
LONDON, Oct. 24 (UPI) -- The European Medicines Agency is calling for suspension of marketing for the anti-obesity drug Acomplia after reports of psychiatric risks.
The EMEA's Committee for Medicinal Products for Human Use concluded that the benefits of Acomplia no longer outweigh its risks, the agency said Thursday. The drug rimonabant, marketed by Sanofi-Aventis as Acomplia, was approved for sale in the European United in 2006.
The agency said recent studies suggest an approximate doubling of the risk of psychiatric disorders in obese or overweight patients taking Acomplia compared to those taking placebo.
"Prescribers should not issue any prescriptions for Acomplia and should review the treatment of patients currently taking the medicine," the EMEA said in a statement. "Patients who are currently taking Acomplia should consult their doctor or pharmacist at a convenient time to discuss their treatment. There is no need for patients to stop treatment with Acomplia immediately, but patients who wish to stop can do so at any time."
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