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MBDZ: Full Drug Profile

Medically reviewed by Min Clinic Staff | Updated: January 2026

MBDZ - General Information

A benzimidazole that acts by interfering with carbohydrate metabolism and inhibiting polymerization of microtubules. [PubChem]

 

Pharmacology of MBDZ

MBDZ is a (synthetic) broad-spectrum anthelmintic. The principal mode of action for albendazole is by its inhibitory effect on tubulin polymerization which results in the loss of cytoplasmic microtubules.

 

MBDZ for patients

Patients should be informed of the potential risk to the fetus in women taking VERMOX® (mebendazole) during pregnancy, especially during the first trimester.

Patients should also be informed that cleanliness is important to prevent reinfection and transmission of the infection.

 

MBDZ Interactions

Preliminary evidence suggests that cimetidine inhibits mebendazole metabolism and may result in an increase in plasma concentrations of mebendazole.

 

MBDZ Contraindications

VERMOX® (mebendazole) is contraindicated in persons who have shown hypersensitivity to the drug.

 

Additional information about MBDZ

MBDZ Indication

For the treatment of Enterobius vermicularis (pinworm), Trichuris trichiura (whipworm), Ascaris lumbricoides (common roundworm), Ancylostoma duodenale (common hookworm), Necator americanus (American hookworm) in single or mixed infections.

Mechanism Of Action
MBDZ causes degenerative alterations in the tegument and intestinal cells of the worm by binding to the colchicine-sensitive site of tubulin, thus inhibiting its polymerization or assembly into microtubules. The loss of the cytoplasmic microtubules leads to impaired uptake of glucose by the larval and adult stages of the susceptible parasites, and depletes their glycogen stores. Degenerative changes in the endoplasmic reticulum, the mitochondria of the germinal layer, and the subsequent release of lysosomes result in decreased production of adenosine triphosphate (ATP), which is the energy required for the survival of the helminth. Due to diminished energy production, the parasite is immobilized and eventually dies.
Drug Interactions
Ethotoin The hydantoin decreases the efficiency of mebendazole
Food Interactions
Take with food.
Generic Name
Mebendazole
Drug Category
Antinematodal Agents
Drug Type
Small Molecule; Approved
Other Brand Names containing Mebendazole
Bantenol; Besantin; Equivurm Plus; Lomper; MBDZ; MEBENDAZOLE, 99%; Mebendazole (JAN/USP); Mebendazole(USAN); Mebenoazole; Mebenvet; Mebex; Mebutar; Noverme; Ovitelmin; Pantelmin; Telmin; Vermicidin; Vermirax; Vermox; Vermox (TN); Verpanyl;
Absorption
Poorly absorbed (approximately 5 to 10%) from gastrointestinal tract. Fatty food increases absorption.
Toxicity (Overdose)
Acute oral toxicity (LD50): 620 mg/kg [Mouse]. Symptoms of overdose include elevated liver enzymes, headaches, hair loss, low levels of white blood cells (neutropenia), fever, and itching.
Protein Binding
90-95%
Biotransformation
Primarily hepatic. Primary metabolite is 2-amino-5-benzoylbenzimidazole, but also metabolized to inactive hydroxy and hydroxyamino metabolites. All metabolites are devoid of anthelmintic activity.
Half Life
2.5 to 5.5 hours (range 2.5 to 9 hours) in patients with normal hepatic function. Approximately 35 hours in patients with impaired hepatic function (cholestasis).
Dosage Forms of MBDZ
Tablet Oral
Chemical IUPAC Name
methyl N-[6-(benzoyl)-1H-benzimidazol-2-yl]carbamate
Chemical Formula
C16H13N3O3
Organisms Affected
Helminthic Microorganisms