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On average, patients lost more than 10 percent of their total body mass.But at Qnexa’s first FDA panel in 2010, experts assembled by the food and drug regulator voted 10 6 to not recommend the drug’s approval. Panelists said the drug was associated with a number of dangerous side effects, including suicidal thoughts, heart palpitations, memory lapses and birth defects.On Wednesday Vivus will offer to conduct a follow up study to monitor patients for any heart problems, if Qnexa is approved. Experts will consider whether the company should be required to conduct that study before FDA gives approval.