Mikó Péter
Novartis Hungária Kft. Consumer Health, Budapest.
Orv Hetil. 2004 Feb 15;145(7):327-9.
Dimethindene maleate, the active substance of the extended-release Fenistil 24 capsule, is a first-generation histamine receptor antagonist, which is marketed in 10 European countries. In Hungary approximately 200,000 boxes are sold yearly from this product, which is mainly used for treatment of symptoms associated with allergic diseases (urticaria, itch, hay fever) The aim of the present study was to gather information with the help of medical doctors about the indications, efficacy and primarily the safety of use, observed side effects and frequency of adverse events associated with this product.
During the study 4574 questionnaires were evaluated out of the 5578 filled by 249 doctors. Responses were included into the evaluation only if the address and type of polyclinic of the doctor filling the questionnaire, indication of the use of the product could be precisely identified and the patient returned for control visit at least once.
Based on the study results in Hungary in most cases the product is prescribed according to the indications and dosing schedule given in the SPC. In this study participating doctors found the drug to be effective in 95% of cases. Unexpected, new adverse events were not observed during the study. Approximately 22% of patients reported adverse events, tiredness and sleepiness being the most frequent ones. Occurrence of sedative adverse events was more frequent among those who were prone to tiredness (51 vs. 17%). The adverse events most frequently were reported 10-12 hours after intake. The average length of treatment was 4 weeks or less. The medicine is taken usually at night, before going to sleep.
In Hungary in most cases the product is prescribed according to the indications and dosing schedule given in the current approved Summary of Product Characteristics.
马来酸氯苯那敏,即缓释非尼斯特24胶囊的活性成分,是第一代组胺受体拮抗剂,在10个欧洲国家上市。在匈牙利,该产品每年销量约为20万盒,主要用于治疗与过敏性疾病相关的症状(荨麻疹、瘙痒、花粉症)。本研究的目的是借助医生收集有关该产品的适应症、疗效,主要是使用安全性、观察到的副作用以及不良事件发生频率的信息。
在研究过程中,对249名医生填写的5578份问卷中的4574份进行了评估。只有当填写问卷的医生的诊所地址和类型、产品使用适应症能够精确确定,且患者至少返回进行一次复查时,其回复才被纳入评估。
根据匈牙利的研究结果,在大多数情况下,该产品是按照产品特性总结(SPC)中给出的适应症和给药方案开具的。在本研究中,参与的医生发现该药物在95%的病例中有效。在研究期间未观察到意外的新不良事件。约22%的患者报告了不良事件,疲劳和嗜睡是最常见的。在容易疲劳的人群中,镇静性不良事件的发生率更高(51%对17%)。不良事件大多在服药后10 - 12小时报告。平均治疗时长为4周或更短。该药物通常在晚上睡觉前服用。
在匈牙利,大多数情况下该产品是按照当前批准的产品特性总结中给出的适应症和给药方案开具的。