National gonorrhea therapy monitoring study: adverse drug reactions.

H W Jaffe, G H Reynolds, P J Wiesner
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Abstract

The Center for Disease Control and cooperating clinics monitored adverse drug reactions in 6,969 patients who were treated for suspected uncomplicated gonorrhea with one of the four 1972 United States Public Health Service (USPHS) recommended regimens and returned for reexamination. Of those patients receiving the aqueous procaine penicillin G (APPG)-probenecid regimen, 2.0% had at least one adverse reaction and 0.18% experienced procaine reactions. No life-threatening reactions occurred. The overall reaction rates for the ampicillin-probenecid, tetracycline and spectinomycin regimens were 0.62%, 5.9%, and 0.61%, respectively. Our findings document the relative safety of the USPHS recommended regimens.

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全国淋病治疗监测研究:药物不良反应。
疾病控制中心和合作诊所监测了6,969名疑似无并发症淋病患者的药物不良反应,这些患者接受了1972年美国公共卫生局(USPHS)推荐的四种治疗方案之一的治疗,并返回进行重新检查。在接受普鲁卡因青霉素G (APPG)-probenecid方案的患者中,2.0%出现至少一种不良反应,0.18%出现普鲁卡因反应。没有发生危及生命的反应。氨苄青霉素-丙烯酸、四环素和大观霉素方案的总反应率分别为0.62%、5.9%和0.61%。我们的研究结果证明了USPHS推荐方案的相对安全性。
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