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. 2020 Sep 30;10:16178. doi: 10.1038/s41598-020-73183-0

Table 3.

Patients that stopped bETA for any reason.

PTS Sex Age DGN DIS DUR (yy) oETA (mm) bETA (mm) LoE AE SF Measures taken Outcome after interruption
1 F 68 RA 10 26 4 Swap to a tsDMARD Clinical improvement
2 F 58 RA 21 34 8 Swap to an other bDMARD Partially improvement
3 F 85 RA 22 102 6 Swap to an other bDMARD Clinical improvement
4 M 69 RA 14 92 7 Psoriasis (new onset) Switch back to originator Resolved
5 F 63 RA 16 78 6 Arthralgia worsening Switch back to originator Resolved
6 F 66 PsA 4 26 8 Swich to an other bDMARD; swap to an other bDMARD Coutaneous rash; clinical improvement
7 F 71 PsA 18 186 6 Swich to an other bDMARD Partially improvement
8 F 70 PsA 17 52 7 Swich to an other bDMARD Clinical improvement
9 F 74 PsA 10 89 1 Cutaneous rash Switch back to originator Resolved
10 F 75 PsA 10 45 4 Arthralgia worsening Switch back to originator Resolved
11 M 58 AS 13 84 4 Switch back to originator Resolved

PTS patients, DGN diagnosis, DIS DUR disease duration, LoE lack of efficacy, AE adverse event, SF subjective features, yy years, mm months, bDMARD biologic disease-modifying antirheumatic drug, tsDMARD targeted synthetic disease-modifying antirheumatic drug.