What are the clinically important drug interactions of mebendazole and how should they be managed?

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Mebendazole Drug Interactions

Cimetidine is the most clinically significant drug interaction with mebendazole, as it inhibits mebendazole metabolism and increases plasma concentrations, requiring dose monitoring when co-administered. 1

Primary Drug Interaction: Cimetidine

  • Cimetidine inhibits mebendazole metabolism, resulting in increased plasma concentrations and maximum concentration (Cmax) of mebendazole 1, 2
  • This interaction occurs through inhibition of hepatic metabolism pathways 2
  • Clinical management: Monitor for enhanced mebendazole effects and potential toxicity when these drugs are used together; consider alternative H2-blockers if possible 1

Anticonvulsant Interactions

  • Enzyme-inducing anticonvulsants (phenytoin, carbamazepine, phenobarbital) decrease mebendazole exposure by increasing hepatic metabolism 2
  • These interactions reduce the area under the plasma concentration-time curve (AUC) of mebendazole, potentially compromising efficacy 2
  • Clinical management: Consider using higher doses of mebendazole or alternative anthelmintics in patients on chronic anticonvulsant therapy 2

Antiretroviral Interactions

  • Ritonavir decreases the AUC of mebendazole through enzyme induction mechanisms 2
  • This interaction may reduce mebendazole efficacy in HIV-infected patients requiring anthelmintic therapy 2
  • Clinical management: Monitor treatment response closely and consider dose adjustments or alternative agents 2

Other Documented Interactions

Dexamethasone

  • Increases albendazole (related benzimidazole) exposure but specific mebendazole interaction data is limited 2
  • May theoretically affect mebendazole similarly given structural similarities 2

No Significant Interactions

  • Ivermectin, azithromycin, diethylcarbamazine, praziquantel, and levamisole show no major pharmacokinetic interactions with mebendazole when co-administered 2
  • These combinations can be safely used for polyparasitic infections 2

Hepatic Metabolism Considerations

  • Mebendazole has poor systemic absorption, which limits the clinical significance of many potential drug interactions 3
  • The drug's primary site of action is in the gastrointestinal tract, where it exerts its anthelmintic effects through microtubular destruction 3
  • Prolonged therapy (>14-28 days) may increase risk of hepatotoxicity, particularly when combined with other hepatotoxic agents 4

Monitoring Recommendations

  • Periodic assessment of hepatic function is advisable during prolonged mebendazole therapy, especially when combined with interacting medications 1
  • No routine therapeutic drug monitoring is typically required for short-term anthelmintic courses 1
  • Hematopoietic function monitoring should be considered during extended treatment periods 1

Special Populations

Pregnancy

  • Mebendazole is Pregnancy Category C and has shown embryotoxic and teratogenic effects in rats at doses approximately equal to human doses 1
  • Use is not recommended in pregnant women, particularly during the first trimester 1
  • Drug interactions become particularly relevant when considering alternative agents in pregnant patients 1

Pediatric Patients

  • The drug has not been extensively studied in children under 2 years of age 1
  • Drug interaction considerations should factor into the benefit/risk assessment in young children 1

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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