The purpose of this study is to look at the safety of Precedex when it was used to calm children at procedures or tests under actual medical practice in Japan. This study is seeking for children who are 1 month to less than 18 years old. The patients are planned to be looked over: * From the time of patient check before receiving Precedex * To 1 hour after the completion or stop of using Precedex.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Number of participants with adverse drug reactions (ADRs)
Timeframe: From the time of patient assessment before the start of administration of Precedex to 1 hour after the completion or discontinuation of administration