目的制备咽炎合剂并观察临床疗效。方法建立咽炎合剂的制备方法和质控标准,并对急慢性咽炎176例随机分成治疗组和对照组治疗。结果本合剂制作工艺可行,质量控制可靠,治疗组有效率为97.9%,对照组有效率90%(P<0.05)。结论咽炎合剂配方合理,疗效确切,无明显不良反应。 Objective To prepare pharyngitis mixture and observe the clinical efficacy. Methods The preparation methods and quality control criteria of pharyngitis mixture were established. 176 cases of acute and chronic pharyngitis were randomly divided into treatment group and control group. Results The preparation process of this mixture was feasible and the quality control was reliable. The effective rate was 97.9% in the treatment group and 90% in the control group (P<0.05). Conclusion Pharyngitis mixture formula is reasonable and effective, no obvious adverse reactions.