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. 2023 Feb 24;62(10):3400–3408. doi: 10.1093/rheumatology/kead074

Table 3.

Reasons for discontinuation of baricitinib in the BSRBR-RA

Reason for discontinuation n %
6-month follow-up
Lack of efficacy 14 24.6
Adverse events 36 63.2
Other 7 12.3
12-month follow-up
Lack of efficacy 8 25.0
Adverse events 20 62.5
Other 4 12.5

A total of 59 patients with at least one recorded follow-up discontinued baricitinib by the 6-month follow-up and 34 patients with at least one recorded follow-up discontinued baricitinib by the 12-month follow-up; two patients had missing data at the 6-month follow-up and two patients had missing data at the 6-month follow-up.

n: number of patients with reported reason.