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PRECEDEX (dexmedetomidine hydrochloride injection) Patient Counseling Information

17 PATIENT COUNSELING INFORMATION

Precedex is indicated for short-term intravenous sedation. Dosage must be individualized and titrated to the desired clinical effect. Blood pressure, heart rate and oxygen levels will be monitored both continuously during the infusion of Precedex and as clinically appropriate after discontinuation.

When Precedex is infused for more than 6 hours, patients should be informed to report nervousness, agitation, and headaches that may occur for up to 48 hours.
Additionally, patients should be informed to report symptoms that may occur within 48 hours after the administration of Precedex such as: weakness, confusion, excessive sweating, weight loss, abdominal pain, salt cravings, diarrhea, constipation, dizziness or light-headedness.

Manufactured and Distributed by:
Hospira, Inc.
Lake Forest, IL 60045 USA

Licensed from:
Orion Corporation
Espoo, Finland
                                                                                       EN-4272
Hospira, Inc., Lake Forest, IL 60045 USA                                                                                                          Hospira logo

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