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Brand Name: Precedex®
Active Ingredient:   dexmedetomidine hydrochloride
Strength(s): 100mcg/mL
Dosage Form(s):   Intravenous injection
Company Name:    Abbott Laboratories
Availability:         Prescription only, intensive care unit use only
*Date Approved by FDA:   December 17, 1999
*Approval by FDA does not mean that the drug is available for consumers at this time.

What is Precedex used for?

Precedex is an intravenous (IV) sedative used only in intensive care unit patients who need manually or mechanically operated medical equipment to keep air flowing into and out of their lungs. Precedex should not be given constantly for more than 24 hours.

How should Precedex be given?

  • Precedex should only be given by health care providers who are skilled in managing patients in an intensive care setting. Because of the action of Precedex, patients on Precedex should be continuously monitored. Significant decreases in blood pressure and slow heartbeat can occur.
  • Precedex is given intravenously (IV) over 24 hours or less using a device that controls the amount of drug that is given.

What should be avoided while taking Precedex?

Precedex should be used with caution in patients who:

  • are pregnant or are breast-feeding
  • have a history of heart-related health problems (e.g., advanced heart block)
  • have a history of liver disease

For more detailed information about Precedex, ask your health care provider.    Link to Precedex's approved label

Date Posted 6/28/00

Back to Drug Side Effects

source: FDA

last update: December 2004

This information is not intended to be a substitute for professional medical advice. You should not use this material to diagnose or treat a health condition or disease without consulting with your healthcare provider.
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