Efficacy and Safety of Bepotastine Besilate in the Treatment of Chronic Urticaria
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- FURUMURA Minao
- Department of Dermatology, Fukuoka University School of Medicine
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- KUBOTA Yumiko
- Department of Dermatology, Fukuoka University School of Medicine
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- NAKAYAMA Juichiro
- Department of Dermatology, Fukuoka University School of Medicine
Bibliographic Information
- Other Title
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- 慢性蕁麻疹に対するベシル酸ベポタスチン(タリオン<SUP>®</SUP>錠)の臨床的有用性の検討
- 治療 慢性蕁麻疹に対するベシル酸ベポタスチン(タリオン錠)の臨床的有用性の検討
- チリョウ マンセイ ジンマシン ニ タイスル ベシルサン ベポタスチン タリオンジョウ ノ リンショウテキ ユウヨウセイ ノ ケントウ
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Abstract
The efficacy and safety of bepotastine besilate (Talion®) in the treatment of chronic urticaria were evaluated in 88 adult patients with chronic urticaria. Patients were openly treated with 20 mg/day oral bepotastine besilate for 14 days. Clinical evaluations were performed every 7 days, and patients were asked to keep a diary, recording their pruritus scores. Symptoms improved in 77.1% of the patients after two weeks and pruritus scores were reduced significantly within 24 h after oral administration in 69.6% of patients. It appears that bepotastine besilate can be ranked as a drug of first choice for the treatment of chronic urticaria, because it rapidly relieved itch and the incidence of drowsiness was relatively low.
Journal
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- Nishi Nihon Hifuka
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Nishi Nihon Hifuka 68 (1), 69-75, 2006
Western Division of Japanese Dermatological Association
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Keywords
Details 詳細情報について
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- CRID
- 1390282679274714240
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- NII Article ID
- 10018351166
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- NII Book ID
- AN00183881
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- ISSN
- 18804047
- 03869784
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- NDL BIB ID
- 7864963
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- Text Lang
- ja
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- Data Source
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- JaLC
- NDL
- Crossref
- CiNii Articles
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- Abstract License Flag
- Disallowed