Anpheros Search · Treatment

Fluciclovine (18F)

Also known as: Axumin

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In short

Fluciclovine (18F) is a diagnostic medicinal product indicated in the European Union for Positron Emission Tomography (PET) imaging to detect recurrence of prostate cancer in adult men. This imaging is used when a recurrence is suspected based on elevated blood prostate specific antigen (PSA) levels after primary curative treatment. The medicine has an approved indication for unspecified malignant neoplasms of the prostate.

Source: European Medicines Agency (EMA), Axumin — EPAR, 26/03/2026. © European Medicines Agency. · Source: European Medicines Agency (EMA) — EPAR. © European Medicines Agency.

AI-generated summary of the sources cited on this page, checked automatically against them. Not reviewed by a clinician; not medical advice.

Codes

EMA
EMEA/H/C/004197

Official indications

Quoted unchanged from official product information, in English. Listed alphabetically by product, not ranked.

EMA (EU) Axumin

This medicinal product is for diagnostic use only. Axumin is indicated for Positron Emission Tomography (PET) imaging to detect recurrence of prostate cancer in adult men with a suspected recurrence based on elevated blood prostate specific antigen (PSA) levels after primary curative treatment.

Source: European Medicines Agency (EMA), Axumin — EPAR, 26/03/2026. © European Medicines Agency.

Document date: 26/03/2026 · Official document →

Related terms in the cited sources

Has an official indication for

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What people report

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External resources

Questions

What is Fluciclovine (18F) approved for in the European Union?

This medicinal product is for diagnostic use only. Axumin is indicated for Positron Emission Tomography (PET) imaging to detect recurrence of prostate cancer in adult men with a suspected recurrence based on elevated blood prostate specific antigen (PSA) levels after primary curative treatment. (Source: European Medicines Agency (EMA), Axumin — EPAR, 26/03/2026. © European Medicines Agency.)

Sources and attribution

  • Source: European Medicines Agency (EMA) — EPAR. © European Medicines Agency.
  • Names other than the official source titles: Anpheros translations and plain-language names, made with AI assistance and checked automatically; the source names are in English.
  • This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.
  • Source: European Medicines Agency (EMA), Axumin — EPAR, 26/03/2026. © European Medicines Agency.

Anpheros Search catalog 2026.10.5, published 17 October 2026. About the data →