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Drug: Etoposide
Brand: Vepesid 50mg
Manufacturer /
TM Owner
Amneal Pharmaceuticals NY LLC
Origin: USA

Vepesid 50mg Capsule

Formulated with Etoposide, Vepesid 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 a capsule (50mg). Treatment is individualised by the prescribing physician to balance efficacy and tolerability.
Strength: 50mg
Pack Size: 20s
Storage: 2°C to 8°C (refrigerate); do not freeze
Form: Capsule

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Indications & Clinical Uses

  • Vepesid 50 mg capsules: the Vepesid brand is listed as discontinued by Drugs.com, although DailyMed still carries a label under the VePesid name, packaged by Amneal Pharmaceuticals NY LLC (effective 15 May 2026) and not naming Bristol Myers Squibb; this is a commercial status and no formal revocation of approval was found in the sources checked.
  • Each capsule contains etoposide, a topoisomerase II inhibitor chemotherapy medicine, approved in the US in combination with other approved chemotherapy as first-line treatment of small cell lung cancer.
  • It is prescribed under supervision of a physician experienced in cancer chemotherapy.
  • The oral dose is twice the intravenous dose, rounded to the nearest 50 mg, so capsules must not be confused with etoposide injection.
  • Safety and effectiveness in children have not been established.

Side Effects

  • BOXED WARNING: severe myelosuppression with resulting infection or bleeding may occur.
  • Low white blood cells (below 4,000 per mm3) occur in 60% to 91% of patients and low platelets (below 100,000 per mm3) in 22% to 41%.
  • Nausea and vomiting affect 31% to 43%, hair loss 8% to 66%, sometimes progressing to total baldness but reversible, loss of appetite 10% to 13% and diarrhoea 1% to 13%.
  • Allergic or anaphylactic-like reactions occur in roughly 1% to 2% overall (under 1% with the oral form).
  • Acute leukaemia has been reported rarely and etoposide is considered a potential carcinogen.
  • Report fever, chills, unusual bruising or bleeding, or breathing difficulty immediately.

Precautions & Warnings

  • Frequent blood counts are required because bone marrow suppression is dose-limiting; doses may need to be modified after prior radiation or chemotherapy, or if serum albumin is low.
  • Etoposide is contraindicated in people with previous hypersensitivity to it or to any component.
  • It can cause fetal harm (Pregnancy Category D) and women of childbearing potential should avoid becoming pregnant.
  • It is not known whether etoposide passes into breast milk, and a decision must be made whether to stop nursing or the drug.
  • The dose is reduced to 75% when creatinine clearance is 15 to 50 mL/min.
  • Safety and effectiveness in children have not been established.
  • Store capsules in a refrigerator at 2°C to 8°C and do not freeze; they are stable for 24 months refrigerated.

Avoid Interactions

  • Cyclosporin A at high concentrations (above 2,000 ng/mL) taken with oral etoposide increased etoposide exposure by 80% and reduced its clearance by 38%, which raises the risk of toxicity, so this combination needs specialist supervision.
  • Other medicines that suppress the bone marrow, and previous radiation therapy or chemotherapy, can add to the blood-count effects, and doses are adjusted for them.
  • The label reviewed does not list food or alcohol restrictions or medicines that reduce etoposide's effect.
  • Tell your oncology team and pharmacist about every prescription medicine, over-the-counter product and supplement you take, and do not start any new one without checking first.

References

Frequently Asked Questions

Vepesid (etoposide) capsules are used with other approved chemotherapy as first-line treatment of small cell lung cancer. The brand is listed as discontinued by Drugs.com, though a VePesid label remains on DailyMed. Treatment must be supervised by a doctor experienced in cancer chemotherapy.

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