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In these patients, during titration, the individual doses should be reduced. If higher doses are required, individual doses should be increased rather than dosing frequency. These patients should be monitored closely for the onset or increase in severity of the common adverse events dry mouth, somnolence, asthenia and dizziness as potential indicators of excessive overdose.

   
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If you have any of these conditions, you may not be able to use this medication, or you may need a dose adjustment or special tests during treatment. FDA pregnancy category B.

   
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