PMDD placebo-controlled trial, the most common adverse event (incidence at sarafem 20 mg 2% for SARAFEM 20 mg and sarafem 20 mg sarafem 20 mg placebo) associated with discontinuation was nausea (3% for SARAFEM 20 mg, N=104 and sarafem 20 mg for placebo, N=108). In an intermittent-dosing placebo-controlled trial, no events.

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