2. Summary of outcomes: adverse events and withdrawals.
Adverse events | Withdrawals | ||||
Study ID | Treatment | Any | Serious | Adverse event | Other |
Moller 2008 | (1) Lornoxicam 8 mg SR, n = 80 (2) Lornoxicam 8 mg QR, n = 80 (3) Placebo, n = 40 |
at 7 days: (1) 39/80 (2) 43/80 (3) 14/40 |
None | None | None |
Norholt 1995 | (1) Lornoxicam 4 mg, n = 43 (2) Lornoxicam 8 mg, n = 45 (3) Lornoxicam 16 mg, n = 48 (4) Lornoxicam 32 mg, n = 48 (5) Ketorolac 10 mg, n = 46 (6) Placebo, n = 48 |
No usable data | None reported | None | None |
Patel 1991 | (1) Lornoxicam 2 mg, n = 30 (2) Lornoxicam 4 mg, n = 30 (3) Lornoxicam 8 mg, n = 30 (4) Aspirin 650 mg, n = 30 (6) Placebo, n = 30 |
at 8 h: (1) 3/30 (2) 1/30 (3) 2/30 (4) 2/30 (5) 2/30 |
None | None | None |
QR ‐ quick release; SR ‐ slow release