Age-related trends in injection site reaction incidence induced by the tumor necrosis factor-α (TNF-α) inhibitors etanercept and adalimumab: the Food and Drug Administration adverse event reporting system, 2004–2015
Abstract
Tumor necrosis factor-α (TNF-α) inhibitors are increasingly being used as treatment for
rheumatoid arthritis (RA). However, the administration of these drugs carries the risk of inducing
injection site reaction (ISR). ISR gives rise to patient stress, nervousness, and a decrease in quality
of life (QoL). In order to alleviate pain and other symptoms, early countermeasures must be taken
against this adverse event. In order to improve understanding of the risk factors contributing to
the induction of ISR, we evaluated the association between TNF-α inhibitors and ISR by applying a
logistic regression model to age-stratified data obtained from the Food and Drug Administration
Adverse Event Reporting System (FAERS) database.
The FAERS database contains 7,561,254 reports from January 2004 to December 2015. Adjusted
reporting odds ratios (RORs) (95% Confidence Intervals) were obtained for interaction terms for
age-stratified groups treated with etanercept (ETN) and adalimumab (ADA). The adjusted RORs
for ETN* ≥ 70 and ADA* ≥ 70 groups were the lowest among the age-stratified groups undergoing
the respective monotherapies. Furthermore, we found that crude RORs for ETN + methotrexate
(MTX) combination therapy and ADA + MTX combination therapy were lower than those for the
respective monotherapies.
This study was the first to evaluate the relationship between aging and ISR using the FAERS
database.
Keywords:
Etanercept
Adalimumab
Injection Site Reaction
Adverse Event Reporting System
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