floxuridine; fluorodeoxyurine; 2'-Deoxy-5-fluorouridine
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Indications
Dosage
- for intra-arterial infusion only
- 0.1 to 0.6 mg/kg/day
- doses of 0.4 to 0.6 mg for hepatic artery infusion
- reconstituted with 5 mL of sterile water for injection to yield a solution containing approximately 100 mg/mL of floxuridine
- the calculated daily dose(s) of the drug is then diluted with 5% dextrose or 0.9% sodium chloride injection to a volume appropriate for the infusion apparatus to be used
- therapy can be given until adverse reactions appear
Adverse effects
- procedural complications of regional arterial infusion (most common)[1]
- common:[1] nausea, vomiting, diarrhea, enteritis, stomatitis, localized erythema
- common laboratory abnormalities:
- anemia, leukopenia, thrombocytopenia
- elevations of serum alkaline phosphatase, serum AST, serum ALT, serum bilirubin & serum lactic dehydrogenase
More general terms
References
Database
- PubChem: http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=5790
- PubChem: http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=43834572
- PubChem: http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=643968
- PubChem: http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=46781591
- PubChem: http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=22824722