Prescription medication · Antiparasitic (Benzimidazole)

albendazole

Also sold as Albenza. Albendazole treats infections caused by tapeworms.

Data updated 2026-05-15

1,829
FDA reportsRarely reported
5
InteractionsFew interactions
$7.16
Generic price (NADAC)

What the data shows

albendazole (Albenza) is a prescription Antiparasitic (Benzimidazole), among the least-reported drugs the FDA tracks (1,829 FDA reports), with 5 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.

albendazole (Albenza) is a prescription Antiparasitic (Benzimidazole). Albendazole treats infections caused by tapeworms.

Albendazole is a medicine that fights parasites. It is used to treat infections caused by tapeworms.

Drug Pricing (NADAC)

Generic Price

$7.16/unit

Generic Available

Yes (5 manufacturers)

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

NADAC price trail: ALBENDAZOLE 200 MG TABLET

Same CMS presentation as the headline generic unit price above (2 effective dates). Adjacent % compares consecutive NADAC releases for this description only, not a patient out-of-pocket quote. Latest step: -1.6% vs prior release.

Effective NADAC / unit vs prior NDCs
July 17, 2024 $7.28/EA - 1
December 18, 2024 $7.16/EA -1.6% 5
View Alternatives → Compare with Another Drug → Full Side Effects Report →

What it does

Albendazole treats infections caused by tapeworms.

Common side effects

Abnormal liver function tests, Abdominal pain, Nausea

Key warnings

Albendazole can cause bone marrow suppression, which can be fatal.

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

How It Works

Albendazole stops the tapeworms from growing and multiplying. It does this by blocking the worm's ability to use sugar (glucose). This eventually kills the parasite.

Side Effects (from patient reports)

Based on 1,829 FDA adverse event reports.

Most-reported reactions

Adverse reactions in FAERS for albendazole, 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 albendazole each year to the FDA Adverse Event Reporting System (FAERS).

050100150200 20042007201020132016201920222025 168

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

Where albendazole sits

albendazole has more FDA adverse-event reports than 11% 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 albendazole; the line is the median (50th percentile).

FDA Adverse Event Report Analysis

Detailed analysis of 1,829 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 2004–2025.

Total Reports

1,829

Reports Mentioning Death

302

16.5% of reports — not proof of cause

Hospitalization Reports

658

Top Indication

Product Used For Unknown Indication

Gender Distribution

Female 758 (47%)
Male 860 (53%)

Age Distribution

0–17 226
18–44 466
45–64 518
65–74 143
75+ 68

Most Reported Adverse Reactions (FAERS)

# Reaction Reports
3 PYREXIA 236
5 HEADACHE 222
6 CONDITION AGGRAVATED 213
7 FATIGUE 167
8 WEIGHT DECREASED 166
9 RASH 165
10 PAIN 164
11 SOMNOLENCE 159
12 HAEMATOCHEZIA 157
13 RECTAL HAEMORRHAGE 149
14 COLITIS ULCERATIVE 148
15 STRESS 148
16 INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION 147
18 STEROID DEPENDENCE 147
19 BRONCHIECTASIS 146

Reactions in Death Reports

DEATH 64
STRONGYLOIDIASIS 44
PYREXIA 33
SEPSIS 28
RESPIRATORY FAILURE 26
SEPTIC SHOCK 25
DIARRHOEA 24
VOMITING 20
ANAEMIA 17
CONDITION AGGRAVATED 17

Reactions in Hospitalization Reports

PYREXIA 90
VOMITING 75
HEADACHE 62
ASTHENIA 60
STRONGYLOIDIASIS 54
CONDITION AGGRAVATED 52
DIARRHOEA 47
SOMNOLENCE 33
ABDOMINAL PAIN 31
DEHYDRATION 29

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

Serious Warnings

Albendazole can cause bone marrow suppression, which can be fatal. Your doctor will check your blood counts before and during treatment. If your blood counts drop too low, you may need to stop taking albendazole. Albendazole can also harm an unborn baby, so women who can get pregnant should use birth control while taking it. If you are being treated for neurocysticercosis, you may experience seizures or other neurological problems. Your doctor may give you steroids and anti-seizure medicine to prevent these problems.

Known Drug Interactions

( 7.3 ) Theophylline: Albendazole induces cytochrome P450 1A in human hepatoma cells; therefore, it is recommended that plasma concentrations of theophylline be monitored during and after treatment. 7.4 Theophylline Following a single dose of albendazole (400 mg), the pharmacokinetics of theophylline (aminophylline 5.8 mg/kg infused over 20 minutes) were unchanged. Albendazole induces cytochrome P450 1A in human hepatoma cells; therefore, it is recommended that plasma concentrations of theophylline be monitored during and after treatment.

Mechanism: Albendazole can make your liver work faster to clear theophylline from your body, which could make the theophylline less effective.

( 7.2 ) Cimetidine: Increased albendazole sulfoxide concentrations in bile and cystic fluid by about 2-fold in hydatid cyst patients. 7.3 Cimetidine Albendazole sulfoxide concentrations in bile and cystic fluid were increased (about 2-fold) in hydatid cyst patients treated with cimetidine (10 mg/kg/day) (n = 7) compared with albendazole (20 mg/kg/day) alone (n = 12).

Mechanism: Cimetidine interferes with how the body breaks down albendazole, which causes the drug levels to rise in certain body fluids.

7 DRUG INTERACTIONS Dexamethasone: Steady-state trough concentrations of albendazole sulfoxide were about 56% higher when dexamethasone was coadministered with each dose of albendazole. ( 5.5 , 7.4 ) 7.1 Dexamethasone Steady-state trough concentrations of albendazole sulfoxide were about 56% higher when 8 mg dexamethasone was co-administered with each dose of albendazole (15 mg/kg/day) in 8 neurocysticercosis patients.

Mechanism: Dexamethasone increases the amount of the active form of albendazole that stays in your bloodstream.

In addition, carbamazepine causes, or would be expected to cause, decreased levels of the following drugs, for which monitoring of concentrations or dosage adjustment may be necessary: acetaminophen, albendazole, alprazolam, aprepitant, buprenorphone, bupropion, citalopram, clonazepam, clozapine, corticosteroids (e.g., prednisolone, dexamethasone), cyclosporine, dicumarol, dihydropyridine calcium channel blockers (e.g., felodipine), doxycycline, ethosuximide, everolimus, haloperidol, imatinib, itraconazole, lamotrigine, levothyroxine, methadone, methsuximide, mianserin, midazolam,...

Mechanism: Carbamazepine speeds up the way your body clears out albendazole. This means there may not be enough albendazole in your blood to treat your infection effectively.

Phenytoin when given with the combination of fosamprenavir and ritonavir may increase the concentration of amprenavir Calcium channel blockers Nifedipine, nimodipine, nisoldipine, verapamil Other Albendazole (decreases active metabolite), chlorpropamide, clozapine, cyclosporine, digoxin, disopyramide, folic acid, methadone, mexiletine, praziquantel, quetiapine a The effect of phenytoin on phenobarbital, valproic acid and sodium valproate serum levels is unpredictable 7.3 Drug/Laboratory Test Interactions Care should be taken when using immunoanalytical methods to measure serum phenytoin...

Mechanism: Phenytoin causes your body to process albendazole faster, which reduces the amount of the active medicine available to fight infection.

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

Common Questions

Can I take albendazole without food?
No, you should always take albendazole with food.
How long will I need to take albendazole?
The length of treatment depends on the type of infection you have. For hydatid disease, it is usually given in 28-day cycles with breaks in between. For neurocysticercosis, it can be taken for 8 to 30 days.
What should I do if I experience side effects?
Tell your doctor about any side effects you experience while taking albendazole.
Will albendazole interact with other medications I am taking?
Albendazole can interact with other medications, such as dexamethasone, praziquantel, cimetidine, and theophylline. Tell your doctor about all the medications you are taking.
Can I drink alcohol while taking albendazole?
Ask your doctor if it is safe to drink alcohol while taking albendazole.
What tests will I need while taking albendazole?
Your doctor will monitor your blood counts and liver enzymes before and during treatment.
Can I breastfeed while taking albendazole?
It is not known if albendazole passes into breast milk. Talk to your doctor before breastfeeding.
What if I can't swallow the tablet?
You can crush or chew the albendazole tablets and swallow them with a drink of water.
Is there a generic version of albendazole?
Yes, albendazole is available as a generic medication.
How soon will I feel better after starting albendazole?
It may take several days or weeks before you start to feel better. Continue taking albendazole as prescribed by your doctor.
What are the common side effects of albendazole?
The registry lists Abnormal liver function tests, Abdominal pain, Nausea, Vomiting, Reversible hair loss among the most-reported FAERS reaction terms for albendazole. The compiled record contains 1,829 FDA adverse-event reports. These counts are not an individual symptom assessment.
Does albendazole interact with other medications?
The registry has 5 documented interaction rows for albendazole. Notable source-record pairings include theophylline, cimetidine, dexamethasone. These rows are not a complete medication review.
What drug class is albendazole?
albendazole belongs to the Antiparasitic (Benzimidazole) drug class. It requires a prescription (Rx). Albendazole treats infections caused by tapeworms.
What pregnancy or breastfeeding source fields are listed for albendazole?
The FDA label for albendazole contains product-specific pregnancy or breastfeeding language. PlainMeds does not apply that source text to an individual.

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

Compare albendazole vs acyclovir side-by-side →

Compare beyond drug class

Nationwide peers by FAERS volume & death-report share

Two PlainMeds-derived comparison paths for albendazole: 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 albendazole

The FDA label for albendazole (sold under brand names such as Albenza) classifies it as a prescription-only medication in the Antiparasitic (Benzimidazole) class. Albendazole treats infections caused by tapeworms. Official labeling lists 10 commonly reported side effects, including Abnormal liver function tests, Abdominal pain, Nausea.

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 1,829 voluntary reports. The database also lists 5 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 $7.16.

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: September 30, 2019

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