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Drug Interactions between medroxyprogesterone and pralsetinib

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

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Interactions between your drugs

Moderate

medroxyPROGESTERone pralsetinib

Applies to: medroxyprogesterone and pralsetinib

ADDITIONAL CONTRACEPTION RECOMMENDED: Coadministration with pralsetinib may render hormonal contraceptives ineffective. The mechanism for the potential interaction has not been established. In vitro studies indicate that pralsetinib, at clinically relevant concentrations, may be both an inhibitor and inducer of CYP450 3A4, the isoenzyme generally considered responsible for the metabolic clearance of sex hormones (e.g., estrogen, progesterone). Pralsetinib may therefore either decrease clearance via inhibition or increase clearance via induction of this isoenzyme, resulting in increased or decreased plasma concentrations of agents that are metabolized via CYP450 3A4. However, clinical data regarding the use of pralsetinib with hormonal contraceptives are not available. Pralsetinib may also cause fetal harm when administered to a pregnant woman.

MANAGEMENT: Until further data are available, females of reproductive potential should be advised to use effective non-hormonal contraception during treatment and for 2 weeks after the final dose of pralsetinib. In addition, male patients with female partners of reproductive potential should use effective contraception during treatment and for 1 week after the final dose of pralsetinib. Some authorities also recommend using a condom in combination with hormonal contraception if the hormonal method is clinically necessary. Input from a gynecologist or similar expert on adequate contraception, including emergency contraception, should be sought as needed. Intrauterine systems are unlikely to be significantly affected because of their local action.

References (5)
  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
  5. Faculty of Sexual & Reproductive Healthcare Clinical guidance: drug interactions with hormonal contraception https://www.fsrh.org/Common/Uploaded%20files/documents/drug-interactions-with-hormonal-contraception-5may2022.pdf

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.