Affiliations 

  • 1 Department of Pharmacy, University of Rajshahi, Rajshahi, 6205, Bangladesh. biswas_07pharm@ru.ac.bd
  • 2 Department of Pharmacy, University of Rajshahi, Rajshahi, 6205, Bangladesh
  • 3 Department of Medicine, Faridpur Medical College Hospital, Faridpur, Bangladesh
  • 4 School of Pharmaceutical Sciences, Universiti Sains Malaysia, Penang, Malaysia
Int J Clin Pharm, 2021 Oct;43(5):1360-1369.
PMID: 33774763 DOI: 10.1007/s11096-021-01261-y

Abstract

Background Efficacy of clopidogrel may be diminished due to either co-administration of proton pump inhibitors or carrying CYP2C19 loss-of-function alleles. However, patients may be at greater risk of major adverse cardiovascular events if taking clopidogrel together with proton pump inhibitors and also inherited the CYP2C19 loss-of-function alleles which may cause further reduction of clopidogrel efficacy. This is due to the cumulative effects of drug-drug interactions and drug-gene interactions collectively referred to as multifactorial drug-gene interactions. Aim of the review The aim of this analysis was to estimate aggregated risk of major adverse cardiovascular events for either coronary heart disease or stroke patients with multifactorial drug-gene interactions versus clopidogrel alone with or without drug-gene interactions. Methods Literatures were searched using different resources based on the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. Meta-analysis was performed using RevMan software following either fixed/random effects model based on the levels of heterogeneity. A p value 

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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