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Patients who had not previously received atorvastatin or who had not been receiving 10 mg of atorvastatin for at least 6 weeks before screening entered a 7-week run-in period, during which they received open-label therapy with 10 mg of atorvastatin.

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There was one serious adverse event of dehydration in a patient who received 80 mg of atorvastatin plus SAR236553; the event was not thought to be treatment-related.

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