Report - DRUG SAFETY UPDATE...患者[10.1参照] 2.8 ナルメフェン塩酸塩水和物を投与中の患者又は投与中止後1週間以内 の患者[10.1参照] 8.2 本剤を投与した際に、悪心、嘔吐、便秘等の症状があらわれることが

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