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3.5% of 201 patients receiving 6.25 mg or 12.5 mg of Ambien CR discontinued treatment because of an adverse event in clinical trials with Ambien CR.
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The most generally observed adverse events associated with the use of Ambien CR were headache (19%), somnolence (15%), and dizziness (12%) during treatment with Ambien CR at daily doses of up to 12.5 mg for 3 weeks.