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類別 藥政管理類,藥品優良調劑作業準則
法規性質 法規命令
法規名稱 藥品優良調劑作業準則
條文內容 <p><span style="font-family: 新細明體,serif;">第</span><span style="font-family: calibri;">&nbsp;&nbsp; 1&nbsp;&nbsp; </span><span style="font-family: 新細明體,serif;">條</span><span style="font-family: calibri;">&nbsp; </span><span style="font-family: 新細明體,serif;">本準則依藥事法</span><span style="font-family: calibri;"> (</span><span style="font-family: 新細明體,serif;">以下簡稱本法</span><span style="font-family: calibri;">) </span><span style="font-family: 新細明體,serif;">第三十七條第一項規定訂定之。</span> </p><p><span style="font-family: 新細明體,serif;">第</span><span style="font-family: calibri;">&nbsp;&nbsp; 2&nbsp;&nbsp; </span><span style="font-family: 新細明體,serif;">條</span><span style="font-family: calibri;">&nbsp; </span><span style="font-family: 新細明體,serif;">本準則所稱藥事人員,係指依法執業之藥師及藥劑生。</span> </p><p><span style="font-family: 新細明體,serif;">第</span><span style="font-family: calibri;">&nbsp;&nbsp; 3&nbsp;&nbsp; </span><span style="font-family: 新細明體,serif;">條</span><span style="font-family: calibri;">&nbsp; </span><span style="font-family: 新細明體,serif;">本準則所稱調劑,係指藥事人員自受理處方箋至病患取得藥品間,所為之處方確認、處方登錄、用藥適當性評估、藥品調配或調製、再次核對、確認取藥者交付藥品、用藥指導等相關之行為。</span> </p><p><span style="font-family: 新細明體,serif;">第</span><span style="font-family: calibri;">&nbsp;&nbsp; 4&nbsp;&nbsp; </span><span style="font-family: 新細明體,serif;">條</span><span style="font-family: calibri;">&nbsp; </span><span style="font-family: 新細明體,serif;">本準則所稱藥事作業處所,係指經衛生主管機關核准設立之醫療機構藥劑部門及藥局。</span> </p><p><span style="font-family: 新細明體,serif;">第</span><span style="font-family: calibri;">&nbsp;&nbsp; 5&nbsp;&nbsp; </span><span style="font-family: 新細明體,serif;">條</span><span style="font-family: calibri;">&nbsp; </span><span style="font-family: 新細明體,serif;">本準則所稱調劑處所,係指從事處方調劑、存放處方藥品、調劑器具、設備及其他必要物品之場所。</span> </p><p><span style="font-family: 新細明體,serif;">第</span><span style="font-family: calibri;">&nbsp;&nbsp; 6&nbsp;&nbsp; </span><span style="font-family: 新細明體,serif;">條</span><span style="font-family: calibri;">&nbsp; </span><span style="font-family: 新細明體,serif;">本準則所稱調配,係指調劑作業過程中,依處方箋內容選取正確藥品、計數正確數量、書寫藥袋或貼標籤、包裝等過程之行為。</span> </p><p><span style="font-family: 新細明體,serif;">第</span><span style="font-family: calibri;">&nbsp;&nbsp; 7&nbsp;&nbsp; </span><span style="font-family: 新細明體,serif;">條</span><span style="font-family: calibri;">&nbsp; </span><span style="font-family: 新細明體,serif;">本準則所稱調製,係指調劑作業過程中,依醫師所開具之處方箋,改變原劑型或配製新製品之行為。</span> </p><p><span style="font-family: 新細明體,serif;">第</span><span style="font-family: calibri;">&nbsp;&nbsp; 8&nbsp;&nbsp; </span><span style="font-family: 新細明體,serif;">條</span><span style="font-family: calibri;">&nbsp; </span><span style="font-family: 新細明體,serif;">藥事人員於藥事作業處所,應佩戴執業執照。</span> </p><p><span style="font-family: 新細明體,serif;">第</span><span style="font-family: calibri;">&nbsp;&nbsp; 9&nbsp;&nbsp; </span><span style="font-family: 新細明體,serif;">條</span><span style="font-family: calibri;">&nbsp; </span><span style="font-family: 新細明體,serif;">藥事作業處所應具備洗滌設備。</span> </p><p><span style="font-family: 新細明體,serif;">第</span><span style="font-family: calibri;">&nbsp;&nbsp; 10&nbsp; </span><span style="font-family: 新細明體,serif;">條</span><span style="font-family: calibri;">&nbsp; </span><span style="font-family: 新細明體,serif;">調劑處所應有六平方公尺以上之作業面積,並應與其他作業處所明顯區隔。</span> </p><p><span style="font-family: 新細明體,serif;">前項六平方公尺作業面積,九十一年十月二十一日前設立之藥事作業處所,不適用之。</span> </p><p><span style="font-family: 新細明體,serif;">第</span><span style="font-family: calibri;">&nbsp;&nbsp; 11&nbsp; </span><span style="font-family: 新細明體,serif;">條</span><span style="font-family: calibri;">&nbsp; </span><span style="font-family: 新細明體,serif;">調劑處所應依需要設置藥品專用冷藏冰箱,其內應置溫度計並保持整潔。</span> </p><p><span style="font-family: 新細明體,serif;">第</span><span style="font-family: calibri;">&nbsp;&nbsp; 12&nbsp; </span><span style="font-family: 新細明體,serif;">條</span><span style="font-family: calibri;">&nbsp; </span><span style="font-family: 新細明體,serif;">藥品應依貯存條件存放,避免受到光線直接照射。</span> </p><p><span style="font-family: 新細明體,serif;">疫苗、血液製劑等特殊藥品須分層分櫃,依規定標示及保存。</span> </p><p><span style="font-family: 新細明體,serif;">第</span><span style="font-family: calibri;">&nbsp;&nbsp; 13&nbsp; </span><span style="font-family: 新細明體,serif;">條</span><span style="font-family: calibri;">&nbsp; </span><span style="font-family: 新細明體,serif;">庫存場所應與調劑處所隔離,非經所屬藥事人員許可,不得無故進入。</span> </p><p><span style="font-family: 新細明體,serif;">第</span><span style="font-family: calibri;">&nbsp;&nbsp; 14&nbsp; </span><span style="font-family: 新細明體,serif;">條</span><span style="font-family: calibri;">&nbsp; </span><span style="font-family: 新細明體,serif;">對於已變質或已過保存期限的藥品,應予標示並明顯區隔置放,依法處理。</span> </p><p><span style="font-family: 新細明體,serif;">第</span><span style="font-family: calibri;">&nbsp;&nbsp; 15 &nbsp;</span><span style="font-family: 新細明體,serif;">條</span><span style="font-family: calibri;">&nbsp; </span><span style="font-family: 新細明體,serif;">藥事人員自藥品拆封至調劑之期間,應注意專業包裝藥品之包裝材料及貯存環境,並標示藥名、單位含量及保存期限。</span> </p><p><span style="font-family: 新細明體,serif;">第</span><span style="font-family: calibri;">&nbsp;&nbsp; 16&nbsp; </span><span style="font-family: 新細明體,serif;">條</span><span style="font-family: calibri;">&nbsp; </span><span style="font-family: 新細明體,serif;">處方藥不得以開架式陳列。</span> </p><p><span style="font-family: 新細明體,serif;">第</span><span style="font-family: calibri;">&nbsp;&nbsp; 17&nbsp; </span><span style="font-family: 新細明體,serif;">條</span><span style="font-family: calibri;">&nbsp; </span><span style="font-family: 新細明體,serif;">藥品應於補充前確認其與受補充之藥瓶標示相符,補充後應再次確認。</span> </p><p><span style="font-family: 新細明體,serif;">第</span><span style="font-family: calibri;">&nbsp;&nbsp; 18&nbsp; </span><span style="font-family: 新細明體,serif;">條</span><span style="font-family: calibri;">&nbsp; </span><span style="font-family: 新細明體,serif;">藥事人員受理處方後,應確認處方之合法性、完整性與處方期限有效性。</span> </p><p><span style="font-family: 新細明體,serif;">前項確認處方,應包括下列各項:</span> </p><p><span style="font-family: 新細明體,serif;">一、病患的姓名、年齡、性別及病名。</span> </p><p><span style="font-family: 新細明體,serif;">二、處方醫師姓名、管制藥品使用執照號碼、其簽名或蓋章,所屬醫療機構名稱地址及電話。</span> </p><p><span style="font-family: 新細明體,serif;">三、藥品之名稱、劑型及單位含量。</span> </p><p><span style="font-family: 新細明體,serif;">四、藥品數量。</span> </p><p><span style="font-family: 新細明體,serif;">五、劑量及用藥指示。</span> </p><p><span style="font-family: 新細明體,serif;">六、開立處方日期。</span> </p><p><span style="font-family: 新細明體,serif;">七、連續處方指示。</span> </p><p><span style="font-family: 新細明體,serif;">第二項第七款所稱連續處方指示,包含連續處方的調劑次數及時間間隔。</span> </p><p><span style="font-family: 新細明體,serif;">第</span><span style="font-family: calibri;">&nbsp;&nbsp; 19&nbsp; </span><span style="font-family: 新細明體,serif;">條</span><span style="font-family: calibri;">&nbsp; </span><span style="font-family: 新細明體,serif;">交付藥品之包裝或容器不得重複使用。</span> </p><p><span style="font-family: 新細明體,serif;">為防止兒童取得藥品,藥事人員必要時,應使用有安全瓶蓋之容器。</span> </p><p><span style="font-family: 新細明體,serif;">第</span><span style="font-family: calibri;">&nbsp;&nbsp; 20&nbsp; </span><span style="font-family: 新細明體,serif;">條</span><span style="font-family: calibri;">&nbsp; </span><span style="font-family: 新細明體,serif;">藥事人員應於藥品容器包裝上載明下列事項:</span> </p><p><span style="font-family: 新細明體,serif;">一、病患之姓名及性別。</span> </p><p><span style="font-family: 新細明體,serif;">二、藥品名稱。</span> </p><p><span style="font-family: 新細明體,serif;">三、藥品單位含量及數量。</span> </p><p><span style="font-family: 新細明體,serif;">四、藥品用法及用量。</span> </p><p><span style="font-family: 新細明體,serif;">五、醫療機構或藥局之名稱及地址。</span> </p><p><span style="font-family: 新細明體,serif;">六、調劑者姓名。</span> </p><p><span style="font-family: 新細明體,serif;">七、調劑或交付日期。</span> </p><p><span style="font-family: 新細明體,serif;">下列事項得標示於藥品外包裝容器或列為醫師、藥事人員諮詢事項。</span> </p><p><span style="font-family: 新細明體,serif;">一、警語。</span> </p><p><span style="font-family: 新細明體,serif;">二、主要適應症。</span> </p><p><span style="font-family: 新細明體,serif;">三、主要副作用。</span> </p><p><span style="font-family: 新細明體,serif;">四、醫療機構或藥局之電話號碼。</span> </p><p><span style="font-family: 新細明體,serif;">五、藥品外觀標記其他用藥指示。</span> </p><p><span style="font-family: 新細明體,serif;">第</span><span style="font-family: calibri;">&nbsp;&nbsp; 21&nbsp; </span><span style="font-family: 新細明體,serif;">條</span><span style="font-family: calibri;">&nbsp; </span><span style="font-family: 新細明體,serif;">藥事人員應確保所有藥品在病患治療期間內,均未超過藥品標示之保存期限。</span> </p><p><span style="font-family: 新細明體,serif;">第</span><span style="font-family: calibri;">&nbsp;&nbsp; 22&nbsp; </span><span style="font-family: 新細明體,serif;">條</span><span style="font-family: calibri;">&nbsp; </span><span style="font-family: 新細明體,serif;">藥事人員於交付藥品時,應再次核對標籤內容、藥品種類、數量與處方指示是否正確。</span> </p><p><span style="font-family: 新細明體,serif;">第</span><span style="font-family: calibri;">&nbsp;&nbsp; 23&nbsp; </span><span style="font-family: 新細明體,serif;">條</span><span style="font-family: calibri;">&nbsp; </span><span style="font-family: 新細明體,serif;">藥事人員交付藥品時,應確認所交付之對象為交付處方箋者。</span> </p><p><span style="font-family: 新細明體,serif;">第</span><span style="font-family: calibri;">&nbsp;&nbsp; 24&nbsp; </span><span style="font-family: 新細明體,serif;">條</span><span style="font-family: calibri;">&nbsp; </span><span style="font-family: 新細明體,serif;">醫師依本法第一百零二條之規定得親自為藥品調劑者,準用本準則之有關規定。</span> </p><p><span style="font-family: 新細明體,serif;">第</span><span style="font-family: calibri;">&nbsp;&nbsp; 25&nbsp; </span><span style="font-family: 新細明體,serif;">條</span><span style="font-family: calibri;">&nbsp; </span><span style="font-family: 新細明體,serif;">本準則自發布日施行。</span> </p><p><span style="font-family: calibri;">&nbsp;</span></p><p><span style="font-family: calibri;">&nbsp;</span></p>
發佈日期 2013-12-05
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