Label: SODIUM FLUORIDE F 18 injection

  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated July 19, 2014

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  • HIGHLIGHTS OF PRESCRIBING INFORMATION
    These highlights do not include all the information needed to use Sodium Fluoride F 18 Injection USP safely and effectively. See full prescribing information for Sodium Fluoride F 18 Injection USP.
        
    SODIUM FLUORIDE F 18 INJECTION USP
    For Intravenous Use
    Initial U.S. Approval:xxxx

    INDICATIONS AND USAGE

    Sodium Fluoride F 18 Injection USP is a radioactive diagnostic agent for positron emission tomography (PET) indicated for imaging of bone to define areas of altered osteogenic activity (1).  

    DOSAGE AND ADMINISTRATION

    • Sodium Fluoride F 18 Injection USP emits radiation and must be handled with appropriate safety measures (2.1).
    • Administer 300-450 MBq (8-12 mCi) as an intravenous injection in adults (2.4).
    • Administer approximately 2.1 MBq/kg in children with a minimum of 19 MBq (0.5 mCi) and a maximum of 148 MBq (4 mCi) as an intravenous injection (2.5).
    • Imaging can begin 1-2 hours after administration; optimally at one hour post administration (2.7).
    • Encourage patients to void immediately prior to imaging the lumbar spine and bony pelvis (2.7).

    DOSAGE FORMS AND STRENGTHS

    Multiple-dose vial containing 370-3,386 MBq/mL (10-91.5 mCi/mL) of no-carrier-added sodium fluoride F 18 at the end of synthesis (EOS) reference time in aqueous 0.9% sodium chloride solution (3). Sodium Fluoride F 18 Injection USP is a clear, colorless, sterile, pyrogen-free and preservative-free solution for intravenous administration.

    CONTRAINDICATIONS

    None (4)

    WARNINGS AND PRECAUTIONS

    • Allergic Reactions: As with any injectable drug product, allergic reactions and anaphylaxis may occur. Emergency resuscitation equipment and personnel should be immediately available (5.1).
    • Cancer Risk: Sodium Fluoride F 18 Injection USP may increase the risk of cancer. Use of the smallest dose necessary for imaging and ensure safe handling to protect the patient and health care worker (5.2).

    ADVERSE REACTIONS

    No adverse reactions have been reported for based on a review of the published literature, publicly available reference sources, and adverse drug reaction reporting systems (6).



    To report SUSPECTED ADVERSE REACTIONS, contact Division of Nuclear Medicine, Department of Radiology, Mayo Clinic at 507-284-2511 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

    USE IN SPECIFIC POPULATIONS

    • Pregnancy: No human or animal data. Any radiopharmaceutical, including Sodium Fluoride F 18 Injection USP, may cause fetal harm. Use only if clearly needed (8.1).
    • Nursing: A decision should be made whether to interrupt nursing after Sodium Fluoride F 18 Injection USP administration or not to administer Sodium Fluoride F 18 Injection USP taking into consideration the importance of the drug to the mother. (8.3)
    • Pediatrics: Children are more sensitive to radiation and may be at higher risk of cancer from Sodium Fluoride F 18 Injection USP (8.4).

    See 17 for PATIENT COUNSELING INFORMATION.

    Revised: 7/2014

  • Table of Contents

    FULL PRESCRIBING INFORMATION: CONTENTS*

    1       INDICATIONS AND USAGE

    2       DOSAGE AND ADMINISTRATION

    2.1       Radiation Safety – Drug Handling

    2.2       Radiation Safety – Patient Preparation

    2.3       Drug Preparation and Administration

    2.4       Recommended Dose for Adults

    2.5       Recommended Dose for Pediatric Patients

    2.6       Radiation Dosimetry

    2.7       Imaging Guidelines

    3       DOSAGE FORMS AND STRENGTHS

    4       CONTRAINDICATIONS

    5       WARNINGS AND PRECAUTIONS

    5.1       Allergic Reactions

    5.2       Radiation Risks

    6       ADVERSE REACTIONS

    7       DRUG INTERACTIONS

    8       USE IN SPECIFIC POPULATIONS

    8.1       Pregnancy

    8.3       Nursing Mothers

    8.4       Pediatric Use

    11       DESCRIPTION

    11.1       Chemical Characteristics

    11.2       Physical Characteristics

    12       CLINICAL PHARMACOLOGY

    12.1       Mechanism of Action

    12.2       Pharmacodynamics

    12.3       Pharmacokinetics

    13       NONCLINICAL TOXICOLOGY

    13.1       Carcinogenesis, Mutagenesis, Impairment of Fertility

    14       CLINICAL STUDIES

    14.1       Metastatic Bone Disease

    14.2       Other Bone Disorders

    15       REFERENCES

    16       HOW SUPPLIED/STORAGE HANDLING

    17       PATIENT COUNSELING INFORMATION

    17.1       Pre-study Hydration

    17.2       Post-study Voiding

    *
    Sections or subsections omitted from the full prescribing information are not listed.
  • 1       INDICATIONS AND USAGE

    Sodium Fluoride F 18 Injection USP is indicated for diagnostic positron emission tomography (PET) imaging of bone to define areas of altered osteogenic activity.

  • 2       DOSAGE AND ADMINISTRATION

    2.1       Radiation Safety – Drug Handling

    • Wear waterproof gloves and effective shielding when handling Sodium Fluoride F 18 Injection USP. Use appropriate safety measures, including shielding, consistent with proper patient management to avoid unnecessary radiation exposure to the patient, occupational workers, clinical personnel, and other persons.
    • Radiopharmaceuticals should be used by or under the control of physicians who are qualified by specific training and experienced in the safe use and handling of radionuclides, and whose experience and training have been approved by the appropriate governmental agency authorized to license the use of radionuclides.
    • Use aseptic technique to maintain sterility during all operations involved in the manipulation and administration of Sodium Fluoride F 18 Injection USP.
    • The dose of Sodium Fluoride F 18 Injection USP should be minimized consistent with the objectives of the procedure, and the nature of the radiation detection devices employed.
    • The final dose for the patient should be calculated using proper decay factors from the time of End of Synthesis (EOS), and measured by a suitable radioactivity calibration system before administration [see Description (11.2)].

    2.2       Radiation Safety – Patient Preparation

    • To minimize the radiation-absorbed dose to the bladder, encourage adequate hydration. Encourage the patient to ingest at least 500 mL of fluid immediately prior and subsequent to the administration of Sodium Fluoride F 18 Injection USP.
    • Encourage the patient to void one-half hour after administration of Sodium Fluoride F 18 Injection USP and as frequently thereafter as possible for the next 8 hours.

    2.3       Drug Preparation and Administration

    • Calculate the necessary volume to administer based on calibration time and dose.
    • Inspect Sodium Fluoride F 18 Injection USP visually for particulate matter and discoloration before administration, whenever solution and container permits.
    • Do not administer Sodium Fluoride F 18 Injection USP containing particulate matter or discoloration; dispose of these unacceptable or unused preparations in a safe manner, in compliance with applicable regulations.
    • Aseptically withdraw Sodium Fluoride F 18 Injection USP from its container.

    2.4       Recommended Dose for Adults

    Administer 300-450 MBq (8-12 mCi) as an intravenous injection.

    2.5       Recommended Dose for Pediatric Patients

    In reported clinical experience in approximately 100 children, weight-based doses (2.1 MBq/kg) ranging from 19 MBq-148 MBq (0.5 mCi-4 mCi) were used.

    2.6       Radiation Dosimetry

    The age/weight-based estimated absorbed radiation doses (mGy/MBq) from intravenous injection of Sodium Fluoride F 18 Injection USP are shown in Table 1. These estimates were calculated based on human data and using the data published by the Nuclear Regulatory Commission [1] and the International Commission on Radiological Protection for Sodium Fluoride Injection USP [2]. The bone, bone marrow and urinary bladder are considered target and critical organs.

    Table 1: Estimated Absorbed Radiation Does after Intravenous administration of Sodium Fluoride F 18 Injection USP
    OrganEstimated Radiation Dose mGy/MBq
    Adult
    70 kg [1]
    15 year
    56.8 kg [2]
    10 year
    33.2 kg [2]
    5 year
    19.8 kg [2]
    1 year
    9.7 kg [2]
    Adrenals0.00620.0120.0180.0280.052
    Brain0.0056N/AN/AN/AN/A
    Bone surfaces0.0600.0500.0790.130.30
    Breast0.000280.00610.00970.0150.030
    GI
    Gallbladder wall0.0044N/AN/AN/AN/A
    Stomach wall0.00380.0080.0130.0190.036
    Small intestine0.00660.0120.0180.0280.052
    Upper large intestine wall0.00580.0100.0160.0260.046
    Lower large intestine wall0.00120.0160.0250.0370.063
    Heart wall0.0039N/AN/AN/AN/A
    Kidneys0.0190.0250.0360.0530.097
    Liver0.00400.00840.0130.0210.039
    Lungs0.00410.00840.0130.0200.039
    Muscle0.0060N/AN/AN/AN/A
    Ovaries0.0110.0160.0230.0360.063
    Pancreas0.00480.00960.0150.0230.044
    Red marrow0.0280.0530.0.880.180.38
    Skin0.0040N/AN/AN/AN/A
    Spleen 0.00420.00880.0140.0210.041
    Testes0.00780.0130.0210.0330.062
    Thymus0.0035N/AN/AN/AN/A
    Thyroid0.00440.00840.0130.0200.036
    Urinary bladder wall0.250.270.40.611.1
    Uterus0.0190.0230.0370.0570.099
    Other tissueNA0.0100.0150.0240.044
    Effective Dose Equivalent (mSv/MBq)0.0270.0340.0520.0860.17

    [1] Data from Nuclear Regulatory Commission Report, Radiation Dose Estimates for Radiopharmaceuticals, NUREG/CR-6345, page 10, 1996.

    [2] Data from ICRP publication 53, Radiation Dose to Patients from Radiopharmaceuticals, Ann ICRP, Volume 18, pages 15 and 74, 1987.

    2.7       Imaging Guidelines

    • Imaging of Sodium Fluoride F 18 Injection USP can begin 1-2 hours after administration; optimally at 1-hour post-administration.
    • Encourage the patient to void immediately prior to imaging the fluoride F 18 radioactivity in the lumbar spine or bony pelvis.
  • 3       DOSAGE FORMS AND STRENGTHS

    Multiple-dose vial containing 370-3,386 MBq/mL (10-91.5 mCi/mL) at EOS reference time of no-carrier-added sodium fluoride F18 in aqueous 0.9% sodium chloride solution. Sodium Fluoride F 18 Injection USP is a clear, colorless, sterile, pyrogen-free and preservative-free solution for intravenous administration.

  • 4       CONTRAINDICATIONS

    None

  • 5       WARNINGS AND PRECAUTIONS

    5.1       Allergic Reactions

    As with any injectable drug product, allergic reactions and anaphylaxis may occur. Emergency resuscitation equipment and personnel should be immediately available.

    5.2       Radiation Risks

    Sodium Fluoride F 18 Injection USP may increase the risk of cancer. Carcinogenic and mutagenic studies with Sodium Fluoride F 18 Injection USP have not been performed. Use the smallest dose necessary for imaging and ensure safe handling to protect the patient and health care worker [see Dosage and Administration (2.1)].

  • 6       ADVERSE REACTIONS

    No adverse reactions have been reported for Sodium Fluoride F 18 Injection USP based on a review of the published literature, publicly available reference sources, and adverse drug reaction reporting systems. However, the completeness of these sources is not known.

  • 7       DRUG INTERACTIONS

    The possibility of interactions of Sodium Fluoride F 18 Injection USP with other drugs taken by patients undergoing PET imaging has not been studied.

  • 8       USE IN SPECIFIC POPULATIONS

    8.1       Pregnancy

    Pregnancy Category C

    Any radiopharmaceutical including Sodium Fluoride F 18 Injection USP has the potential to cause fetal harm. The likelihood of fetal harm depends on the stage of fetal development, and the radionuclide dose. Animal reproductive and developmental toxicity studies have not been conducted with Sodium Fluoride F 18 Injection USP. Prior to the administration of Sodium Fluoride F 18 Injection USP to women of childbearing potential, assess for presence of pregnancy. Sodium Fluoride F 18 Injection USP should be given to a pregnant woman only if clearly needed.

    8.3       Nursing Mothers

    It is not known whether Sodium Fluoride F 18 Injection USP is excreted into human milk. Because many drugs are excreted in human milk and because of the potential for serious adverse reactions in nursing infants, a decision should be made whether to interrupt nursing after administration of Sodium Fluoride F 18 Injection USP or not to administer Sodium Fluoride F 18 Injection USP, taking into account the importance of the drug to the mother. The body of scientific information related to radioactivity decay, drug tissue distribution and drug elimination shows that less than 0.01% of the radioactivity administered remains in the body after 24 hours (10 half-lives). To minimize the risks to a nursing infant, interrupt nursing for at least 24 hours.

    8.4       Pediatric Use

    In reported clinical experience in approximately 100 children, weight-based doses (2.1 MBq/kg) ranging from 19 MBq-148 MBq (0.5-4 mCi) were used. Sodium Fluoride F 18 was shown to localize to areas of bone turnover including rapidly growing epiphyses in developing long bones. Children are more sensitive to radiation and may be at higher risk of cancer from Sodium Fluoride F 18 injection USP.

  • 11       DESCRIPTION

    11.1       Chemical Characteristics

    Sodium Fluoride F 18 Injection USP is a positron emitting radiopharmaceutical, containing no-carrier-added, radioactive fluoride F 18 that is used for diagnostic purposes in conjunction with PET imaging. It is administered by intravenous injection. The active ingredient, sodium fluoride F 18, has the molecular formula Na[18F] with a molecular weight of 40.99, and has the following chemical structure:

    Na+ 18F 

    Sodium Fluoride F 18 Injection USP is provided as a ready-to-use, isotonic, sterile, pyrogen-free, preservative-free, clear and colorless solution. Each mL of the solution contains between 370 MBq to 3,386 MBq (10 mCi to 91.5 mCi) sodium fluoride F 18, at the EOS reference time, in aqueous 0.9% sodium chloride. The pH of the solution is between 4.5 and 8. The solution is presented in 30 mL multiple-dose glass vials with variable total volume and total radioactivity in each vial.

    11.2       Physical Characteristics

    Fluoride F 18 decays by positron (β+) emission and has a half-life of 109.7 minutes. Ninety-seven percent of the decay results in emission of the positron with a maximum energy of 633 keV and 3% of the decay results in electron capture with subsequent emission of characteristic X-rays of oxygen. The principal photons useful for diagnostic imaging are the 511 keV gamma photons, resulting from the interaction of the emitted positron with an electron (Table 2). Fluorine F 18 atom decays to stable 18O-oxygen.

    Table 2. Principal Emission Data for Fluoride F 18
    Radiation/Emission% per DisintegrationMean Energy
    Positron (β)96.73249.8 keV
    Gamma (±) *193.46511.0 keV

          * Produced by positron annihilation

          [3] Kocher, D.C. Radioactive Decay Data Tables DOE/TIC-11026, 69, 1981.

    The specific gamma ray constant for fluoride F 18 is 5.7 R/hr/mCi (1.35 x 10-6 Gy/hr/kBq) at 1 cm. The half-value layer (HVL) for the 511 keV photons is 4.1 mm lead (Pb). A range of values for the attenuation of radiation results from the interposition of various thickness of Pb. The range of attenuation coefficients for this radionuclide is shown in Table 3. For example, the interposition of an 8.3 mm thickness of Pb with a coefficient of attenuation of 0.25 will decrease the external radiation by 75%.

    Table 3: Radiation Attenuation of 511 keV Photons by Lead (Pb) Shielding
    Shield Thickness (Pb) mmCoefficient of Attenuation
    00.00
    40.50
    80.25
    130.10
    260.01
    390.001
    520.0001

    Table 4 lists the fraction of radioactivity remaining at selected time intervals from the calibration time. This information may be used to correct for physical decay of the radionuclide.

    Table 4: Physical Decay Chart for Fluoride F 18
    Time Since CalibrationFraction Remaining
    0*1.00
    15 minutes0.909
    30 minutes0.826
    60 minutes0.683
    110 minutes0.500
    220 minutes0.250
    440 minutes0.060
    12 hours0.011
    24 hours0.0001

          * Calibration time

  • 12       CLINICAL PHARMACOLOGY

    12.1       Mechanism of Action

    Fluoride F 18 ion normally accumulates in the skeleton in an even fashion, with greater deposition in the axial skeleton (e.g., vertebrae and pelvis) than in the appendicular skeleton and greater disposition in the bones around joints than in the shafts of long bones.

    12.2       Pharmacodynamics

    Increased Fluoride F 18 ion deposition in bone can occur in areas of increased osteogenic activity during growth, infection, malignancy (primary or metastatic) following trauma, or inflammation of bone.

    12.3       Pharmacokinetics

    After intravenous administration, fluoride F 18 ion is rapidly cleared from the plasma in a biexponential manner. The first phase has a half-life of 0.4 h, and the second phase has a half-life of 2.6 h. Essentially all the fluoride F 18 that is delivered to bone by the blood is retained in the bone. One hour after administration of fluoride, F 18 only about 10% of the injected dose remains in the blood. Fluoride F 18 diffuses through capillaries into bone extracellular fluid space, where it becomes bound by chemisorption at the surface of bone crystals, preferentially at sites of newly mineralizing bone.

    Deposition of fluoride F 18 in bone appears to be primarily a function of blood flow to the bone and the efficiency of the bone in extracting the fluoride F 18. Fluoride F 18 does not appear to be bound to serum proteins.

    In patients with normal renal function, 20% or more of the fluorine ion is cleared from the body in the urine within the first 2 hours after intravenous administration.

  • 13       NONCLINICAL TOXICOLOGY

    13.1       Carcinogenesis, Mutagenesis, Impairment of Fertility

    Studies to assess reproductive toxicity, mutagenesis and carcinogenesis potential of Sodium Fluoride F 18 Injection USP have not been performed.

  • 14       CLINICAL STUDIES

    14.1       Metastatic Bone Disease

    The doses used in reported studies ranged from 2.7 mCi to 20 mCi (100 MBq to 740 MBq), with an average median dose of 10 mCi (370 MBq) and an average mean dose of 9.2 mCi (340 MBq). In PET imaging of bone metastases with Sodium Fluoride F 18 Injection USP, focally increased tracer uptake is seen in both osteolytic and osteoblastic bone lesions. Negative PET imaging results with Sodium Fluoride F 18 Injection USP do not preclude the diagnosis of bone metastases. Also, as benign bone lesions are also detected by Sodium Fluoride F 18 Injection USP, positive PET imaging results cannot replace biopsy to confirm a diagnosis of cancer.

    14.2       Other Bone Disorders

    The doses used in reported studies ranged from 2.43 mCi to 15 mCi (90 MBq to 555 MBq), with an average median dose of 8.0 mCi (300 MBq) and an average mean dose of 7.6 mCi (280 MBq).

  • 15       REFERENCES

    1. Stabin M.G., Stubbs J.B. and Toohey R.E. Radiation Dose Estimates for Radiopharmaceuticals, U.S. Nuclear Regulatory Commission report NUREG/CR-6345, page 10, 1996.
    2. Radiation Dose to Patients from Radiopharmaceuticals, ICRP publication 53, Ann ICRP, 18 pages 15 and 74, 1987.
    3. Kocher D.C. “Radioactive Decay Data Tables: A Handbook of decay data for application to radiation dosimetry and radiological assessments” DOE/TIC-11026, page 69, 1981.
  • 16       HOW SUPPLIED/STORAGE HANDLING

    Sodium Fluoride F 18 Injection USP is supplied in a multiple-dose Type I glass vial with elastomeric stopper and aluminum crimp seal containing 370 and 3,386 MBq/mL (10-91.5 mCi/mL) of no carrier-added sodium fluoride F 18, at the EOS reference time, in aqueous 0.9% sodium chloride solution. The total volume and total radioactivity per vial are variable. Each vial is enclosed in a shielded container of appropriate thickness.

    The product is available in a 30-mL vial configuration with a variable fill volume. The NDC number is: 52670-550-30 (30 mL).

    Storage

    Store at 25°C (77°F) in a shielded container; excursions permitted to 15-30°C (59-86°F). Use the solution within 8 hours of the EOS reference time.

    Handling

    Receipt, transfer, handling, possession, or use of this product is subject to the radioactive material regulations and licensing requirements of the U.S. Nuclear Regulatory Commission, Agreement States or Licensing States as appropriate.

  • 17       PATIENT COUNSELING INFORMATION

    17.1       Pre-study Hydration

    Encourage patients to drink at least 500 mL of water prior to drug administration.

    17.2       Post-study Voiding

    To help protect themselves and others in their environment, patients should take the following precautions for 8 hours after injection; whenever possible, use a toilet and flush several times after each use; wash hands thoroughly after each voiding or fecal elimination. If blood, urine or feces soil clothing, wash the clothing separately.

    Manufactured by:
    Mayo Clinic PET Radiochemistry Facility
    200 1st St SW
    Rochester, MN 55905

    Mayo Clinic PET Radiochemistry Facility
    5861 E Mayo Blvd
    Phoenix, AZ 85054

    Distributed by:
    Mayo Clinic PET Radiochemistry Facility
    200 1st St SW
    Rochester, MN 55905

    Mayo Clinic PET Radiochemistry Facility
    5861 E Mayo Blvd
    Phoenix, AZ 85054

  • PRINCIPAL DISPLAY PANEL

    NDC 52670-550-30
    SODIUM FLUORIDE F 18 INJECTION, USP
    For Intravenous Use Rx Only

    PRINCIPAL DISPLAY PANEL
NDC 52670-550-30
SODIUM FLUORIDE F 18 INJECTION, USP
For Intravenous Use Rx Only

  • INGREDIENTS AND APPEARANCE
    SODIUM FLUORIDE F 18 
    sodium fluoride f 18 injection
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:52670-550
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM FLUORIDE F-18 (UNII: 9L75099X6R) (FLUORIDE ION F-18 - UNII:4M4WE5N2GE) FLUORIDE ION F-1891.5 mCi  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52670-550-3030 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product06/28/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA20360506/28/2013
    Labeler - Mayo Clinic (167141923)