An ulcerated mouth lesion following one dose of sublingual asenapine

G. Sweet, Nicole B Washington, Nancy Brahm
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引用次数: 2

Abstract

Abstract Purpose: To report the first descriptive case of a mouth lesion following one dose of sublingually administered asenapine. Summary: Asenapine is a second-generation antipsychotic, approved in the United States in August 2009, for the treatment of schizophrenia and acute mania associated with bipolar disorder. It is administered as a sublingual tablet to be taken twice daily. Although the mechanism of action has not been fully elucidated, it is thought to be mediated through a combination of antagonist activity at the dopamine and serotonin 5-HT2A receptors. Sublingual bioavailability is estimated at 35% and is highly plasma protein bound (95%). Oral administration results in low bioavailability (< 2%) due to extensive first-pass metabolism. Adverse tissue reactions identified by the manufacturer include mouth ulcers, blisters, and peeling/sloughing of the contact area. In one manufacturer-sponsored trial, oral paresthesia events were reported for the following administration routes: sublingual (7...
一剂舌下阿塞那平后口腔溃疡
摘要目的:报告第一例舌下给药阿塞那平后口腔病变的描述性病例。摘要:阿塞那平是第二代抗精神病药物,于2009年8月在美国获得批准,用于治疗精神分裂症和双相情感障碍相关的急性躁狂症。本品为舌下片剂,每日服用两次。虽然作用机制尚未完全阐明,但它被认为是通过多巴胺和5-羟色胺5-HT2A受体拮抗剂活性的组合介导的。舌下生物利用度估计为35%,与血浆蛋白高度结合(95%)。口服给药导致低生物利用度(< 2%),由于广泛的首过代谢。制造商确定的不良组织反应包括口腔溃疡、水泡和接触区域的脱皮/脱落。在一项制造商赞助的试验中,报告了以下给药途径的口服感觉异常事件:舌下(7…
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