patients may have experienced these types of symptoms and events as a result of , some patients taking who experienced serious and events had not yet discontinued smoking. In most cases, developed during treatment, but in others, symptoms developed following withdrawal of therapy.

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More on Chantix

February 5, 2008

Many new drugs initially enjoy banner sales growth, only to get kneecapped by reports of previously unknown adverse side effects. On Friday, the FDA issued an alert “highlighting” a stricter warning label for one of ’s most important new drugs.

The compound in question, , is one of the most recent non-nicotine stop-smoking treatments on the market. The FDA approved it back in 2006, but after its launch, some of the more than 5 million patients who have tried the drug began to report adverse events, including anxiety, other serious , and “vivid” and “unusual” dreams. As a result of these reports, strengthened the warning label for . Last week’s FDA announcement formalized more specific for the drug’s label.

Learn More: Motley Fool

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FDA Says Stop-Smoking Drug May Pose Psychiatric Risks

February 2, 2008

The Food and Drug Administration issued a public health advisory about suicidal thinking and other psychiatric conditions in patients taking the smoking cessation drug , warning that it “may cause worsening of current psychiatric illness even if it is currently under control. It may also cause an old psychiatric illness to reoccur.”

Learn More: Washington Post

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