Acamprosate Dosing for Alcohol Dependence
The recommended dose of acamprosate is 666 mg (two 333 mg tablets) three times daily for patients weighing ≥60 kg, with dose reduction to one-third less (1332 mg daily total) for patients weighing <60 kg. 1
Standard Dosing Algorithm
For patients ≥60 kg:
- 666 mg (two 333 mg tablets) three times daily
- Total daily dose: 1998 mg 1
For patients <60 kg:
- Reduce dose by one-third
- 1332 mg daily total (typically 333 mg tablets, dosing adjusted accordingly) 2
For moderate renal impairment (CrCl 30-50 mL/min):
For severe renal impairment (CrCl ≤30 mL/min):
- Acamprosate is contraindicated 1
Critical Timing Considerations
Acamprosate must be initiated 3-7 days after the last alcohol consumption and only after withdrawal symptoms have completely resolved. 2 Starting too early reduces efficacy since acamprosate maintains abstinence rather than induces it. 3, 2
The FDA label confirms treatment should be initiated "as soon as possible after the period of alcohol withdrawal, when the patient has achieved abstinence." 1
Treatment Duration
- Typical treatment period: 3-6 months 2
- Can extend up to 12 months for optimal results 2
- Continue treatment even if patient relapses 1
Administration Details
- Dosing may be done without regard to meals, though dosing with meals was used in clinical trials and is suggested for patients who regularly eat three meals daily 1
- Steady-state plasma concentrations are reached after 5-7 days of repeated dosing 4
- The enteric-coated formulation should not be crushed 1
Essential Caveats
Acamprosate is not effective for inducing abstinence or treating acute withdrawal. 3 Patients must be detoxified first, with a number needed to treat of 12 to prevent relapse. 3
Must be combined with comprehensive psychosocial treatment programs - using acamprosate without psychosocial support is a common pitfall that reduces efficacy. 3, 2, 1
Safety Profile Advantages
Acamprosate is particularly safe for patients with liver disease as it carries no risk of hepatotoxicity and is not metabolized by the liver. 3, 2 This makes it the preferred agent in patients with alcohol-associated liver disease according to the American Association for the Study of Liver Diseases. 3
The most common adverse effect is diarrhea, which is generally mild and transient. 1, 5