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. 2016 Sep;22(9):10.18553/jmcp.2016.22.9.1088. doi: 10.18553/jmcp.2016.22.9.1088

TABLE 4.

Adverse Drug Eventsa

Product Major ADR (%) Minor ADR (%) Placebo-Adjusted Minor ADR (%)
Tofacitinib 1.50 4.50 4.50
Adalimumab 2.49 17.00 4.32
Etanercept 2.01 13.00 4.18
Certolizumab 3.72 6.00 9.90
Tocilizumab 2.69 6.00 3.30
Rituximab 1.84 2.00 3.77
Abatacept 1.51 5.00 4.40

Sources: Major ADRs: Strand V, Ahadieh S, French J, et al. Systematic review and meta-analysis of serious infections with tofacitinib and biologic disease-modifying anti-rheumatic drug treatment in rheumatoid arthritis clinical trials.36 Minor ADRs: U.S. prescribing information for each product.13,22,37-41

aRate of adverse drug events are presented at 6 months for each therapy option. ADR = adverse drug reaction.

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