Etoposide
Podophyllotoxin Derivatives
Sold as VEPESID
- Drug class
- Podophyllotoxin Derivatives
- Availability
- Prescription only
- Routes
- Intravenous, Oral
- Markets covered
- 3
- Products on record
- 15
- FDA reports (12 mo)
- 4,599
Overview
Etoposide is an active pharmaceutical ingredient in the Podophyllotoxin Derivatives group (L01CB). The information below is compiled per regulator from the product labels on record, with direct links to the original documents.
Regulatory status by market
| Market | Regulator | Products | Last revision |
|---|---|---|---|
| GB United Kingdom | MHRA | 10 | May 15, 2026 |
| CA Canada | Health Canada | 3 | April 2, 2026 |
| US United States | FDA | 2 | May 20, 2026 |
GBUnited Kingdom· MHRA
10 products
Uses
Testicular cancer Etoposide is indicated in combination with other approved chemotherapeutic agents for the treatment of first line, recurrent or refractory testicular cancer in adults. Small cell lung cancer Etoposide is indicated in combination with other approved chemotherapeutic agents for the treatment of small-cell lung cancer in adults.
Hodgkin’s lymphoma Etoposide is indicated in combination with other approved chemotherapeutic agents for the treatment of Hodgkin’s lymphoma in adult and paediatric patients. Non-Hodgkin’s lymphoma Etoposide is indicated in combination with other approved chemotherapeutic agents for the treatment of non-Hodgkin’s lymphoma in adult and paediatric patients.
Acute myeloid leukaemia Etoposide is indicated in combination with other approved chemotherapeutic agents for the treatment of acute myeloid leukaemia in adult and paediatric patients. Gestational trophoblastic neoplasia Etoposide is indicated for first line and second line therapy in combination with other approved chemotherapeutic agents for the treatment of high risk gestational trophoblastic neoplasia in adults.
CACanada· Health Canada
3 products
Uses
VEPESID (etoposide) is indicated for:
Small Cell Carcinoma of the Lung • first-line therapy in combination with other established antineoplastic agents. • second-line combination or single agent therapy in patients who have not responded or relapsed on other chemotherapeutic regimens.
Malignant Lymphoma (histiocytic type) • first-line therapy in combination with other established antineoplastic agents. Non-small Cell Carcinoma of the Lung • for patients considered ineligible for surgery, etoposide has been shown effective alone or in combination with PLATINOL (cisplatin).
• for patients who require chemotherapy following surgery. Testicular Malignancies (germ cell tumours including seminomas) • in combination with other effective chemotherapeutic agents in patients who have already received appropriate therapy.
1 Pediatrics Pediatrics(<18 years of age): No data are available to Health Canada; therefore, Health Canada has not authorized an indication for pediatric use. 2 Geriatrics Geriatrics: No data are available to Health Canada; therefore, Health Canada has not authorized an indication for geriatric use.
USUnited States· FDA
2 products
Uses
INDICATIONS AND USAGE
Etoposide Injection is indicated in the management of the following neoplasms:
Refractory Testicular Tumors Etoposide Injection in combination therapy with other approved chemotherapeutic agents in patients with refractory testicular tumors who have already received appropriate surgical, chemotherapeutic, and radiotherapeutic therapy.
Small Cell Lung Cancer Etoposide Injection and/or capsules in combination with other approved chemotherapeutic agents as first line treatment in patients with small cell lung cancer.
How to take
Drug interactions
Known interactions involving Etoposide. Select one for details. This list is informational and not a complete interaction checker.
Showing 240 of 446. Type above to find a specific drug.
Interaction data compiled from DDInter (academic, CC-BY). Severity classification only - this is not a complete interaction checker and not medical advice.
Sources & citations
- [1]MHRA (UK) · PL088280293 · revised May 15, 2026
- [2]Health Canada (DPD) · 00616192 · revised March 22, 2025
- [3]FDA DailyMed · 0dddbe44-b4f4-43… · revised May 20, 2026 [PDF]
- [4]OpenFDA adverse-event reports (US), 12 months ending June 4, 2026.
Information on this page is compiled from public regulatory records. Drugvu is not affiliated with any regulator or pharmaceutical manufacturer. This is not medical advice. Always consult a qualified healthcare professional.