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VePesid Side Effects

Generic name: etoposide

Medically reviewed by Drugs.com. Last updated on Feb 23, 2024.

Note: This document contains side effect information about etoposide. Some dosage forms listed on this page may not apply to the brand name VePesid.

Applies to etoposide: intravenous powder for solution, intravenous solution. Other dosage forms:

Warning

Intravenous route (Solution)

Severe myelosuppression with resulting infection or bleeding may occur with etoposide.

Serious side effects of VePesid

Along with its needed effects, etoposide (the active ingredient contained in VePesid) may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.

Check with your doctor or nurse immediately if any of the following side effects occur while taking etoposide:

More common

Less common

Rare

Incidence not known

Other side effects of VePesid

Some side effects of etoposide may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects.

Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:

More common

This medicine often causes a temporary loss of hair. After treatment with etoposide has ended, normal hair growth should return.

For Healthcare Professionals

Applies to etoposide: intravenous powder for injection, intravenous solution, oral capsule.

Hematologic

Very common (10% or more): Myelosuppression (sometimes fatal), leukopenia, thrombocytopenia, neutropenia, anemia[Ref]

Gastrointestinal

Very common (10% or more): Abdominal pain, constipation, nausea, vomiting, anorexia, mucositis (including stomatitis and esophagitis)

Common (1% to 10%): Diarrhea

Rare (less than 0.1%): Dysphagia, dysgeusia[Ref]

Cardiovascular

Common (1% to 10%): Myocardial infarction, arrhythmia, transient systolic hypotension (following rapid IV administration), hypertension

Uncommon (0.1% to 1%): Cyanosis

Rare (less than 0.1%): Heart failure[Ref]

Hypersensitivity

Common (1% to 10%): Anaphylaxis (sometimes fatal)[Ref]

Dermatologic

Very common (10% or more): Alopecia, pigmentation

Common (1% to 10%): Rash, urticaria, pruritus

Rare (less than 0.1%): Stevens-Johnson syndrome, toxic epidermal necrolysis, radiation recall dermatitis, maculopapular rash[Ref]

Hepatic

Common (1% to 10%): Hepatotoxicity[Ref]

Other

Very common (10% or more): Asthenia, malaise

Frequency not reported: Fever[Ref]

Respiratory

Rare (less than 0.1%): Pulmonary fibrosis, interstitial pneumonitis, bronchospasm, dyspnea[Ref]

Immunologic

Frequency not reported: Infectious complications[Ref]

Metabolic

Frequency not reported: Tumor lysis syndrome (sometimes fatal) has been reported following the use of this drug in association with other chemotherapeutic drugs[Ref]

Nervous system

Very common (10% or more: Neurotoxicity (e.g., somnolence, fatigue)

Common (1% to 10%): Dizziness

Uncommon (0.1% to 1%): Peripheral neuropathy

Rare (less than 0.1%): Seizure (occasionally associated with allergic reactions), optic neuritis, cortical blindness transient, neurotoxicity (e.g., somnolence, fatigue)

Frequency not reported: Aftertaste[Ref]

Ocular

Rare (0.01% to 0.1%): Optic neuritis, transient cortical blindness[Ref]

Local

Common (1% to 10%): Extravasation (e.g., local soft tissue toxicity, swelling, pain, cellulitis, necrosis including skin necrosis), phlebitis

Oncologic

Common (1% to 10%): Acute leukemia

Frequency not reported: Acute promyelocytic leukemia[Ref]

References

1. Product Information. Vepesid (etoposide). Bristol-Myers Squibb. 2001;PROD.

2. Cerner Multum, Inc. UK Summary of Product Characteristics.

3. Cerner Multum, Inc. Australian Product Information.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Some side effects may not be reported. You may report them to the FDA.