英文摘要 |
For the evaluation of acute pain relief in rheumatic conditions, parenteral form of tenoxicam, including intravenous (IV) and intramuscular (IM) forms were used to assess the clinical therapeutic effect. A total of 30 rheumatic patients enrolled into this study. Patients were classified into 2 groups, 15 patients receiving IV form and another 15 receiving IM form. After consecutive 3 days IV or IM tenoxicam treatment, the results showed good efficacy in both groups. The onset of joint pain relief was at 1 hour after tenoxicam injection and the maximal effect of joint pain relief reached at 3 hours later. The adverse effects of tenoxicam injection were mild and only 10 percent of patients experienced. Meanwhile, there were also no one to discontinue the drug for their adverse effects. In conclusion, tenoxicam 20 mg IV and IM can therefore be safely prescribed for the effective treatment of acute pain in rheuamtic conditions. |