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The drug is well absorbed in the GI tract, but has extensive first pass metabolism which limits the amount of drug that enters the systemic circulation. It is metabolized primarily in the liver, distributes well into fatty tissue, and is excreted in breast milk, urine and feces.
*Note: the half life of the drug may increase after multiple dosings.
Do not use together with MAO inhibitors, may cause seizures, and death.
Avoid giving with cimetidine, may enhance antidepressant effect.
Avoid use with St. John’s wort, SAM-e, and yohimb.
Use cautiously in rats with a history of seizure activity as seizure threshold may be lowered.
CV: disturbances in heart rhythm.
CNS: lethargy, nervousness, seizures.
GI: changes in appetite, reduced intestinal motility, hard stools, or diarrhea.
GU: difficulty urinating or having urine retention or increased potential for urinary tract infection.
Skin: pruritus (itching ), skin dryness.
Posted on February 20, 2005, 16:25,
Last updated on December 15, 2008, 13:41
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