Table 2.
Characteristics of oral methotrexate prior to subcutaneous methotrexate treatment and subcutaneous methotrexate utilization in UMAR study
| Characteristics | Missing (n) | |
|---|---|---|
| Oral methotrexate | ||
| Duration, months (mean ± SD) | 55.84 ± 53.32 | 3 |
| Mean dose (mean ± SD) | 14.31 ± 0.46 | |
| Reason for treatment discontinuation [n (%)] | 4 | |
| Adverse events | 13 (28.26) | |
| Lack of efficacy | 32 (69.57) | |
| Adverse events and other | 1 (2.17) | |
| Subcutaneous methotrexate | ||
| Mean dose, mg (mean ± SD) | 18.36 ± 0.53 | |
| Dose, mg [n (%)]; mean duration (months) | ||
| 8 | 1 (2.00); 3.68 | |
| 10 | 11 (22.00); 14.72 | |
| 15 | 24 (48.00); 17.02 | |
| 20 | 31 (62.00); 15.63 | |
| 25 | 12 (24.00); 24.08 | |
| Reason for treatment discontinuation [n (%)] | ||
| Adverse events | 6 (66.67) | |
| Lack of efficacy | 2 (22.22) | |
| Other | 1 (11.11) | |
The sum differs (9 = 100%) since one participant discontinued the treatment due to more than one reason
SD standard deviation, UMAR Utilization of Metoject® in Rheumatoid Arthritis