Drug Interactions between betiatide and encorafenib
This report displays the potential drug interactions for the following 2 drugs:
- betiatide
- encorafenib
Interactions between your drugs
encorafenib betiatide
Applies to: encorafenib and betiatide
MONITOR: The administration of an organic anion transporter 1 (OAT1) inhibitor just prior to or concurrently with the radiopharmaceutical, technetium (Tc99m) mertiatide, may reduce its renal uptake and excretion as it is a substrate of this transporter. Delayed clearance could result in a misinterpretation of diagnostic study results. Clinical data is limited. One crossover study conducted in 12 healthy male volunteers (22-25 years old), compared the results of Tc99m mertiatide injection alone to those obtained after the subjects received a potent OAT1 inhibitor (probenecid 750 mg) 1 hour prior to the radiopharmaceutical injection. Probenecid administration prolonged the plasma clearance half-life of Tc99m mertiatide in the late phase (30-60 minutes post injection), from 24.4 +/- 9.9 minutes to 33.1 +/- 12.9 minutes. Similarly, the volunteer's Tc99m mertiatide blood concentrations were higher after treatment with probenecid, suggesting that renal excretion of the radiopharmaceutical was inhibited by the OAT1 inhibitor.
MANAGEMENT: Administration of an organic anion transporter 1 (OAT1) inhibitor just prior to or concurrently with technetium (Tc99m) mertiatide should be done with caution as it may delay excretion of the radiopharmaceutical and affect the efficacy of the diagnostic procedure. Dehydration and acidosis can also lead to prolonged elimination of Tc99m mertiatide, further impacting the efficacy of the diagnostic test. Refer to the product labeling or local protocols for guidelines on patient hydration.
References (2)
- (2019) "Product Information. IELMAG3 (mertiatide)." Xiel Ltd
- Takahara N, Saga T, Inubushi M, et al. (2013) "Drugs interacting with OAT-1 affect uptake of Tc-99m-mercaptoacetyl-triglycine (MAG3) in the human kidney: Therapeutic drug interaction in Tc-99m-MAG3 diagnosis of renal function and possible application of Tc-99m-MAG3 for drug development" Nucl Med Biol, 40, p. 643-50
Drug and food interactions
encorafenib food
Applies to: encorafenib
GENERALLY AVOID: Coadministration with potent or moderate inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of encorafenib, which is primarily metabolized by the isoenzyme. When a single 50 mg dose of encorafenib (equivalent to 0.1 times the recommended dose) was administered with posaconazole, a potent CYP450 3A4 inhibitor, encorafenib peak plasma concentration (Cmax) increased by 68% and systemic exposure (AUC) increased by 3-fold. When the same dose of encorafenib was administered with diltiazem, a moderate CYP450 3A4 inhibitor, encorafenib Cmax increased by 45% and AUC increased by 2-fold. Increased exposure to encorafenib may increase the risk of serious and life-threatening adverse effects such as hemorrhage, uveitis, QT prolongation, hepatotoxicity, dermatologic reactions, and new malignancies.
MANAGEMENT: Concomitant use of encorafenib with grapefruit or grapefruit juice should generally be avoided. If coadministration is required, the manufacturer recommends reducing the encorafenib dose to one-third of the dose used prior to addition of a potent CYP450 3A4 inhibitor or one-half of the dose used prior to addition of a moderate CYP450 3A4 inhibitor. After the inhibitor has been discontinued for 3 to 5 elimination half-lives, the encorafenib dose that was taken prior to initiating the inhibitor may be resumed.
References (1)
- (2018) "Product Information. Braftovi (encorafenib)." Array BioPharma Inc.
Therapeutic duplication warnings
No warnings were found for your selected drugs.
Therapeutic duplication warnings are only returned when drugs within the same group exceed the recommended therapeutic duplication maximum.
See also
Drug Interaction Classification
Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit. | |
Moderately clinically significant. Usually avoid combinations; use it only under special circumstances. | |
Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan. | |
No interaction information available. |
Further information
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