Table 2.
Medication | Acamprosate | Disulfiram | Naltrexone | Gabapentin | Topiramate |
---|---|---|---|---|---|
FDA Approval for AUD? | Yes | Yes | Yes | No | No |
Indications and clinical pearls |
For maintenance of abstinence from alcohol for patients who have completed detoxification and are abstinent from alcohol before beginning acamprosate Preferred in patients with hepatic impairment |
For highly motivated patients who have completed detoxification Cravings are not reduced with disulfiram |
Reduces alcohol cravings; can reduce the number of drinks that a daily drinker consumes Monthly injectable formulation may be helpful for compliance |
Off label use: Moderate to severe alcohol use disorder May be helpful in mild alcohol withdrawal syndrome or patients with neuropathic pain |
Off label use: Alcohol use disorder |
Mechanism of action | Promotes balance between the excitatory and inhibitory neurotransmitters, glutamate and GABA | Disrupts the metabolism of alcohol by inhibiting enzyme aldehyde dehydrogenase causing an unpleasant physical reaction when combined with alcohol | Blocks opiate receptors that are involved in the rewarding effects of drinking and craving for alcohol | Calcium channel blocker and y-aminobutyric acid (GABA) modulator | Antagonizes excitatory neurotransmitters (glutamate) and decreases dopamine release in reward pathway |
Dosing Note: For older patients, recommended to start low and go slow with dosing, but can titrate based on response and tolerability |
666 mg PO TID 333 mg PO TID (for patients with renal impairment) |
Start 125 mg PO daily (must be abstinent from alcohol >12 h), increase to 250 mg daily after several days Maintenance usually 250–500 mg daily |
50 mg PO daily OR 380 mg IM (gluteal) q4 weeks Do not initiate therapy until patient is opioid-free for at least 7–10 days (by urinalysis). |
Start 300 mg PO daily and increase dose in increments of 300 mg every 1–2 days up to a target dose of 600 mg three times a day |
Start 25 mg PO daily and increase dose by 25 mg weekly Poor tolerability seen in patients on doses greater than 100 mg/day |
Common side effects | Diarrhea (dose related, transient), weakness, peripheral edema, insomnia, anxiety | Skin eruptions (e.g., acne, allergic dermatitis), drowsiness, fatigue, impotence, headache, metallic taste | Headache, nausea, somnolence, vomiting | Drowsiness, fatigue, dizziness, stomach upset, dry mouth |
Dose-related sedative effects (dizziness, drowsiness, fatigue) Stomach upset, decreased appetite, anorexia, weight reduction, increased anxiety, paresthesias |
Contraindications and older adult considerations | Because of elevated risk of diminished renal function in people aged >65, baseline and frequent renal function tests (q3–6 months) are important in this population |
Contraindicated in severe myocardial disease or coronary occlusion, psychoses, and in those with high levels of impulsivity, suicidality, and hypersensitivity to disulfiram or to other thiuram derivatives Risk of hepatic toxicity in otherwise healthy adults Counsel patient that any alcohol ingestion can result in reaction (e.g., cough syrups, mouthwash) |
Can precipitate opioid withdrawal Do not use in patients with hepatitis or other liver dysfunction |
Do not use in chronic kidney disease May cause respiratory depression in older adults Increased risk of falls due to somnolence Can exacerbate myasthenia gravis |
Extended-release formulation contraindicated with recent alcohol use (6 h prior or after dose) and patients with metabolic acidosis with concomitant metformin use Risk of weight loss and short and long-term cognitive impairment (even at low doses, i.e., ≤100 mg/day) makes it not a first line treatment for AUD in older adults |