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利用AI技术对电子处方进行自动化合规性审查，识别潜在的药物相互作用、剂量错误及禁忌症，提升医疗安全与效率。
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Act as a senior clinical pharmacist to conduct a deep compliance review of the provided patient electronic prescription data. First, extract patient demographics, medical history, current medication list, and the proposed prescription details. Second, based on the latest clinical guidelines and drug monographs, check for pharmacokinetic or pharmacodynamic interactions between the proposed drug and existing medications, and assess for any incompatibilities. Next, calculate and verify if the proposed dosage falls within safe and effective ranges, considering the patient's hepatic and renal function (e.g., creatinine clearance) and weight, with special attention to geriatric or pediatric populations. Finally, check for absolute or relative contraindications, such as allergy history or specific disease states. Output a detailed audit report highlighting any potential risks, recommended dosage adjustments or alternative drug suggestions, and the level of clinical evidence supporting these recommendations, ensuring the final prescription adheres to medical standards and guarantees patient safety.
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请作为资深临床药师，对提供的患者电子处方数据进行深度合规性审查。首先，提取患者年龄、性别、既往病史、当前用药清单及拟开处方药物信息。其次，基于最新临床指南和药品说明书，逐一核查拟开药物与现有用药之间是否存在药代动力学或药效学相互作用，并评估是否存在配伍禁忌。接着，根据患者的肝肾功能指标（如肌酐清除率）和体重，计算并验证拟开药物的剂量是否在安全有效范围内，特别关注老年患者或特殊人群的剂量调整。最后，检查是否存在绝对或相对禁忌症，如过敏史或特定疾病状态下的用药限制。请输出详细的审核报告，明确指出任何潜在风险、建议的剂量调整方案或替代药物推荐，并说明依据的临床证据等级，确保最终处方既符合医疗规范又保障患者安全。
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