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Adverse Reactions Reported as Reasons for Discontinuation of Treatment in Adult Placebo-Controlled Trials Adverse Reactions Occurring at an Incidence of 5% or More Among Duloxetine Delayed-Release Capsules-Treated Patients in Adult Placebo-Controlled Trials Table 2 gives the incidence of treatment-emergent adverse reactions in placebo-controlled trials for approved indications that occurred in 5% or more of duloxetine hcl 60mg ec caps treated duloxetine hcl 60mg ec cap duloxetine delayed-release capsules and with an incidence greater than placebo.

a The inclusion of an event in the table is determined based on the percentages before rounding; however, the percentages displayed in the table are rounded to the nearest integer.1-92.

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In these studies, patients receiving duloxetine 60-120 mg daily had greater improvements in the Hamilton anxiety scale HAM-A total score and the Sheehan Disability Scale SDS global functional impairment score than did patients receiving placebo.The safety of doses above 120 mg once daily has not been evaluatedsee Clinical Studies.

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UTTING trusted. Since clinical experience in pediatric patients under 6 years of age is limited, the use of the drug in this age group mg, 2 to 4 times daily (may be increased in some pediatric The necessity of discontinuing therapy because of undesirable effects has been rare.


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