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the most commonly observed adverse events associated with the use of paroxetine incidence of 5 or greater and incidence for paroxetine hydrochloride at least twice that of placebo, derived from table 3 were nausea, dry mouth, decreased appetite, constipation, dizziness, somnolence, tremor, sweating, impotence, and abnormal ejaculation.

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the potency of the ssris as inhibitors of the metabolism of the p450-p2-d6 varies and is reported in descending order of potency as paroxetine, fluoxetine, sertraline, citalopram, and fluvoxamine.

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the effectiveness of paroxetine hydrochloride in the treatment of panic disorder was demonstrated in three 10 to 12 week multicenter, placebo-controlled studies of adult outpatients studies 1 to 3 .

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hyponatremia may occur as a result of treatment with ssris and snris, including pexeva paroxetine mesylate .

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15 absolute risk; women using paroxetine during the first trimester of pregnancy were 28 more at risk of having a child with cardiac malformations 18 studies combined baseline risk of cardiac malformation is 1 and thus a 28 increased risk is 1.
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The use of mirtazapine, a noradrenergic and specific serotonergic antidepressant, versus paroxetine, a selective serotonin reuptake inhibitor, for the treatment of patients with depression in primary care.

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