Plain language summary

Disulfiram (Antabuse) is a medication that causes an unpleasant reaction if alcohol is consumed, helping people stay alcohol-free by removing the option to drink safely. This card is a prescribing reference for doctors. If you are a patient, your doctor will explain whether it is suitable for you.

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Medication Reference Card — Alcohol Use Disorder

Disulfiram (Antabuse)

200–500 mg/day orally · Requires alcohol-free ≥24 h before initiation · Not PBS-listed (full cost to patient)

Dr Basanth Kenchaiah
FRANZCP · MBBS · DPM · DNB (Psychiatry) · Cert. Addiction Psych. Addiction Psychiatrist v1.0 · May 2026
Audience Clinicians
Purpose Prescribing quick-reference for disulfiram (Antabuse) in alcohol use disorder (AUD).
Key messages
  • Aldehyde dehydrogenase inhibitor — causes aversive flushing/nausea/tachycardia if alcohol is consumed
  • 200 mg/day standard dose; supervised administration strongly preferred to ensure adherence and safety
  • Contraindicated in severe cardiac or hepatic disease, psychosis, and concurrent metronidazole or isoniazid

For Patients

Disulfiram works by causing an unpleasant physical reaction — flushing, nausea, and palpitations — if alcohol is consumed. This creates a strong deterrent. It works best when taken under supervision and when a person is highly motivated to stop drinking.

Particularly useful when comorbid with:
Cocaine use disorder (dopamine-beta-hydroxylase inhibition) Supervised administration available (partner / pharmacist / GP) Short-term commitment to abstinence (professional / legal obligations) Deterrence-based motivation profile

For Clinicians

Mechanism

Inhibits aldehyde dehydrogenase, causing toxic accumulation of acetaldehyde after alcohol ingestion → flushing, tachycardia, nausea, vomiting, hypotension (disulfiram-ethanol reaction / DER). Also inhibits dopamine beta-hydroxylase — basis for cocaine use disorder effect.

Dosing

Maintenance: 200 mg/day orally (range 200–500 mg/day). Patient must be alcohol-free for at least 24 hours before initiation. DER risk persists up to 14 days after last dose — counsel patients clearly. Supervised dosing (partner, pharmacist, GP) significantly improves efficacy.

Evidence

No statistically significant benefit over placebo in double-blind RCTs (Fuller et al. JAMA 1986). Strong evidence only in supervised/observed administration settings. Cochrane-level meta-analysis (Skinner et al. PLoS One 2014) confirms supervised disulfiram superior to naltrexone and acamprosate for abstinence days when compliance is assured.

Cautions
  • Contraindicated: severe cardiac disease, psychosis, significant impulsivity, pregnancy
  • Avoid with metronidazole (psychotic reaction), paraldehyde, amitriptyline
  • Hepatotoxicity risk — baseline LFTs, repeat at 2 weeks; avoid if ALT/AST >3× ULN
  • Drug interactions: warfarin (↑INR — monitor closely), phenytoin (↑levels)
  • DER can be severe — ensure patient understands hidden alcohol in medications, foods, mouthwash