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Food and Drug Administration panel recommended that rimonabant should not be given the FDA's blessing because of continuing concerns about increased risks for suicidal thoughts among some users. Food and Drug Administration finding of increased risk of suicide during treatment with rimonabant, we recommend increased alertness by physicians to these potentially severe psychiatric adverse reactions. 25 percent increase in percent atheroma volume (PAV) in those taking rimonabant, compared to 0. Rimonabant is not yet accustomed for use in the United States, area it is accepted as Zimulti. Rimonabant is not yet approved for use in the United States, where it is known as Zimulti. 15 -- People who take the weight-loss drug rimonabant may face heightened risks for severe depression and anxiety, Danish researchers report.
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