Axumin

Active Ingredient(s): Fluciclovine
FDA Approved: * May 27, 2016
Pharm Company: * BLUE EARTH DIAGNOSTICS LTD
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".



Axumin Overview

Fluciclovine (18F), also known as anti-1-amino-3-18F-fluorocyclobutane-1-carboxylic acid (anti-3[18F] FACBC),[1][2] or as Axumin (brand name), is a diagnostic agent indicated for positron emission tomography (PET) imaging in men with suspected prostate cancer recurrence based on elevated prostate specific antigen (PSA) levels.[3][4] Contents 1 Background 2 Mechanism 3 Marketing 4 References 5 External links Background Most...

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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: en.wikipedia.org/wiki/Fluciclovine

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Possible Dosages for this and Related Drugs:

Fluciclovine
  • Injection: 335-8200 Mbq/ml (9-221 Mci/ml)
  • Solution: 9-221mci/ml
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Axumin: (1 result)

Sorted by National Drug Code
  • 69932-001 Axumin 221 mci/Ml Intravenous Injection, Solution by Blue Earth Diagnostics

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