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Drug Interactions between dexamethasone and pralsetinib

This report displays the potential drug interactions for the following 2 drugs:

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Interactions between your drugs

Major

dexAMETHasone pralsetinib

Applies to: dexamethasone and pralsetinib

GENERALLY AVOID: Coadministration with moderate inducers of CYP450 3A4 may significantly decrease the plasma concentrations of pralsetinib, which is primarily metabolized by the isoenzyme. Concurrent use with the moderate CYP450 3A4 inducer efavirenz (600 mg once daily) is predicted to decrease the peak plasma concentration (Cmax) and systemic exposure (AUC) of pralsetinib by 18% and 45%, respectively. Reduced therapeutic efficacy may occur. In addition, when two or more medications with similar side effect profiles are given concurrently, the likelihood of experiencing these adverse reactions may be increased. For example, coadministration with other agents that can lead to elevations in liver transaminases may result in additive effects and an increased risk of hepatotoxicity.

MANAGEMENT: Concomitant use of pralsetinib with moderate CYP450 3A4 inducers should generally be avoided. If coadministration is considered clinically necessary, the current dose of pralsetinib should be increased starting on Day 7 of coadministration with the moderate CYP450 3A4 inducer. The manufacturer recommends increasing the dose of pralsetinib as follows: 600 mg once daily for patients receiving 400 mg once daily, 500 mg once daily for patients receiving 300 mg once daily, and 300 mg once daily for patients receiving 200 mg once daily. Once the moderate CYP450 3A4 inducer has been discontinued for at least 14 days, the pralsetinib dose taken prior to initiating the inducer may be resumed. Patients should be counseled to seek immediate medical attention if they experience symptoms that could indicate serious adverse effects including but not limited to hepatotoxicity. Consult the individual product labeling for further guidance; for example, in instances when the potency of the CYP450 3A4 inducer may be affected by dose or dosage form.

References (4)
  1. (2023) "Product Information. Gavreto (pralsetinib)." Roche Products Pty Ltd, GAVRETO 20230406
  2. (2024) "Product Information. Gavreto (pralsetinib)." Genentech
  3. (2024) "Product Information. Gavreto (pralsetinib)." Roche Products Ltd
  4. (2024) "Product Information. Gavreto (pralsetinib)." Hoffmann-La Roche Limited

Drug and food interactions

Major

pralsetinib food

Applies to: pralsetinib

ADJUST DOSING INTERVAL: Food significantly increases the oral bioavailability of pralsetinib. According to the product labeling, administration of pralsetinib (200 mg) with a high-fat meal (approximately 800 to 1000 calories; 50% to 60% from fat) increased mean pralsetinib peak plasma concentration (Cmax) and systemic exposure (AUC) by 104% and 122%, respectively. The median time to maximum concentration (Tmax) was delayed from 4 hours to 8.5 hours, when compared to the fasted state.

GENERALLY AVOID: The juice of grapefruit and/or Seville oranges may increase the plasma concentrations of pralsetinib. The proposed mechanism is inhibition of CYP450 3A4-mediated first-pass metabolism in the gut wall by certain compounds present in grapefruit and Seville oranges. In general, the effect of grapefruit juice is concentration-, dose- and preparation-dependent, and can vary widely among brands. Certain preparations of grapefruit juice (e.g., high dose, double strength) have sometimes demonstrated potent inhibition of CYP450 3A4, while other preparations (e.g., low dose, single strength) have typically demonstrated moderate inhibition. Increased exposure to pralsetinib may increase the risk of adverse effects such as interstitial lung disease/pneumonitis, liver transaminase elevations, hypertension, and hemorrhage. Some clinical trials have also observed prolongation of the QT interval in patients on pralsetinib, though this was not observed in a study of 34 patients with rearranged during transfection (RET)-altered solid tumors on pralsetinib at the recommended dosage.

MANAGEMENT: Pralsetinib should be administered on an empty stomach, with no food intake recommended for at least 2 hours before and at least 1 hour after taking the medication. Patients should avoid consumption of grapefruit, grapefruit juice, Seville oranges, or Seville orange juice during treatment with pralsetinib.

References (4)
  1. (2023) "Product Information. Gavreto (pralsetinib)." Roche Products Pty Ltd, GAVRETO 20230406
  2. (2024) "Product Information. Gavreto (pralsetinib)." Genentech
  3. (2024) "Product Information. Gavreto (pralsetinib)." Roche Products Ltd
  4. (2024) "Product Information. Gavreto (pralsetinib)." Hoffmann-La Roche Limited

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.


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Drug Interaction Classification

These classifications are only a guideline. The relevance of a particular drug interaction to a specific individual is difficult to determine. Always consult your healthcare provider before starting or stopping any medication.
Major Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit.
Moderate Moderately clinically significant. Usually avoid combinations; use it only under special circumstances.
Minor 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.
Unknown No interaction information available.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.