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Drug: Etoposide
Brand: VP-16 20mg/mL
Manufacturer /
TM Owner
Generic
Origin: USA

VP-16 20mg/mL Injection

Formulated with Etoposide, VP-16 is a cytotoxic chemotherapy agent. It damages the DNA or division machinery of rapidly dividing cancer cells, halting tumour growth. It is used in the treatment of a range of cancers. It is supplied as an injection (20mg/mL). Treatment is individualised by the prescribing physician to balance efficacy and tolerability.
Strength: 20mg/mL
Pack Size: 1s
Storage: 20°C to 25°C
Form: Injection

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Indications & Clinical Uses

  • VP-16 20 mg/mL is an older abbreviation for etoposide and is not a current brand name found on DailyMed; the information below comes from the Etoposide Injection, USP 20 mg/mL labels (Fresenius Kabi USA and Meitheal).
  • Etoposide is a topoisomerase II inhibitor chemotherapy medicine.
  • In combination with other approved chemotherapy agents it is used for refractory testicular tumours and as first-line treatment of small cell lung cancer.
  • It is given only in hospital or clinic, by a healthcare provider experienced in cancer chemotherapy, as a slow intravenous infusion over 30 to 60 minutes after dilution to 0.2 to 0.4 mg/mL; it must not be given as a rapid injection.
  • Vials contain 100 mg/5 mL, 500 mg/25 mL or 1 g/50 mL.
  • Other etoposide products, such as oral capsules or etoposide phosphate, have different formulations and doses and must not be substituted for this injection.

Side Effects

  • BOXED WARNING: etoposide should be given under the supervision of a qualified physician experienced in cancer chemotherapy, and severe myelosuppression (bone marrow suppression) with resulting infection or bleeding may occur.
  • Low white blood cell counts affect 60 to 91 in 100 people (severe in 3 to 17), nausea and vomiting 31 to 43 in 100, and hair loss 8 to 66 in 100.
  • Anaphylactic-type reactions occur in 0.7% to 2% of patients receiving intravenous etoposide, and too-rapid infusion can cause low blood pressure.
  • Tell your care team at once about fever, chills, bleeding or bruising, breathing difficulty, wheezing, facial swelling or dizziness during or after the infusion.
  • Rarely, acute leukaemia has been reported after treatment.

Precautions & Warnings

  • Etoposide should be given only under the supervision of a physician experienced with cancer chemotherapy, in a setting able to manage severe myelosuppression and allergic reactions.
  • Blood counts are checked periodically; white cell counts typically fall lowest 7 to 14 days after a dose and platelets 9 to 16 days after.
  • It is contraindicated in people with hypersensitivity to etoposide or any ingredient; the injection contains benzyl alcohol, polysorbate 80, polyethylene glycol 300 and about 30.5% ethanol, which matters for sensitive patients.
  • Etoposide can cause fetal harm (Pregnancy Category D), so avoid becoming pregnant; it is not known whether it passes into breast milk, so a decision must be made whether to stop nursing or the drug.
  • Dose is reduced to 75% when creatinine clearance is 15 to 50 mL/min.
  • Hospital pharmacy stores vials at 20°C to 25°C, protected from light.

Avoid Interactions

  • Medicines that increase etoposide exposure or toxicity: high-dose cyclosporin A (concentrations above 2,000 ng/mL) increased etoposide exposure by 80% with oral etoposide and reduced its clearance; etoposide is metabolised through the CYP3A4 pathway, so medicines that affect CYP3A4 may change its levels; and other medicines that suppress the bone marrow may worsen low blood counts.
  • Medicines that reduce efficacy: none were listed in the label sections reviewed.
  • Etoposide must be diluted before use and must not be given by rapid intravenous injection.
  • Tell your healthcare team about all prescription medicines, herbal products and supplements, and about any planned vaccinations, before treatment.

References

Frequently Asked Questions

VP-16 is another name for etoposide injection, a chemotherapy medicine used with other cancer drugs to treat refractory testicular tumours and, as first-line treatment, small cell lung cancer. It is given only in hospital or clinic by a healthcare provider experienced in cancer chemotherapy.

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