Safety of triazole antifungals: a pharmacovigilance study from 2004 to 2021 based on FAERS

Shuang Chai1,2, Jing-Lun Zhan1,2, Li-Mei Zhao1,2

  • 1Department of Pharmacy, Shengjing Hospital of China Medical University, Shenyang, China.

Abstract

Insights

Triazole antifungals can cause serious adverse events (AEs) affecting endocrine, metabolic, and skin systems. This study identified more AEs than listed in drug information, highlighting the need for careful monitoring during treatment.

Area of Science:

  • Pharmacovigilance
  • Clinical Pharmacology
  • Drug Safety

Background:

  • Triazole antifungals are broad-spectrum agents used to treat fungal infections.
  • Numerous undetected and unreported adverse events (AEs) associated with triazole antifungals exist.
  • Understanding these AEs is crucial for patient safety.

Purpose of the Study:

  • To assess the association between triazole antifungals and adverse events (AEs) and important medical events (IMEs).
  • To identify specific system organ classes (SOCs) and AEs linked to triazole antifungal use.
  • To provide updated safety information for clinicians.

Main Methods:

  • Disproportionality analysis of data from the Food and Drug Administration Adverse Event Reporting System (FAERS).
  • Inclusion of data from Q1 2004 to Q3 2021.
  • Identification and analysis of triazole antifungal-IME pairs.

Main Results:

  • A total of 22,566 triazole antifungal records were analyzed, with 9584 triazole antifungal-IME pairs.
  • Significant signals were observed in 'Endocrine disorders' (ROR=167.94), 'Metabolism and nutrition disorders' (ROR=46.30), and 'Skin and subcutaneous tissue disorders' (ROR=21.37).
  • Common AEs included respiratory failure, rash, abnormal hepatic function, and hypokalemia; uncommon AEs included QT interval changes, neurotoxicity, pseudoaldosteronism, and hallucinations.

Conclusions:

  • Triazole antifungals are associated with a range of AEs, varying in type and intensity.
  • Findings align with existing literature but suggest additional AEs not fully detailed in prescribing information.
  • Further pharmacoepidemiological studies are recommended to confirm AEs with modest incidence but high signal strength.

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