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Isoniazid drug and food interactions
T H Self1, C R Chrisman, A M Baciewicz
1Department of Clinical Pharmacy, University of Tennessee, Memphis 38163, USA.
The American Journal of the Medical Sciences
|May 20, 1999
Summary
Isoniazid significantly impacts drug metabolism, leading to potential toxicity with medications like phenytoin and carbamazepine. It also affects drug-food interactions and carries a risk of hepatotoxicity, especially with acetaminophen.
Area of Science:
- Pharmacology
- Drug Metabolism
- Clinical Toxicology
Background:
- Isoniazid is a crucial medication for tuberculosis treatment.
- Drug interactions involving isoniazid can lead to adverse events and treatment complications.
- Understanding isoniazid's metabolic pathways is vital for patient safety.
Purpose of the Study:
- To comprehensively review documented and potential drug interactions associated with isoniazid.
- To elucidate the mechanisms underlying isoniazid-induced drug interactions.
- To highlight clinical implications and risks of isoniazid therapy.
Main Methods:
- Systematic review of clinical trials and case reports on isoniazid interactions.
- Analysis of pharmacokinetic and pharmacodynamic data related to isoniazid.
- Evaluation of isoniazid's effect on specific drug-metabolizing enzymes, including CYP2E1.
Main Results:
- Isoniazid increases serum concentrations and toxicity of phenytoin and carbamazepine.
- High doses of isoniazid potentiate the effects of theophylline and warfarin.
- Isoniazid inhibits metabolism of certain benzodiazepines and vitamin D, and affects drug-food interactions.
- Isoniazid exhibits a biphasic effect on CYP2E1, contributing to acetaminophen interactions and hepatotoxicity risk.
Conclusions:
- Isoniazid is a potent inhibitor of drug metabolism, necessitating careful patient monitoring.
- Clinically significant drug-drug and drug-food interactions are well-documented for isoniazid.
- Further research is expected to uncover additional isoniazid-related interactions and their mechanisms.