Clopidogrel, a CYP2C8 inhibitor, causes a clinically relevant increase in the systemic exposure to the active metabolite of selexipag in healthy subjects.

Author: AxelsenLene Nygaard, BrudererShirin, Perez RuixoJuan Jose, PoggesiItalo, RasschaertFreya

Paper Details 
Original Abstract of the Article :
Selexipag is a prostacyclin receptor agonist approved for the treatment of pulmonary arterial hypertension. Cytochrome P450 (CYP) 2C8 is involved in the metabolism of selexipag and its active metabolite, ACT-333679. This study evaluated the interaction of selexipag and clopidogrel, a CYP2C8 inhibito...See full text at original site
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引用元:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9328278/

データ提供:米国国立医学図書館(NLM)

Drug Interactions: When Medications Collide in the Desert

In the vast world of pharmaceuticals, interactions between drugs are a common concern. This study explores the potential interaction between selexipag, a medication for pulmonary arterial hypertension, and clopidogrel, an anti-platelet drug. Imagine these medications as two different desert caravans, each with its own course and destination. The researchers investigated whether clopidogrel, known to inhibit a specific enzyme involved in selexipag metabolism, could alter selexipag's effects in the body.

Navigating Drug Interactions

The researchers found that clopidogrel indeed affected selexipag metabolism, leading to increased levels of the active selexipag metabolite in the body. This finding underscores the importance of careful consideration of drug interactions, particularly when patients are taking multiple medications.

Staying Informed About Your Medications

Always discuss your medications with your physician or pharmacist to ensure that they are appropriate for your individual needs and that potential interactions are minimized.

Dr.Camel's Conclusion

This study reminds us that even in the vast expanse of the pharmaceutical desert, a careful eye is needed to avoid the potential pitfalls of drug interactions. By understanding these interactions, we can navigate the medicinal landscape with greater safety and effectiveness.

Date :
  1. Date Completed 2021-07-28
  2. Date Revised 2022-07-31
Further Info :

Pubmed ID

32415684

DOI: Digital Object Identifier

PMC9328278

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Languages

English

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