Mebendazole clinical pharmacology

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Mebendazole
MEBENDAZOLE® FDA Package Insert
Description
Clinical Pharmacology
Indications and Usage
Contraindications
Warnings and Precautions
Adverse Reactions
Drug Interactions
Overdosage
Dosage and Administration
How Supplied
Labels and Packages

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Clinical Pharmacology

Following administration of 100 mg twice daily for three consecutive days, plasma levels of mebendazole and its primary metabolite, the 2-amine, do not exceed 0.03 mcg/mL and 0.09 mcg/mL, respectively. All metabolites are devoid of anthelmintic activity. In man, approximately 2% of administered mebendazole is excreted in urine and the remainder in the feces as unchanged drug or a primary metabolite.

Mode of Action

Mebendazole inhibits the formation of the worms’ microtubules and causes the worms’ glucose depletion.[1]

References

  1. "MEBENDAZOLE TABLET, CHEWABLE [TEVA PHARMACEUTICALS USA INC]".

Adapted from the FDA Package Insert.