Flurpiridaz f-18
Package labels
Loading package label images…
Looking up MedlinePlus…
From MedlinePlus, U.S. National Library of Medicine
Radioactive Diagnostic Agent
Dosing in kidney impairment
Exercise Stress Imaging Once the patient has been positioned on the scanner and respiration has begun to return to normal, begin image acquisition (about 15 minutes to 25 minutes after administration of FLYRCADO). Acquire images for 10 minutes using a scanner in 3D mode. 2.4 Radiation Dosimetry Table 2 shows the estimated radiation absorbed doses per unit of injected activity. [See table below.] Gastrointestinal Tract Stomach Wall 0.04 0.033 0.024 Small Intestine Wall 0.013 0.012 0.014 Upper Large Intestine Wall 0.013 0.012 0.014 Lower Large Intestine Wall 0.012 0.011 0.014 Heart Wall 0.048 0.09 0.039 Kidneys 0.066 0.057 0.027 Liver 0.039 0.044 0.015 Lungs 0.011 0.012 0.012 Muscle 0.01 0.01 0.012 Ovaries 0.012 0.012 0.014 Pancreas 0.016 0.016 0.015 Red Marrow 0.016 0.018 0.015 Salivary Glands 0.035 0.076 0.007 Skin 0.008 0.008 0.009 Spleen 0.016 0.012 0.013 Testes 0.009 0.009 0.011 Thymus 0.011 0.012 0.013 Thyroid 0.032 0.036 0.014 Urinary Bladder Wall 0.023 0.021 0.016 Uterus 0.012 0.012 0.014 Total Body 0.012 0.012 0.012 Effective Dose (mSv/MBq) 0.019 0.019 0.015 The whole-body effective dose resulting from the administration of maximal activity of FLYRCADO of 111 MBq at rest, 241 MBq during pharmacological stress, and 352 MBq during exercise stress is, respectively, 2.1 mSv, 4.6 mSv, and 5.3 mSv.
| Organ | Absorbed Dose per Unit of Administered Activity (mGy/MBq) | ||
|---|---|---|---|
| Rest | Pharmacologic StressThe pharmacologic stress agent used was adenosine. | Exercise Stress | |
| Adrenals | 0.016 | 0.016 | 0.014 |
| Bone surfaces | 0.019 | 0.019 | 0.02 |
| Brain | 0.025 | 0.022 | 0.011 |
| Breasts | 0.009 | 0.009 | 0.01 |
| Gallbladder Wall | 0.017 | 0.018 | 0.015 |
| Gastrointestinal Tract | |||
| Stomach Wall | 0.04 | 0.033 | 0.024 |
| Small Intestine Wall | 0.013 | 0.012 | 0.014 |
| Upper Large Intestine Wall | 0.013 | 0.012 | 0.014 |
| Lower Large Intestine Wall | 0.012 | 0.011 | 0.014 |
| Heart Wall | 0.048 | 0.09 | 0.039 |
| Kidneys | 0.066 | 0.057 | 0.027 |
| Liver | 0.039 | 0.044 | 0.015 |
| Lungs | 0.011 | 0.012 | 0.012 |
| Muscle | 0.01 | 0.01 | 0.012 |
| Ovaries | 0.012 | 0.012 | 0.014 |
| Pancreas | 0.016 | 0.016 | 0.015 |
| Red Marrow | 0.016 | 0.018 | 0.015 |
| Salivary Glands | 0.035 | 0.076 | 0.007 |
| Skin | 0.008 | 0.008 | 0.009 |
| Spleen | 0.016 | 0.012 | 0.013 |
| Testes | 0.009 | 0.009 | 0.011 |
| Thymus | 0.011 | 0.012 | 0.013 |
| Thyroid | 0.032 | 0.036 | 0.014 |
| Urinary Bladder Wall | 0.023 | 0.021 | 0.016 |
| Uterus | 0.012 | 0.012 | 0.014 |
| Total Body | 0.012 | 0.012 | 0.012 |
| Effective Dose (mSv/MBq) | 0.019 | 0.019 | 0.015 |
Preparation and administration
Prepare this dose
Your numbers for flurpiridaz f-18. Take vial strength, diluent, and limits from the label below.
Enter a dose to see draw volume, final concentration, and rates.
Recommended Dosage, Preparation, and Administration Instructions Recommended Dosage The recommended activity for each type of examination is presented in Table 1. Administer two doses by intravenous injection, one for rest imaging and one for stress imaging, using either pharmacologic or exercise stress, in either a 1-day or 2-day protocol.
If performing a combined exercise/pharmacologic stress protocol, administer the recommended activity for pharmacologic stress. When rest and stress imaging are performed on the same day, the recommended minimum stress activity is 2-fold the rest activity for pharmacologic stress and 3-fold the rest activity for exercise stress to provide adequate image quality and obscure residual signal from the first acquisition.
The recommended maximum total volume administered in one day is 6.1 mL. [See table below.] 222 MBq to 241 MBq (6 mCi to 6.5 mCi) 333 MBq to 352 MBq (9 mCi to 9.5 mCi) 2 days 93 MBq to 111 MBq (2.5 mCi to 3 mCi) 93 MBq to 111 MBq (2.5 mCi to 3 mCi) 93 MBq to 111 MBq (2.5 mCi to 3 mCi) Patient Preparation Instruct patients to drink water to ensure adequate hydration prior to administration of FLYRCADO and to continue drinking and voiding frequently during the first hours following administration to reduce radiation exposure [see Warnings and Precautions ] .
Drug Preparation Use aseptic technique and radiation shielding to withdraw and administer FLYRCADO. Calculate the necessary volume to administer based on calibration time and activity using a suitably calibrated instrument. Visually inspect FLYRCADO for particulate matter and discoloration prior to administration and do not use if either is observed.
Ensure the correct syringe is used and has adequate volume (at least 1 mL to 2 mL) so that the activity in the syringe can be administered without excessive dead volume loss. Measure patient dose using a dose calibrator immediately before administration. Do not use and discard FLYRCADO 8 hours after end of synthesis or when the activity falls below the activity requirement at the time of injection, whichever is earlier.
FLYRCADO may be diluted aseptically with 0.9% Sodium Chloride Injection, USP. Diluted product should be used within 8 hours after end of synthesis or when the activity falls below the activity requirement at the time of injection, whichever is earlier. Dispose of unused product in a safe manner and in compliance with applicable regulations.
Administration Instructions Administer FLYRCADO via intravenous injection as a bolus lasting less than 10 seconds and immediately follow with a flush of 0.9% Sodium Chloride Injection, USP. The minimum time between rest and stress dose administration is: 30 minutes when using pharmacologic stress 60 minutes when using exercise stress When using pharmacologic stress, administer FLYRCADO at the time of peak vasodilation according to the prescribing information for the stress agent, using an intravenous port different from the one used for the stress agent.
When using exercise stress, administer FLYRCADO after the patient reaches at least 85% of their age-predicted maximum heart rate or exhibits ischemic signs or symptoms. The patient should then continue to exercise for approximately 1 minute to 2 minutes after the injection. If the patient cannot achieve the target heart rate, the examination may be converted to pharmacologic stress.
Drug interactions
Check interactions
Add the patient's other drugs. Matches come from both FDA labels: by name, drug class, and enzyme or transporter pathway.
- Flurpiridaz f-18
Contraindications
None. None ( 4 )
Safety data
Reported adverse events (FAERS)
Liver injury (LiverTox)
LiverTox has no chapter for flurpiridaz f-18. Check the label's hepatic warnings.
Pregnancy and lactation
Pregnancy
8.1 Pregnancy Risk Summary There are no data on use of flurpiridaz F 18 in pregnant women to evaluate for a drug-associated risk of major birth defects, miscarriage, or other adverse maternal or fetal outcomes. All radiopharmaceuticals, including FLYRCADO, have the potential to cause fetal harm depending on the fetal stage of development and the magnitude of the radiation dose. If considering FLYRCADO administration to a pregnant woman, inform the patient about the potential for adverse pregnancy outcomes based on the radiation dose from flurpiridaz F 18 and the gestational timing of exposure. FLYRCADO contains ethanol (a maximum daily dose of 337 mg anhydrous ethanol).
The lower limit of safety for ethanol use during pregnancy has not been established. Published studies have demonstrated that ethanol is associated with fetal harm including central nervous system abnormalities, behavioral disorders, and impaired intellectual development. If considering FLYRCADO administration to a pregnant woman, inform the patient about the potential for adverse pregnancy outcomes associated with ethanol exposure during pregnancy. The background risk of major birth defects and miscarriage for the indicated population is unknown. All pregnancies have a background risk of birth defect, loss, or other adverse outcomes. In the U.S.
general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively.
For breastfeeding, also see LactMed (National Library of Medicine), which summarizes milk levels and infant effects.
Supply and cost
Drug shortage status
Recalls (last 24 months)
Therapeutic equivalence (Orange Book)
Price ladder
Not the price at the counterThese are not what a patient pays at the pharmacy counter. They are what pharmacies, health plans, and government buyers pay, before manufacturer rebates. A patient's cost depends on their insurance (copay, coinsurance, or deductible) or the pharmacy's cash price.