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Gliadel Side Effects

Generic name: carmustine

Medically reviewed by Drugs.com. Last updated on Jan 4, 2024.

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

Applies to carmustine: intravenous powder for solution. Other dosage forms:

Warning

Intravenous route (Powder for Solution)

Carmustine causes suppression of marrow function (including thrombocytopenia and leukopenia), which may contribute to bleeding and overwhelming infections. Monitor blood counts, adjust dosage based on nadir, and do not administer a repeat course until blood counts recover. Carmustine causes dose-related pulmonary toxicity; patients receiving greater than 1400 mg/m(2) cumulative dose are at significantly higher risk. Delayed pulmonary toxicity can occur years after treatment and may result in death, particularly in patients treated in childhood.

Serious side effects of Gliadel

Along with its needed effects, medicines like carmustine (the active ingredient contained in Gliadel) can sometimes cause some unwanted effects such as blood problems, loss of hair, and other side effects; these are described below. Also, because of the way these medicines act on the body, there is a chance that they might cause other unwanted effects that may not occur until months or years after the medicine is used. These delayed effects may include certain types of cancer, such as leukemia. Discuss these possible effects with your doctor.

Serious side effects of Gliadel

Along with its needed effects, carmustine 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 carmustine:

More common

Less common

Rare

Incidence not known

Other side effects of Gliadel

Some side effects of carmustine 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:

Less common

For Healthcare Professionals

Applies to carmustine: implant device, intravenous powder for injection.

Respiratory

Common (1% to 10%): Pneumonia, pulmonary embolism

Frequency not reported: Pulmonary toxicity (IV formulation)[Ref]

Hematologic

Frequency not reported: Myelosuppression (IV formulation)[Ref]

Gastrointestinal

Very common (10% or more): Nausea, vomiting, constipation

Common (1% to 10%): Abdominal pain

Postmarketing reports: Diarrhea, anorexia[Ref]

Hepatic

Postmarketing reports: Increased transaminase, increased alkaline phosphatase, increased bilirubin[Ref]

Renal

Postmarketing reports: Progressive azotemia, decrease in kidney size, renal failure[Ref]

Cardiovascular

Postmarketing reports: Tachycardia, chest pain, Veno-occlusive disease[Ref]

Local

Frequency not reported: Administration reactions (IV formulation)

Postmarketing reports: Burning sensation[Ref]

Other

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

Common (1% to 10%): Chest pain

Frequency not reported: Wafer migration (wafer formulation)[Ref]

Ocular

Frequency not reported: Ocular toxicity (IV formulation)

Postmarketing reports: Conjunctival edema, conjunctival hemorrhage, blurred vision, loss of depth perception[Ref]

Oncologic

Postmarketing reports: Acute leukemia, bone marrow dysplasia[Ref]

Immunologic

Very common (10% or more): Impaired neurosurgical wound healing (wafer formulation) (16%)

Common (1% to 10%): Meningitis (wafer formulation)

Postmarketing reports: Opportunistic infection (sometimes fatal)

Musculoskeletal

Common (1% to 10%): Back pain

Metabolic

Postmarketing reports: Diabetes mellitus

Psychiatric

Very common (10% or more): Confusion, depression

Common (1% to 10%): Anxiety, thinking abnormal, hallucinations, insomnia, personality disorder

Genitourinary

Very common (10% or more): Urinary tract infection

Nervous system

(wafer formulation) (23%), aphasia, somnolence, speech disorder

Common (1% to 10%): Intracranial hypertension (wafer formulation), brain abscess (wafer formulation), brain cyst (wafer formulation), hydrocephalus (wafer formulation), cerebral edema (wafer formulation), amnesia, facial paralysis, ataxia, hypesthesia, paresthesia, abnormal gait, dizziness, tremor, coma, hypokinesia

Postmarketing reports: Headache, encephalopathy

Dermatologic

Very common (10% or more): Rash

Postmarketing reports: Hyperpigmentation, swelling, erythema, skin necrosis, alopecia, allergic reaction

References

1. Multum Information Services, Inc. Expert Review Panel

2. O'Driscoll BR, Kalra S, Gattamaneni HR, Woodcock AA. Late carmustine lung fibrosis. Age at treatment may influence severity and survival. Chest. 1995;107:1355-7.

3. Lena H, Desrues B, Le Coz A, Quinquenel ML, Delaval P. Severe diffuse interstitial pneumonitis induced by carmustine (BCNU). Chest. 1994;105:1602-3.

4. Hasleton PS, O'Driscoll BR, Lynch P, Webster A, Kalra SJ, Gattamaneini HR, Woodcock AA, Poulter LW. Late BCNU lung: a light and ultrastructural study on the delayed effect of BCNU on the lung parenchyma. J Pathol. 1991;164:31-6.

5. Product Information. BiCNU (carmustine). Bristol-Myers Squibb. 2001;PROD.

6. Kanj SS, Sharara AI, Shpall EJ, Jones RB, Peters WP. Myocardial ischemia associated with high-dose carmustine infusion. Cancer. 1991;68:1910-2.

7. Mrozek-Orlowski M, Christie J, Flamme C, Novak J. Pain associated with peripheral infusion of carmustine. Oncol Nurs Forum. 1991;18:942.

8. Wiencke JK, Wiemels J. Genotoxicity of 1,3-bis(2-chloroethyl)-1-nitrosourea (BCNU). Mutat Res. 1995;339:91-119.

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.