Florbetaben f-18

FDA label, Lantheus Biosciences Ltd., a Lantheus company, intravenous, effective 2026-07-24. Full label on DailyMed

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From MedlinePlus, U.S. National Library of Medicine

Quoted from the FDA label. Product labels differ by manufacturer and change over time; confirm against the label for the product you are using.

Radioactive Diagnostic Agent

Dosing in kidney impairment

Table 1 Estimated Radiation Absorbed Doses from Intravenous Injection of Neuraceq
Organ/TissueMean Absorbed Radiation Dose per Unit Administered Activity [microGy/MBq]
Adrenals13
Brain13
Breasts7
Gallbladder Wall137
Heart Wall14
Kidneys24
Liver39
Lower Large Intestine-Wall35
Lungs15
Muscle10
Osteogenic Cells15
Ovaries16
Pancreas14
Red Marrow12
Skin7
Small Intestine31
Spleen10
Stomach Wall12
Testes9
Thymus9
Thyroid8
Upper Large Intestine-Wall38
Urinary Bladder Wall70
Uterus16
Total Body11
Effective Dose (microSv/MBq)19
Table 1 Estimated Radiation Absorbed Doses from Intravenous Injection of Neuraceq
Organ/TissueMean Absorbed Radiation Dose per Unit Administered Activity [microGy/MBq]
Adrenals13
Brain13
Breasts7
Gallbladder Wall137
Heart Wall14
Kidneys24
Liver39
Lower Large Intestine-Wall35
Lungs15
Muscle10
Osteogenic Cells15
Ovaries16
Pancreas14
Red Marrow12
Skin7
Small Intestine31
Spleen10
Stomach Wall12
Testes9
Thymus9
Thyroid8
Upper Large Intestine-Wall38
Urinary Bladder Wall70
Uterus16
Total Body11
Effective Dose (microSv/MBq)19

Preparation and administration

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Recommended Dosing and Administration Instructions Recommended Dosage The recommended amount of radioactivity of NEURACEQ is 300 MBq (8.1 mCi) in a total volume of up to 10 mL, administered as a single slow intravenous bolus (6 sec/mL). The maximum mass dose is 30 micrograms. Follow the administration with an intravenous flush of approximately 10 mL of 0.9% sodium chloride injection.

Patient Preparation Instruct patients to hydrate before and after NEURACEQ administration and to void before imaging and frequently thereafter following NEURACEQ administration [see Warnings and Precautions ] . Administration Use aseptic technique and radiation shielding to withdraw and administer NEURACEQ. Visually inspect NEURACEQ for particulate matter and discoloration prior to administration.

Do not use NEURACEQ if it contains particulate matter or if it is discolored. Do not dilute NEURACEQ. Measure the activity of NEURACEQ with a dose calibrator immediately prior to injection. Verify patency of the indwelling catheter by a test flush with 0.9% sodium chloride injection prior to administration of NEURACEQ. Dispose of unused product in a safe manner in compliance with applicable regulations

Recommended Dosing and Administration Instructions Recommended Dosage The recommended amount of radioactivity of NEURACEQ is 300 MBq (8.1 mCi) in a total volume of up to 10 mL, administered as a single slow intravenous bolus (6 sec/mL). The maximum mass dose is 30 micrograms. Follow the administration with an intravenous flush of approximately 10 mL of 0.9% sodium chloride injection.

Patient Preparation Instruct patients to hydrate before and after NEURACEQ administration and to void before imaging and frequently thereafter following NEURACEQ administration [see Warnings and Precautions ] . Administration Use aseptic technique and radiation shielding to withdraw and administer NEURACEQ. Visually inspect NEURACEQ for particulate matter and discoloration prior to administration.

Do not use NEURACEQ if it contains particulate matter or if it is discolored. Do not dilute NEURACEQ. Measure the activity of NEURACEQ with a dose calibrator immediately prior to injection. Verify patency of the indwelling catheter by a test flush with 0.9% sodium chloride injection prior to administration of NEURACEQ. Dispose of unused product in a safe manner in compliance with applicable regulations

Contraindications

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