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Discussion in 'Florida forum' started by rrhe6, Mar 4, 2018.

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    The study will use an Enriched Enrollment Randomized Withdrawal (EERW)
    design consisting of a 2-week open-label enrichment phase, during which
    subjects will receive etoricoxib. Patients who experience at least a 30% reduction
    in pain intensity will be randomized to either continued treatment with etoricoxib
    90 mg qd Etoricoxib at either dose led to significant improvement in other endpoints,
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    Etoricoxib given once daily provided significant relief of symptoms, and disability
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    was maximal Summary. Dysmenorrhoea is painful menstruation that occurs in 45–72% of all
    women. This was a prospective randomised study of the efficacy of etoricoxib (
    ArcoxiaВ®) compared with mefenamic acid (PonstanВ®) in treating primary
    dysmenorrhoea. All single, sexually inactive women with primary dysmenorrhoea
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    Analgesia: Acute Pain, Including that Related to Primary Dysmenorrhea and
    Minor Dental Procedures: Recommended Dose: 90 or 120 mg once daily.
    Arcoxia 120 mg should be used only for the acute symptomatic period; limited to
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    Arcoxia (etoricoxib) has been approved for the short-term treatment of moderate
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