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Podofilox Topical Solution

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Podofilox Topical Solution

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OVERDOSE

Topically applied podofilox (podofilox) may be absorbed systemically (see CLINICAL PHARMACOLOGY section). Toxicity reported following systemic administration of podofilox (podofilox) in investigational use for cancer treatment included: nausea, vomiting, fever, diarrhea, bone marrow depression, and oral ulcers. Following 5 to 10 daily intravenous doses of 0.5 to 1mg/kg/day, significant hematological toxicity occurred but was reversible. Other toxicities occurred at lower doses. Toxicity reported following systemic administration of podophyllum resin included: nausea, vomiting, fever, diarrhea, peripheral neuropathy, altered mental status, lethargy, coma, tachypnea, respiratory failure, leukocy-tosis, pancytosis, hematuria, renal failure, and seizures. Treatment of topical overdosage should include washing the skin free of any remaining drug and symptomatic and supportive therapy.

CONTRAINDICATIONS

Podofilox (podofilox) Topical Solution 0.5% is contraindicated for patients who develop hypersensitivity or intolerance to any component of the formulation.

Last reviewed on RxList: 6/14/2005
This monograph has been modified to include the generic and brand name in many instances.

Podofilox Topical Solution - User Reviews

Podofilox Topical Solution User Reviews

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