Cerianna Side Effects
Generic name: fluoroestradiol F 18
Medically reviewed by Drugs.com. Last updated on Aug 16, 2024.
Note: This document provides detailed information about Cerianna Side Effects associated with fluoroestradiol F 18. Some dosage forms listed on this page may not apply specifically to the brand name Cerianna.
Applies to fluoroestradiol F 18: intravenous solution.
Common side effects of Cerianna
Some side effects of fluoroestradiol F 18 may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects.
Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:
Rare side effects
- change in or loss of taste
- pain, redness, or irritation at the injection site
Serious side effects of Cerianna
Along with its needed effects, fluoroestradiol F 18 (the active ingredient contained in Cerianna) may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.
For healthcare professionals
Applies to fluoroestradiol F 18: intravenous solution.
Local adverse events
- Frequency not reported: Injection-site pain[Ref]
Injection-site pain was experienced in less than 1% of patients.[Ref]
Nervous system
- Frequency not reported: Dysgeusia[Ref]
Dysgeusia was experienced in less than 1% of patients.[Ref]
References
1. (2022) "Product Information. Cerianna (fluoroestradiol F 18)." GE Healthcare
More about Cerianna (fluoroestradiol F 18)
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- Drug class: diagnostic radiopharmaceuticals
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Further information
Cerianna side effects can vary depending on the individual. Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
Note: Medication side effects may be underreported. If you are experiencing side effects that are not listed, submit a report to the FDA by following this guide.