↑ Engelhardt, G; Homma, D; Schlegel, K; Utzmann, R; Schnitzler, C (tháng 10 năm 1995). “Anti-inflammatory, analgesic, antipyretic and related properties of meloxicam, a new non-steroidal anti-inflammatory agent with favourable gastrointestinal tolerance”. Inflammation Research 44 (10): 423–433. PMID8564518. doi:10.1007/BF01757699. Chú thích sử dụng tham số |month= bị phản đối (trợ giúp)
1 2 Hawkey, C; Kahan, A; Steinbrü, K; Alegre, C; Baumelou, E; Bégaud, B; Dequeker, J; Isomäki, H; Littlejohn, G (tháng 9 năm 1998). “Gastrointestinal tolerability of meloxicam compared to diclofenac in osteoarthritis patients”. Rheumatology 37 (9): 937–945(9). doi:10.1093/rheumatology/37.9.937. Chú thích sử dụng tham số |month= bị phản đối (trợ giúp)
↑ Dequeker, J; Hawkey, C; Kahan, A; Steinbruck, K; Alegre, C; Baumelou, E; Begaud, B; Isomaki, H; Littlejohn, G (1998). “Improvement in gastrointestinal tolerability of the selective cyclooxygenase (COX)-2 inhibitor, meloxicam, compared with piroxicam: results of the Safety and Efficacy Large-scale Evaluation of COX- inhibiting Therapies (SELECT) trial in osteoarthritis”. The British Journal of Rheumatology 37 (9): 946–51. PMID9783758. doi:10.1093/rheumatology/37.9.946.
↑ Wojtulewski, JA; Schattenkirchner, M; Barceló, P; Le Loët, X; Bevis, PJR; Bluhmki, E; Distel, M. “A Six-Month Double-Blind Trial to Compare the Efficacy and Safety of Meloxicam 7.5 mg Daily and Naproxen 750 mg Daily in Patients with Rheumatoid Arthritis”. Rheumatology. 35, Supplement 1: 22–8.
