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Trade names | Fluorodopa F18 |
Other names | 6-fluoro-L-DOPA, FDOPA |
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Routes of administration | Intravenous |
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Formula | C9H10FNO4 |
Molar mass | 214.18 g·mol−1 |
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Fluorodopa, also known as FDOPA, is a fluorinated form of L-DOPA primarily synthesized as its fluorine-18 isotopologue for use as a radiotracer in positron emission tomography (PET). [1]
The most common side effects are injection site pain. [2]
Fluorodopa is indicated for use in positron emission tomography (PET) to visualize dopaminergic nerve terminals in the striatum for the evaluation of adults with suspected Parkinsonian syndromes (PS). [2]
In October 2019, Fluorodopa was approved in the United States for the visual detection of certain nerve cells in adult patients with suspected Parkinsonian Syndromes (PS). [3] [4]
The U.S. Food and Drug Administration (FDA) approved Fluorodopa F 18 based on evidence from one clinical trial of 56 patients with suspected PS. [3] The trial was conducted at one clinical site in the United States. [3]
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