Prescription medication · GABA Analog (Alcohol Dependence)

acamprosate

Also sold as Campral. Acamprosate helps people who are alcohol-dependent to not drink alcohol.

Data updated 2026-05-15

299
FDA reportsRarely reported
3
InteractionsFew interactions
$0.36
Generic price (NADAC)

What the data shows

acamprosate (Campral) is a prescription GABA Analog (Alcohol Dependence), among the least-reported drugs the FDA tracks (299 FDA reports), with 3 documented drug interactions.

Reporting volume reflects how widely a drug is used and studied, not how dangerous it is, a FAERS report documents a temporal association, never proof of cause.

acamprosate (Campral) is a prescription GABA Analog (Alcohol Dependence). Acamprosate helps people who are alcohol-dependent to not drink alcohol.

Acamprosate is a medicine that can help you stay away from alcohol if you are alcohol-dependent and have already stopped drinking. It should be used with counseling and support.

Drug Pricing (NADAC)

Generic Price

$0.36/unit

Generic Available

Yes (4 manufacturers)

Pricing data from NADAC (CMS), effective December 18, 2024. Compare all drug costs →

Compare with Another Drug → Full Side Effects Report →

What it does

Acamprosate helps people who are alcohol-dependent to not drink alcohol.

Common side effects

Accidental injury, Weakness, Pain

Key warnings

Acamprosate may increase the risk of suicidal thoughts or actions.

The sections below are summarized in plain English from acamprosate's FDA-approved prescribing information. They describe what the official label says, and are not personal medical advice.

How It Works

Acamprosate is similar to a natural substance in your brain. It is thought to work by helping to restore the normal balance of brain activity that is changed by long-term alcohol use. This can reduce your craving for alcohol.

Side Effects (from patient reports)

Based on 299 FDA adverse event reports.

Most-reported reactions

Adverse reactions in FAERS for acamprosate, by number of reports

reports

What this shows Bars show how often each reaction was reported, not how likely it is to happen, a report records a temporal association, never proof that the drug caused it.

Source FDA Adverse Event Reporting System (FAERS) As of 2025

Reports over time

Adverse-event reports filed for acamprosate each year to the FDA Adverse Event Reporting System (FAERS).

0204060 2006201020142017202020232025 52

Year-to-year volume tracks usage, prescribing, and scrutiny, not a change in per-patient risk. Source: FDA FAERS.

Where acamprosate sits

acamprosate has more FDA adverse-event reports than 2% of the drugs FAERS tracks. A high position reflects how widely a drug is used and watched, not how dangerous it is.

fewest reports most reports

Percentile across all drugs PlainMeds tracks by FAERS report volume. The dot is acamprosate; the line is the median (50th percentile).

FDA Adverse Event Report Analysis

Detailed analysis of 299 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 2006–2025.

Total Reports

299

Reports Mentioning Death

25

8.4% of reports — not proof of cause

Hospitalization Reports

144

Top Indication

Product Used For Unknown Indication

Gender Distribution

Female 108 (40%)
Male 159 (60%)

Age Distribution

18–44 67
45–64 113
65–74 42
75+ 2

Most Reported Adverse Reactions (FAERS)

# Reaction Reports
1 HYPOTENSION 14
2 ASTHENIA 13
3 CONDITION AGGRAVATED 13
5 ACUTE KIDNEY INJURY 12
6 COMA 12
7 FATIGUE 11
8 TOXICITY TO VARIOUS AGENTS 11
9 DRUG ABUSE 10
10 HEADACHE 10
11 BRADYCARDIA 9
12 CYTOLYTIC HEPATITIS 9
13 DEPRESSION 9
14 HEPATIC CYTOLYSIS 9
15 HYPOGLYCAEMIA 9
16 NEUTROPENIA 9

Reactions in Death Reports

TOXICITY TO VARIOUS AGENTS 8
COMPLETED SUICIDE 6
DEATH 5
INTERSTITIAL LUNG DISEASE 3
CARDIAC ARREST 2
GASTROINTESTINAL HAEMORRHAGE 2
ASPHYXIA 1
CARDIO-RESPIRATORY ARREST 1
CIRCULATORY COLLAPSE 1
DRUG TOXICITY 1

Reactions in Hospitalization Reports

ACUTE KIDNEY INJURY 12
CONDITION AGGRAVATED 11
COMA 10
CYTOLYTIC HEPATITIS 9
DRUG ABUSE 9
HYPOGLYCAEMIA 9
HYPOTENSION 9
OVERDOSE 9
ATRIOVENTRICULAR BLOCK 8
BRADYCARDIA 8

Source: FDA FAERS (Adverse Event Reporting System) Reports are voluntary and do not establish causation

Serious Warnings

Acamprosate may increase the risk of suicidal thoughts or actions. Your doctor should watch you for depression or suicidal thoughts. Tell your doctor right away if you have any new or worsening symptoms of depression or suicidal thoughts.

Known Drug Interactions

The pharmacokinetics of acamprosate are not affected by alcohol, diazepam, or disulfiram, and clinically important interactions between naltrexone and acamprosate were not observed [ see Clinical Pharmacology (12.3) ].

Mechanism: Diazepam does not change the way your body absorbs or uses acamprosate. These drugs do not have a known interaction that affects their levels in the blood.

The pharmacokinetics of acamprosate are not affected by alcohol, diazepam, or disulfiram, and clinically important interactions between naltrexone and acamprosate were not observed [ see Clinical Pharmacology (12.3) ].

Mechanism: These two drugs do not significantly change how the other works in your body.

The pharmacokinetics of acamprosate are not affected by alcohol, diazepam, or disulfiram, and clinically important interactions between naltrexone and acamprosate were not observed [ see Clinical Pharmacology (12.3) ].

Mechanism: Disulfiram does not change the way your body breaks down or uses acamprosate.

This is a plain-language summary of FDA-label interaction records and does not provide individual medication-combination directions.

Common Questions

Can I drink alcohol while taking acamprosate?
No, acamprosate is meant to help you maintain abstinence from alcohol. It will not prevent withdrawal symptoms if you drink alcohol.
What if I have kidney problems?
If you have moderate kidney problems, your doctor may prescribe a lower dose. If you have severe kidney problems, you should not take acamprosate.
Will acamprosate cure my alcoholism?
No, acamprosate helps reduce cravings and maintain abstinence, but it is not a cure. It should be used with counseling and support.
How long will I need to take acamprosate?
Your doctor will determine how long you should take acamprosate. It is important to follow your doctor's instructions.
Can I stop taking acamprosate suddenly?
Talk to your doctor before stopping acamprosate. Stopping suddenly may affect your treatment.
Does acamprosate interact with other medications?
Acamprosate does not have many known drug interactions, but always tell your doctor about all the medicines you take.
What should I do if I feel depressed or suicidal?
Tell your doctor right away if you have any new or worsening symptoms of depression or suicidal thoughts.
Can I drive or operate machinery while taking acamprosate?
Acamprosate may cause dizziness. Be careful driving or operating machinery until you know how it affects you.
What are the ingredients in acamprosate?
The active ingredient is acamprosate calcium. Inactive ingredients include colloidal anhydrous silica, methacrylic acid copolymer type c, and others.
How should I dispose of unused acamprosate?
Ask your pharmacist about how to properly dispose of unused medication.
What are the common side effects of acamprosate?
The registry lists Accidental injury, Weakness, Pain, Loss of appetite, Diarrhea among the most-reported FAERS reaction terms for acamprosate. The compiled record contains 299 FDA adverse-event reports. These counts are not an individual symptom assessment.
Does acamprosate interact with other medications?
The registry has 3 documented interaction rows for acamprosate. Notable source-record pairings include diazepam, naltrexone, disulfiram. These rows are not a complete medication review.
What drug class is acamprosate?
acamprosate belongs to the GABA Analog (Alcohol Dependence) drug class. It requires a prescription (Rx). Acamprosate helps people who are alcohol-dependent to not drink alcohol.
What pregnancy or breastfeeding source fields are listed for acamprosate?
The FDA label for acamprosate contains product-specific pregnancy or breastfeeding language. PlainMeds does not apply that source text to an individual.

Other drugs grouped near acamprosate - same-class peers and common alternatives.

Compare acamprosate vs alprazolam side-by-side →

Compare beyond drug class

Nationwide peers by FAERS volume & death-report share

Two PlainMeds-derived comparison paths for acamprosate: nearest FDA FAERS report volume and nearest death-report share among drugs with at least 1,000 logged reports, excluding same-class neighbors listed above. Counts reflect reporting volume, not proven individual harm.

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What the FDA Data Shows for acamprosate

The FDA label for acamprosate (sold under brand names such as Campral) classifies it as a prescription-only medication in the GABA Analog (Alcohol Dependence) class. Acamprosate helps people who are alcohol-dependent to not drink alcohol. Official labeling lists 15 commonly reported side effects, including Accidental injury, Weakness, Pain.

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 299 voluntary reports. The database also lists 3 documented drug interactions derived from FDA labeling, with the top-flagged interaction rated minor severity. NADAC pricing from CMS shows a generic unit cost of $0.36.

Report counts do not establish causation, a FAERS entry documents a temporal association, not proof that the drug produced the outcome. Widely prescribed medications naturally accumulate more reports than niche therapies, so raw totals must be interpreted alongside total exposure. Shortage status, recall history, and patent information are separate source-record fields. This page is a public FDA/CMS registry and does not provide medical, treatment, substitution, or medication-change directions.

Data Sources

Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS). Pricing: CMS National Average Drug Acquisition Cost (NADAC).

FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. This registry does not provide medication decisions.

Last updated: November 6, 2023

PlainMeds is rendered directly from FDA openFDA/FAERS extracts, DailyMed labels, and CMS drug-pricing files, no number is typed in by an editor. FAERS counts, recalls, shortages, and price figures on this page are queried live from those federal extracts. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of 2026-05-15. Primary sources: openFDA / FAERS, DailyMed and CMS Part B ASP.

Data currency: FDA FAERS adverse-event reports through 2025, CMS NADAC acquisition-cost pricing effective December 2024, compiled from the source snapshot dated . See our methodology for per-source dates and refresh cadence. Spot a figure that looks wrong? Report a data issue.

All federal data sources used on this page