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Vepesid Brand names, Vepesid Analogs

Vepesid Brand Names Mixture

  • No information avaliable

Vepesid Chemical_Formula

C29H32O13

Vepesid RX_link

http://www.rxlist.com/cgi/generic2/etopophos.htm

Vepesid fda sheet

http://www.accessdata.fda.gov/scripts/cder/onctools/labels.cfm?GN=etoposide,%20VP-16

Vepesid msds (material safety sheet)

Vepesid MSDS

Vepesid Synthesis Reference

No information avaliable

Vepesid Molecular Weight

588.557 g/mol

Vepesid Melting Point

236-251 oC

Vepesid H2O Solubility

58.7 mg/L

Vepesid State

Solid

Vepesid LogP

1.197

Vepesid Dosage Forms

Solution; Capsule; Liquid

Vepesid Indication

For use in combination with other chemotherapeutic agents in the treatment of refractory testicular tumors and as first line treatment in patients with small cell lung cancer. Also used to treat other malignancies such as lymphoma, non-lymphocytic leukemia, and glioblastoma multiforme.

Vepesid Pharmacology

Etoposide is an antineoplastic agent and an epipodophyllotoxin (a semisynthetic derivative of the podophyllotoxins). It inhibits DNA topoisomerase II, thereby inhibiting DNA synthesis. Etoposide is cell cycle dependent and phase specific, affecting mainly the S and G2 phases. Two different dose-dependent responses are seen. At high concentrations (10 µg/mL or more), lysis of cells entering mitosis is observed. At low concentrations (0.3 to 10 µg/mL), cells are inhibited from entering prophase. It does not interfere with microtubular assembly. The predominant macromolecular effect of etoposide appears to be the induction of DNA strand breaks by an interaction with DNA-topoisomerase II or the formation of free radicals.

Vepesid Absorption

Absorbed well, time to peak plasma concentration is 1-1.5 hrs. Mean bioavailability is 50%.

Vepesid side effects and Toxicity

Side effects include alopecia, constipation, diarrhea, nausea and vomiting and secondary malignancies (leukemia).

Vepesid Patient Information

Patients are generally advised to call their doctor in case of fever, symptoms of infection or painful injection sites, as these may progress severely without adequate medical attention. It is advised to drink lots of fluids after treatment to prevent damage to the bladder and kidneys, typically 1.5 to 3.5 litres of water on the day of treatment and for several days after.

Vepesid Organisms Affected

Humans and other mammals