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If fluoxetine or paroxetine is initiated in patients receiving IM risperidone 25 mg every 2 weeks, the manufacturer recommends continuing 25 mg every 2 weeks; dosage reduction to Adverse effects associated with discontinuance of therapy in at least 2 risperidone-treated patients were dizziness, nausea, vomiting, parkinsonism, somnolence, dystonia, agitation, abdominal pain, orthostatic hypotension, and akathisia.

Adverse effects associated with discontinuance of therapy in more than one risperidone-treated patient included dizziness, somnolence, sedation, lethargy, anxiety, balance disorder, hypotension, and palpitation.


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