Rifampin markedly decreases plasma concentrations of praziquantel in healthy volunteers.

Author: MahatthanatrakulWerawath, PunyoJarurat, RidtitidWibool, SunbhanichMethi, WongnawaMalinee

Paper Details 
Original Abstract of the Article :
Praziquantel is extensively metabolized by the hepatic cytochrome P450 (CYP) enzymes. The CYP3A isoforms are likely to be major enzymes responsible for praziquantel metabolism. Rifampin (INN, rifampicin), a potent enzyme inducer of CYP-mediated metabolism (especially CYP2C9, CYP2C19, and CYP3A4), is...See full text at original site
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引用元:
https://doi.org/10.1067/mcp.2002.129319

データ提供:米国国立医学図書館(NLM)

The Interaction of Rifampin and Praziquantel

This study explores a potential drug interaction between rifampin, an antibiotic, and praziquantel, an antiparasitic drug. The researchers investigated the impact of rifampin on the plasma concentrations of praziquantel in healthy volunteers, finding that rifampin significantly decreases praziquantel levels. This interaction is attributed to rifampin's ability to induce enzymes involved in drug metabolism.

Understanding Drug Interactions

This study highlights the importance of understanding potential drug interactions, particularly when multiple medications are prescribed. It underscores the need for careful monitoring and dose adjustments when patients are taking rifampin and praziquantel together to ensure optimal therapeutic outcomes.

The Importance of Consulting your Healthcare Provider

When taking multiple medications, it's always essential to consult your healthcare provider about potential interactions and any necessary adjustments. By staying informed and communicating openly with your doctor, you can ensure that you receive the best possible care.

Dr.Camel's Conclusion

Like two travelers crossing paths in the vast desert, rifampin and praziquantel can interact in ways that may impact their effectiveness. This study reminds us of the importance of careful navigation when managing multiple medications, ensuring safe and efficient treatment.
Date :
  1. Date Completed 2002-12-12
  2. Date Revised 2018-12-11
Further Info :

Pubmed ID

12426514

DOI: Digital Object Identifier

10.1067/mcp.2002.129319

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English

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