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With this regimen in those studies, the following adverse events were reported for paroxetine hydrochloride controlled-release tablets, at an incidence of 2 or greater for paroxetine hydrochloride controlled-release tablets and were at least twice that reported for placebo dizziness, nausea, nervousness, and additional symptoms described by the investigator as associated with tapering or discontinuing paroxetine hydrochloride controlled-release tablets e.

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Nevertheless, the physician who elects to use paroxetine tablets, usp for extended periods should periodically re-evaluate the long-term usefulness of the drug for the individual patient.

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There are no clinical studies of the combined use of ect and paroxetine tablets.

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Events reported upon discontinuation of treatment with paroxetine in the pediatric clinical trials that included a taper phase regimen, which occurred in at least 2 of patients who received paroxetine and which occurred at a rate at least twice that of placebo, were emotional lability including suicidal ideation, suicide attempt, mood changes, and tearfulness , nervousness, dizziness, nausea, and abdominal pain see discontinuation of treatment with paroxetine .

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Paroxetine has demonstrated efficacy for the treatment of social anxiety disorder in adults and children.

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short half life and the lowest dose of paroxetine that comes in a tablet equals there is no slow tapering method available unless you choose to switch to the liquid form.