teniposide (Vumon)
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Introduction
Tradename: Vumon.
Indications
- treatment of refractory childhood, acute lymphocytic leukemia (ALL) in combination with other antineoplastic agents
- non-Hodgkin's lymphoma
- neuroblastoma[3]
Dosage
Injection:
- formulated in polyethoxlated castor oil & dehydrated alcohol (43%): 10 mg/mL (5 mL)
Solution:
- solutions containing 0.5-2 mg/mL remain stable for 4 hours & those containing 0.1-0.2 mg/mL remain stable for 6 hours
Adverse effects
- common (> 10%)
- myelosuppression, leukopenia, neutropenia, thrombocytopenia, mucositis, nausea/vomiting, diarrhea, infection
- less common (1-10%)
- uncommon (< 1%)
- hepatic dysfunction, peripheral neurotoxicity, renal dysfunction, metabolic abnormalities
Drug interactions
- plasma clearance of methotrexate may be slightly increased
- salicylate, sulfamethoxazole & tolbutamide displace teniposide from protein binding sites to a small, but significant extent
Laboratory
test interactions: increases serum K+
Mechanism of action
More general terms
Additional terms
References
Database
- PubChem: http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=34698
- PubChem: http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=5396
- PubChem: http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=5311475
- PubChem: http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=5284623
- PubChem: http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=452548
- PubChem: http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=275784