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Related Concept Videos

Antiepileptic Drugs: Potassium Channel Activators01:20

Antiepileptic Drugs: Potassium Channel Activators

Ezocgabine or retigabine, an antiepileptic drug of remarkable efficacy, has revolutionized the management of seizures. It is a potassium channel activator, explicitly targeting the family of Q subtype potassium channels. It enhances the transmembrane potassium currents, regulating neuronal excitability. This action stabilizes the resting membrane potential, a pivotal factor in mitigating the hyperexcitability that characterizes epilepsy.
Ezogabine has gained approval as an adjunctive treatment...
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Antiepileptic Drugs: Modulators of Neurotransmitter Release Mediated by SV2A Protein

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SV2A is a transmembrane glycoprotein located predominantly in the brain, modulating the release of neurotransmitters for neuronal communication. Both levetiracetam and brivaracetam exhibit a high affinity for...
Effect of Hepatic Disease on Pharmacokinetics: Dose Adjustments Due to Hepatic Impairment01:08

Effect of Hepatic Disease on Pharmacokinetics: Dose Adjustments Due to Hepatic Impairment

Hepatic impairment, characterized by decreased liver function, does not uniformly mandate adjustments in drug dosage. Whether dosage modifications are necessary depends on various factors related to the drug's metabolism and elimination pathways. If a drug is primarily excreted via the kidneys and bypasses significant hepatic processing, if it undergoes minimal metabolic transformation in the liver, or if it is volatile and primarily expelled through the lungs, dose adjustments may not be...
Therapeutic Drug Monitoring: Affecting Factors01:29

Therapeutic Drug Monitoring: Affecting Factors

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Determination of Multiple Dosing Parameters: Steady-State, Minimum and Maximum Concentrations01:15

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Pharmacokinetics: Drug–Drug Interactions

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Related Experiment Videos

Decrease in serum valproic acid levels during treatment with ertapenem.

Fen-Fen Liao1, Yaw-Bin Huang, Chi-Yu Chen

  • 1Department of Pharmacy,Kaohsiung Medical University Hospital, No. 100 Tzyou 1st Road, Kaohsiung, Taiwan. fefeli@cc.kmu.edu.tw

American Journal of Health-System Pharmacy : AJHP : Official Journal of the American Society of Health-System Pharmacists
|July 24, 2010
PubMed
Summary

This study reports a potential drug interaction between valproic acid and ertapenem, leading to significantly reduced valproic acid levels in two patients. Discontinuation of ertapenem therapy resulted in the normalization of valproic acid serum concentrations.

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Area of Science:

  • Pharmacology
  • Clinical Pharmacy
  • Neuroscience

Background:

  • Valproic acid is a widely used antiepileptic drug.
  • Ertapenem is a carbapenem antibiotic.
  • Monitoring drug levels is crucial for effective treatment and patient safety.

Observation:

  • Two patients receiving valproic acid experienced a significant decrease in serum valproic acid levels after the initiation of ertapenem therapy.
  • In both cases, valproic acid levels dropped to below detectable limits (<1 mg/L).

Findings:

  • The reduction in valproic acid levels coincided with ertapenem administration.
  • Following the discontinuation of ertapenem, serum valproic acid levels gradually increased in both patients.
  • No recurrence of seizures was noted despite the initial low valproic acid levels.

Implications:

  • This suggests a potential pharmacokinetic interaction between valproic acid and ertapenem, possibly involving altered drug metabolism or elimination.
  • Clinicians should consider monitoring valproic acid levels when co-administered with ertapenem.
  • Further research is warranted to elucidate the mechanism of this interaction and its clinical significance.