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Patanol Ophthalmic Solution 0.1%(Olopatadine 盐酸奥洛他定滴眼液)
药店国别  
产地国家 日本 
处 方 药: 是 
所属类别 5毫升×10瓶/盒 
包装规格 5毫升×10瓶/盒 
计价单位: 盒 
生产厂家中文参考译名:
协和发酵麒麟公司
生产厂家英文名:
Kyowa Hakko Kirin Co.Ltd.
该药品相关信息网址1:
http://www.info.pmda.go.jp/go/pack/1319752Q1024_2_01/
该药品相关信息网址2:
该药品相关信息网址3:
原产地英文商品名:
Patanol(パタノール点眼液0.1%)5mL×10
原产地英文药品名:
olopatadine hydrochloride
中文参考商品译名:
Patanol(パタノール点眼液0.1%)5毫升×10瓶/盒
中文参考药品译名:
盐酸奥洛他定
曾用名:
简介:

 

部份中文盐酸奥洛他定处方资料(仅供参考)
通用名称:盐酸奥洛他定滴眼液
英文名称:Olopatadine Hydrochloride
商标名称:Patanol Ophthalmic Solution 0.1%
适应症:
用于治疗过敏性结膜炎的体征和症状。
用法用量:
推荐剂量为患眼每次1-2滴,每日2次,间隔6-8小时以上。
不良反应:
已有报告,用药后头痛的发生率为7%。下列不良反应已有报告,发生率小于5% :乏力,视力模糊,烧灼或刺痛感,感冒综合征,眼干,异物感,充血,过敏,角膜炎,眼睑水肿,恶心,咽炎,瘙痒,鼻炎,鼻窦炎及味觉倒错。相当一部分的不良反应和疾病本身的症状相似。
禁忌症:
对任何成份过敏者禁用。
日本协和发酵公司研发。日本爱尔康(Alcon)公司从协和公司引入并将其开发成0.1%滴眼液。上市情况:Allelock于2001年3月在日本上市。Patanol(眼药水)1996年12月获FDA批准,已在30多个国家上市。
日本上市资料附件:http://www.info.pmda.go.jp/go/pack/1319752Q1024_2_01/
Purpose: To compare the clinical efficacy of Patanol® (olopatadine hydrochloride ophthalmic solution 0.1%) to Claritin® (loratadine 10 mg) tablets, in the conjunctival allergen challenge model.
Methods: This was a randomized, double‐masked, single center, contralateral controlled, antigen challenge model study. The concentration of allergen that elicited a positive response was determined at Visits 1 and 2 (itching ≥2 and redness ≥2 OU). At Visit 3, 29 subjects were randomized into two groups. Fifteen subjects received Claritin® tablet and Patanol® ophthalmic solution 0.1% in one eye and placebo in the contralateral eye. Fourteen subjects received placebo tablet and Patanol® in one eye and placebo in the contralateral eye. One hour after drug administration, subjects were challenged with the antigen that elicited a positive response. At 3, 7, and 10 minutes, itching was subjectively eva luated. At Visit 4, the same procedure was followed as in Visit 3, but antigen challenge occurred 8 hours after drug instillation.
Results: Results were analyzed by eye. Eyes treated with Patanol® (concomitant with placebo tablet) had significantly lower ocular itching scores when compared to eyes treated with placebo (concomitant with Claritin®) at 3, 7 and 10 minutes in the onset of action eva luation (p<0.05). Eyes treated with Patanol® (concomitant with placebo tablet) had significantly lower ocular itching scores at 7 minutes and there was a statistical trend (0.05<p<0.1) at 10 minutes in duration of action eva luation.
Conclusions: Patanol® therapy was significantly more efficacious than Claritin® in reducing ocular itching related to allergic conjunctivitis. 

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