| ADA | Adalimumab |
| AS | Ankylosing spondylitis |
| CD | Crohn’s disease |
| COPD | Chronic obstructive pulmonary disease |
| CTZ | Certolizumab |
| DMARD | Disease-modifying anti-rheumatic drug(s) |
| ETN | Etanercept |
| FAERS | [United States] Food and Drug Administration Adverse Events Reporting System |
| FDA | [United States] Food and Drug Administration |
| GBM | Glioblastoma multiforme |
| GLM | Golimumab |
| HL | Hodgkin’s Lymphoma(s) |
| HR | Hazard ratio(s) |
| HS | Hidradenitis suppurativa |
| INX | Infliximab |
| IQR | Interquartile range |
| IRB | Institutional Review Board |
| JIA | Juvenile idiopathic arthritis |
| MeSH | [National Library of Medicine] Medical subject heading(s) |
| MTX | Methotrexate |
| NHL | Non-Hodgkin’s Lymphoma(s) |
| NMSC | Non-melanoma skin cancer(s) |
| OA | Osteoarthritis |
| PS | Psoriasis |
| PSA | Psoriatic arthritis |
| RA | Rheumatoid arthritis |
| RR | Rate ratio(s) |
| SCC | Squamous cell carcinoma |
| SD | Standard deviation(s) |
| SPA | Spondyloarthropathy/spondyloarthropathies |
| SS | Sjogren’s syndrome |
| TNF-α | Tumor necrosis factor-alpha |
| TNF-i | Tumor necrosis factor-alpha inhibitor(s) |
| TNF-R | Tumor necrosis factor receptor |
| UC | Ulcerative colitis |
| 95% CI | 95% confidence interval |