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Pharmacovigilance of triazole antifungal agents: Analysis of the FDA adverse event reporting system (FAERS) database
Jianxing Zhou1,2, Zipeng Wei1,2, Baohua Xu1,2
1Department of Pharmacy, Fujian Medical University Union Hospital, Fuzhou, Fujian, China.
Abstract:
Triazole antifungal drugs (TAD) are widely used to treat invasive fungal infections due to their broad antifungal spectrum and low toxicity. Despite their preference in the clinic, multiple Adverse Events (AE) are still reported each year.
Objective:
We aimed to characterize the distribution of Adverse Events associated with Triazole antifungal drugs in different systems and to identify Important Medical Events (IME) signals for Triazole antifungal drugs.
Methods:
The U.S. Food and Drug Administration Adverse Event Reporting System (FAERS) was queried for Adverse Events related to Triazole antifungal drugs from 2012 to 2022. The Adverse Events caused by all other drugs and non-TAD antifungal drugs were analyzed as references. Reporting odds ratio and Bayesian confidence propagation neural network of information components were used to evaluate the association between Triazole antifungal drugs and Important Medical Events. Visual signal spectrum is mapped to identify potential adverse reaction signals.
Results:
Overall, 10,262 Adverse Events were reported to be associated with Triazole antifungal drugs, of which 5,563 cases were defined as Important Medical Events. Common adverse drug reactions (ADR) mentioned in the instructions such as delirium and hypokalemia were detected, as well as unlabeled ADRs such as rhabdomyolysis and hepatitis fulminant. Cholestasis, drug-induced liver injury, QT interval prolongation and renal impairment have notable signals in all Triazole antifungal drugs, with 50 percent of patients developing a severe clinical outcome. Isavuconazole had the lowest signal intensity and demonstrated a superior safety profile.
Conclusion:
Most results are generally consistent with previous studies and are documented in the prescribing instructions, but some IMEs are not included, such as hepatitis fulminant. Additional pharmaco-epidemiological or experimental studies are required to validate the small number of unlabeled ADRs. TAD-related Important Medical Eventshave a considerable potential to cause clinically serious outcomes. Clinical use of Triazole antifungal drugs requires more attention.
Insights
Triazole antifungal drugs (TAD) can cause serious adverse events, including unlabeled reactions like rhabdomyolysis. While generally consistent with known side effects, some important medical events require further study to ensure patient safety.
Area of Science:
- Pharmacovigilance
- Drug Safety
- Mycology
Background:
- Triazole antifungal drugs (TAD) are crucial for treating invasive fungal infections due to their efficacy and low toxicity.
- Despite clinical preference, TAD are associated with numerous reported Adverse Events (AE) annually.
Purpose of the Study:
- To analyze the distribution of TAD-related Adverse Events across different organ systems.
- To identify signals for Important Medical Events (IME) associated with TAD use.
Main Methods:
- Utilized the U.S. FDA Adverse Event Reporting System (FAERS) data from 2012-2022.
- Employed statistical methods like reporting odds ratio and Bayesian neural networks to detect IME signals.
- Mapped visual signal spectrum to identify potential adverse reaction signals.
Main Results:
- Identified 10,262 TAD-related Adverse Events, with 5,563 classified as Important Medical Events.
- Confirmed known side effects (e.g., delirium, hypokalemia) and detected unlabeled ADRs (e.g., rhabdomyolysis, fulminant hepatitis).
- Notable IME signals included cholestasis, drug-induced liver injury, QT prolongation, and renal impairment, with 50% of patients experiencing severe outcomes; isavuconazole showed the best safety profile.
Conclusions:
- Findings align with existing literature but highlight previously undocumented IMEs like fulminant hepatitis.
- Further research is needed to validate unlabeled ADRs.
- TAD-related IMEs pose significant risks for severe clinical outcomes, necessitating increased clinical vigilance.
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