Active Ingredient(s): Gadobutrol
FDA Approved: * March 14, 2011
Category: Diagnostic Aid

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".

Gadavist Overview

Gadobutrol (INN) (Gd-DO3A-butrol) is a gadolinium-based MRI contrast agent (GBCA). It received marketing approval in Canada and the United States.[1][2][3][4] As of 2007, it was the only GBCA approved at 1.0 molar concentrations.[5] Gadobutrol is marketed by Bayer AG as Gadovist, and by Bayer HealthCare Pharmaceuticals as Gadavist.[6] Contents 1 Medical uses 2 Adverse effects 3 Use in specific po...

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Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source:

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Possible Dosages for this and Related Drugs:

  • Injection: 1mmol/ml
  • Solution: 1.20944gm/2ml (604.72mg/ml), 18.1416gm/30ml (604.72mg/ml), 39.3068gm/65ml (604.72mg/ml), 4.5354gm/7.5ml (604.72mg/ml), 6.0472gm/10ml (604.72mg/ml), 9.0708gm/15ml (604.72mg/ml)
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Gadavist: (1 result)

Sorted by National Drug Code
  • 50419-325 Gadavist 604.72 mg/ml Intravenous Injection by Bayer Healthcare Pharmaceuticals Inc.

Other drugs which contain Gadobutrol or a similar ingredient: (1 result)

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This information has been independently compiled and is for informational purposes only. It is not intended to be a substitute for medical advice from a qualified healthcare professional; nor is it intended to diagnose, treat, cure or prevent any disease. For more details please see the Medical Disclaimer. This page was last updated on 9 August 2020.

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