Abdullah Abdelaziz, Charles E. Gaber, Preeti Gupta, Todd A. Lee
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引用次数: 0
Abstract
Background
Roflumilast is an add-on therapy for COPD following exacerbations, but real-world safety data in the United States are limited.
Objective
This study aimed to identify safety signals associated with roflumilast initiation through a high-throughput signal detection algorithm.
Methods
Using sequence symmetry analysis (SSA), we analysed Marketscan databases for new roflumilast users (2011–2021). We screened for adverse effects across 211 therapeutic classes within 365 days of initiation. Sensitivity analyses were conducted by sex, age and observation period. Crude and adjusted sequence ratios (cSR and aSR) were reported with 95% confidence intervals (CIs).
Results
Among 11 091 patients (53% aged 65+, 52% female), 32 safety signals were identified. Strong associations were observed with antithyroid agents (aSR, 4.18; 95% CI: 1.66–11.95), parathyroid hormones (aSR, 3.09; 95% CI: 1.56–6.44), haematopoietic agents (aSR, 2.55; 95% CI: 1.07–6.49) and meglitinides (aSR, 2.37; 95% CI: 1.15–5.35). While many signals aligned with prior clinical trial data, novel associations with antithyroid and parathyroid agents were discovered.
Conclusion
In our study, we detected 32 safety signals for roflumilast, including notable associations with antithyroid agents and parathyroid hormones. Future investigations using more robust study designs are warranted to evaluate those signals.
期刊介绍:
Basic & Clinical Pharmacology and Toxicology is an independent journal, publishing original scientific research in all fields of toxicology, basic and clinical pharmacology. This includes experimental animal pharmacology and toxicology and molecular (-genetic), biochemical and cellular pharmacology and toxicology. It also includes all aspects of clinical pharmacology: pharmacokinetics, pharmacodynamics, therapeutic drug monitoring, drug/drug interactions, pharmacogenetics/-genomics, pharmacoepidemiology, pharmacovigilance, pharmacoeconomics, randomized controlled clinical trials and rational pharmacotherapy. For all compounds used in the studies, the chemical constitution and composition should be known, also for natural compounds.