|  | | Interactions: |  | Cimetidine 
 Adverse Effect: An increased risk of fluorouracil toxicity
 
 Clinical Management: Monitor patients who have received long-term (four or more weeks) therapy with cimetidine for an increased incidence of adverse effects to fluorouracil. If possible, discontinue the cimetidine prior to the administration of fluorouracil. An alternative H-2 antagonist could also be substituted for cimetidine.
 
 Leucoverin
 
 Adverse Effect: fluorouracil toxicity (myelosuppression, stomatitis, GI toxicity)
 
 Clinical Management: Fluorouracil plus leucovorin is routinely used therapeutically in the treatment of cancer. Monitor patients, especially the elderly, for increased toxicity (myelosuppression, stomatitis, GI toxicity).
 
 Levamisole
 
 Adverse Effect: hepatotoxicity
 
 Clinical Management: Monitor patients for mild and asymptomatic hepatotoxicity, specifically, elevated alkaline phosphatase accompanied by increased transaminases or serum bilirubin. This hepatotoxicity is usually reversible.
 
 Metronidazole
 
 Adverse Effect: increased fluorouracil serum concentrations and fluorouracil toxicity (granulocytopenia, anemia, thrombocytopenia, stomatitis, vomiting)
 
 Clinical Management: Avoid concurrent administration of fluorouracil and metronidazole, if possible.
 
 Tamoxifen
 
 Adverse Effect: an increased risk of thromboembolism
 
 Clinical Management: In patients undergoing therapy with tamoxifen for breast cancer, the risks of adding fluorouracil should be weighed against the potential benefits.
 
 Warfarin
 
 Adverse Effect: an increased risk of bleeding
 
 Clinical Management:Adjustments of the warfarin dose may be necessary in order to maintain the desired level of anticoagulation.
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