Literature DB >> 29187701

Association between Concomitant Use of Acyclovir or Valacyclovir with NSAIDs and an Increased Risk of Acute Kidney Injury: Data Mining of FDA Adverse Event Reporting System.

Zhihua Yue1, Jinhai Shi2, Haona Li3, Huiyi Li1.   

Abstract

Nonsteroidal anti-inflammatory drugs (NSAIDs) are likely to be used concomitantly with acyclovir or valacyclovir in clinical practice, but the study on the safety of such combinations was seldom reported. The objective of the study was to investigate reports of acute kidney injury (AKI) events associated with the concomitant use of oral acyclovir or valacyclovir with an NSAID by using the United States Food and Drug Administration (FDA) Adverse Event Reporting System (AERS) database between January 2004 and June 2012. The frequency of AKI events in patients while simultaneously taking either acyclovir or valacyclovir and an NSAID was compared using the Chi-square test. The effect of concomitant use of acyclovir or valacyclovir and individual NSAIDs on AKI was analyzed by the reporting odds ratio (ROR). The results showed that AKI was reported as the adverse event in 8.6% of the 10923 patients taking valacyclovir compared with 8.7% of the 2556 patients taking acyclovir (p=NS). However, AKI was significantly more frequently reported in patients simultaneously taking valacyclovir and an NSAID (19.4%) than in patients simultaneously taking acyclovir and an NSAID (10.5%) (p<0.01). The results also suggested that increased risk of AKI was likely associated with the concomitant use of valacyclovir and some NSAIDs such as loxoprofen, diclofenac, etodolac, ketorolac, piroxicam or lornoxicam. The case series from the AERS indicated that compared with acyclovir, valacyclovir is more likely to be affected by NSAIDs, and the concomitant use of valacyclovir with some NSAIDs might be associated with increased risk of AKI. The drug interactions with this specific combination of medications are worth exploring further.

Entities:  

Keywords:  FDA Adverse Event Reporting System (FAERS); acute kidney injury; acyclovir; data mining; nonsteroidal anti-inflammatory drug (NSAID); valacyclovir

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Substances:

Year:  2017        PMID: 29187701     DOI: 10.1248/bpb.b17-00547

Source DB:  PubMed          Journal:  Biol Pharm Bull        ISSN: 0918-6158            Impact factor:   2.233


  3 in total

1.  Analyzing adverse drug reaction using statistical and machine learning methods: A systematic review.

Authors:  Hae Reong Kim; MinDong Sung; Ji Ae Park; Kyeongseob Jeong; Ho Heon Kim; Suehyun Lee; Yu Rang Park
Journal:  Medicine (Baltimore)       Date:  2022-06-24       Impact factor: 1.817

2.  Risk Evaluation for Acute Kidney Injury Induced by the Concomitant Use of Valacyclovir, Analgesics, and Renin-Angiotensin System Inhibitors: The Detection of Signals of Drug-Drug Interactions.

Authors:  Ichiro Inaba; Yuki Kondo; Shinya Iwasaki; Satoko Tsuruhashi; Ayano Akaishi; Kazuya Morita; Kentaro Oniki; Junji Saruwatari; Yoichi Ishitsuka; Tetsumi Irie
Journal:  Front Pharmacol       Date:  2019-08-08       Impact factor: 5.810

3.  Leflunomide increased the renal exposure of acyclovir by inhibiting OAT1/3 and MRP2.

Authors:  Xiao-Ying Liao; Qiang-Qiang Deng; Li Han; Zhi-Tao Wu; Zhao-Liang Peng; Yuan Xie; Guang-Ji Wang; Ji-Ye Aa; Guo-Yu Pan
Journal:  Acta Pharmacol Sin       Date:  2019-07-24       Impact factor: 6.150

  3 in total

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