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Treating pain in patients with hepatic impairment

机译:治疗肝功能不全患者的疼痛

摘要

An extended release composition for an analgesic active pharmaceutical ingredient which may be an opioid, preferably hydrocodone as the only active ingredient. The extended release composition preferably comprises a extended release composition which may be in the form of beads contained in an oral dosage form such as gelatin capsules. The composition is designed to release hydrocodone in a way such that the increase in hydrocodone exposure in hepatically impaired patients is not clinically significant. The oral dosage units are supplied as part of a kit, which also includes a primary package and a package insert all sold as a commercially marketed product. The primary package and package insert are contained in an optional secondary package and the package insert does not contain a warning, a dosing instruction, or a dosing table specifically directed to patients suffering from mild, moderate or severe hepatic impairment, and preferably explicitly states that dosing adjustment is not required for mild or moderate hepatic impairment.
机译:用于止痛活性药物成分的缓释组合物,其可以是阿片样物质,优选氢可酮作为唯一的活性成分。缓释组合物优选包含缓释组合物,其可以呈口服剂型如明胶胶囊中所含的珠粒形式。该组合物被设计成以使得肝受损患者中氢可酮暴露的增加在临床上不显着的方式释放氢可酮。口服剂量单位作为试剂盒的一部分提供,该试剂盒还包括主要包装和包装插页,所有包装均作为市售产品出售。主包装和包装插页包含在可选的辅助包装中,且包装插页不包含警告,剂量说明或剂量表,特别针对患有轻度,中度或严重肝功能不全的患者,最好明确声明:对于轻度或中度肝功能损害,无需调整剂量。

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