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Table 2 shows the incidence of treatment-emergent adverse events from combined Phase 3 placebo-controlled studies of LUNESTA at doses of 1 or 2 mg imovane in elderly adults (ages 65-86) .
Treatment duration in imovane these trials was 14 days .
The table includes only events that occurred in 2% or imovane more of patients treated with LUNESTA 1 mg or 2 mg in which the incidence in patients treated with LUNESTA was greater than the incidence in placebo-treated patients .
08 Table 2: Incidence (%) of Treatment-Emergent Adverse Events in Elderly Adults (Ages 65-86) in 2-Week Placebo-Controlled Trials with LUNESTA1 LUNESTA 1 mg LUNESTA 2 mg Accidental Injury Digestive System Skin and Appendages Unpleasant Taste Urogenital System Urinary Tract Infection Events for which the LUNESTA incidence was equal to or less than placebo are not listed imovane on the table, but included the following: abdominal pain, asthenia, nausea, rash, and somnolence . 21476 imovane FDA approved labeling text 1 .
Adverse events from Table 2 that suggest a dose-response relationship in elderly adults include pain, dry mouth, and unpleasant taste, with this relationship again clearest for unpleasant lunesta nih quetiapin stilnoct where to buy zopiclone cheap zopiklon snorta zimovane cheap tickets taste .
These figures cannot be used to imovane predict the incidence of adverse events in the course of usual medical practice because patient characteristics and other factors may differ from those that prevailed in the clinical trials .
Similarly, the cited frequencies cannot is lunesta going generic soon eszopiclona 2 mg uso do stilnoct work buy zopiclone sleeping tablets be compared with figures obtained from other clinical investigations involving different treatments, uses, and investigators .

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