Aldehyde dehydrogenase inhibitor (aversion agent for alcohol use disorder)

Disulfiram

Antabuse
FDA-Approved Indications
  • Alcohol use disorder (adjunct to supportive and psychotherapeutic treatment in motivated patients)
Common Off-Label Uses
  • Cocaine use disorder (early-stage research based on dopamine beta-hydroxylase inhibition; not an established indication)

Side Effects Worth Knowing

Hepatotoxicity

The primary medical risk. Ranges from asymptomatic transaminase elevation to fulminant hepatic failure (rare but reported, including fatalities). Baseline LFTs required. Periodic monitoring (commonly every 3-6 months). Discontinue if significant elevation. Patients should report jaundice, dark urine, abdominal pain, unexplained fatigue.

Metallic or garlic-like taste

Frequently reported, usually mild. Can be persistent and bothersome.

Drowsiness/fatigue

Common at initiation. Usually improves with continued use. Bedtime dosing may help.

Headache

Usually mild and transient.

Skin eruptions

Acneiform eruptions and allergic dermatitis have been described.

Peripheral neuropathy

With prolonged use. Numbness, tingling, weakness in extremities. Monitor for neuropathic symptoms. Discontinue if neuropathy develops.

Optic neuritis

Rare. Visual changes warrant immediate discontinuation and ophthalmologic evaluation.

Psychiatric effects

Psychosis, depression, confusion, and personality changes have been reported, particularly at higher doses. The DBH inhibition (increased dopamine relative to norepinephrine) may contribute. Monitor mental status, particularly in patients with pre-existing psychiatric conditions.

The disulfiram-ethanol reaction

Not a side effect in the traditional sense, it is the therapeutic mechanism. But the severity spectrum includes potentially fatal outcomes. Patients must understand this before starting.

References & Further Reading

This page synthesizes information from standard clinical references. Consult primary sources for all prescribing decisions.

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For learning and board prep — not a prescribing reference. Dosing and safety information change. Always verify against current FDA labeling and your institution’s protocols before prescribing.