Zurlo J J, Frank M M
Laboratory of Clinical Investigation, National Institutes of Health, Bethesda, Maryland 20892.
Fertil Steril. 1990 Jul;54(1):64-72. doi: 10.1016/s0015-0282(16)53638-3.
Although the short-term safety (less than or equal to 6 months) of danazol has been established in a variety of settings, no information exists as to its long-term safety. We therefore investigated the long-term safety of danazol by performing a retrospective chart review of 60 female patients with hereditary angioedema treated with danazol for a continuous period of 6 months or longer. The mean age of the patients was 35.2 years and the mean duration of therapy was 59.7 months. Virtually all patients experienced one or more adverse reactions. Menstrual abnormalities (79%), weight gain (60%), muscle cramps/myalgias (40%), and transaminase elevations (40%) were the most common adverse reactions. The drug was discontinued due to adverse reactions in 8 patients. No patient has died or suffered any apparent long-term sequelae that were directly attributable to the drug. We conclude that, despite a relatively high incidence of adverse reactions, danazol has proven to be remarkably safe over the long-term in this group of patients.
尽管达那唑的短期安全性(小于或等于6个月)已在多种情况下得到证实,但关于其长期安全性尚无相关信息。因此,我们通过对60例接受达那唑持续治疗6个月或更长时间的遗传性血管性水肿女性患者进行回顾性病历审查,来研究达那唑的长期安全性。患者的平均年龄为35.2岁,平均治疗时长为59.7个月。几乎所有患者都经历了一种或多种不良反应。月经异常(79%)、体重增加(60%)、肌肉痉挛/肌痛(40%)和转氨酶升高(40%)是最常见的不良反应。8例患者因不良反应停药。没有患者死亡或出现任何明显的直接归因于该药物的长期后遗症。我们得出结论,尽管不良反应发生率相对较高,但在这组患者中,达那唑长期以来已被证明是相当安全的。