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In both trials, the most common side effect was gastrointestinal symptoms, which affected about half of the patients on either dose and about a quarter of patients on the placebo

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In light of these revelations, in mid-2014 the US Food and Drug Administration (FDA) warned against the use of uterine power morcellation procedures (FDA 2014a), and some insurers stopped covering the cost of these operations (Reuters 2014b)

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