van Ahlen H, Zumbé J, Stauch K, Landen H
Klinikum Osnabruck, Osnabruck, Germany.
J Int Med Res. 2005 May-Jun;33(3):337-48. doi: 10.1177/147323000503300309.
We assessed the safety, efficacy and patient acceptability of vardenafil (Levitra, Bayer HealthCare, Leverkusen, Germany) under real-life conditions in patients with erectile dysfunction (ED) in a multinational post-marketing surveillance study. An initial and up to two follow-up visits were documented for 29 358 German ED patients receiving vardenafil. Patients were interviewed about overall treatment success, and individual sexual attempts were evaluated in a patient questionnaire. Overall erectile improvement was reported by 93.9% of physicians, and similar improvement rates were reported for both 10 mg and 20 mg vardenafil dosages. Most patients experienced improved erections after the first (73.6%) or second (88.5%) tablet. Sexual attempts were successful with respect to partner penetration in 94.9% of patients and with respect to maintenance of erection during intercourse in 87.7% of patients. Adverse drug reactions were very rare (1.3% of patients). Vardenafil was highly effective, reliable and well tolerated in ED patients treated under real-life conditions.
在一项跨国上市后监测研究中,我们评估了伐地那非(艾力达,拜耳医疗保健公司,德国勒沃库森)在现实生活条件下对勃起功能障碍(ED)患者的安全性、有效性和患者可接受性。记录了29358名接受伐地那非治疗的德国ED患者的首次就诊情况以及最多两次随访情况。就总体治疗成功情况对患者进行了访谈,并通过患者问卷对个体性尝试进行了评估。93.9%的医生报告总体勃起功能有改善,10毫克和20毫克伐地那非剂量的改善率相似。大多数患者在服用第一片(73.6%)或第二片(88.5%)后勃起功能得到改善。94.9%的患者在与性伴侣性交时成功插入,87.7%的患者在性交过程中能够维持勃起。药物不良反应非常罕见(占患者的1.3%)。在现实生活条件下接受治疗的ED患者中,伐地那非高效、可靠且耐受性良好。