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. 2019 Nov 20;59(8):1916–1926. doi: 10.1093/rheumatology/kez535

Table 3.

Dosage for individual drugs for patients receiving a bDMARD

 Drug Dosage
Standard Under Over Total
Etanercept (originator) 1310 (94.4) 71 (5.1) 7 (0.5) 1388
Etanercept (SB4, biosimilar) 457 (98.5) 7 (1.5) 0 (0) 464
Etanercept (GP2015, biosimilar) 102 (98.1) 2 (1.9) 0 (0) 104
Infliximab (originator) 107 (78.1) 6 (4.4) 24 (17.5) 137
Adalimumab (originator) 1259 (98.9) 5 (0.4) 9 (0.7) 1273
Certolizumab (originator) 710 (94.8) 9 (1.2) 30 (4.0) 749
Golimumab (originator) 362 (97.3) 5 (1.3) 5 (1.3) 372
Abatacept s.c. (originator) 292 (99.3) 2 (0.7) 0 (0) 294
Abatacept i.v. (originator) 150 (81.5) 30 (16.3) 4 (2.2) 185
Rituximab (originator) 581 (90.2) 63 (9.8) 0 (0) 644
Tocilizumab s.c. (originator) 326 (94.8) 8 (2.3) 10 (2.9) 344
Tocilizumab i.v. (originator) 682 (90.8) 36 (4.8) 33 (4.4) 751
Total 6338 (94.5) 245 (3.7) 122 (1.8) 6705

Data are presented as n (%). The available dosage information during the first 3 months of treatment for the drugs shown represents 6705 of 7200 patients receiving a biologic DMARD, i.e. 93.1% of those patients. In case of missing data, the dosage intended at baseline is considered. For tocilizumab and abatacept, s.c. and i.v. routes of administration are shown separately. One abatacept patient was not considered in this table due to an unknown route of administration.