Drug Interaction Report
2 potential interactions and/or warnings found for the following 2 drugs:
- apalutamide
- Brexafemme (ibrexafungerp)
Interactions between your drugs
apalutamide ibrexafungerp
Applies to: apalutamide, Brexafemme (ibrexafungerp)
GENERALLY AVOID: Coadministration with potent or moderate inducers of CYP450 3A4 may significantly decrease the plasma concentrations of ibrexafungerp, which is primarily metabolized by the isoenzyme in vitro. This interaction has not been studied, but decreased plasma concentrations of ibrexafungerp could theoretically result in treatment failure.
MANAGEMENT: Due to the potential for reduced pharmacologic effects, the concomitant use of ibrexafungerp with potent or moderate CYP450 3A4 inducers should generally be avoided.
References (1)
- (2021) "Product Information. Brexafemme (ibrexafungerp)." SCA Pharmaceuticals (503b)
Drug and food interactions
ibrexafungerp food
Applies to: Brexafemme (ibrexafungerp)
GENERALLY AVOID: Coadministration with grapefruit juice may increase the plasma concentrations of ibrexafungerp. The mechanism is inhibition of CYP450 3A4-mediated first-pass metabolism in the gut wall by certain compounds present in grapefruits. 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. Pharmacokinetic interactions involving grapefruit juice are also subject to a high degree of interpatient variability, thus the extent to which a given patient may be affected is difficult to predict. In healthy subjects receiving the potent CYP450 3A4 inhibitor ketoconazole (400 mg once daily for 15 days), ibrexafungerp peak plasma concentration (Cmax) and systemic exposure (AUC) increased by 2.5-fold and 5.8-fold, respectively. Increased plasma concentrations of ibrexafungerp may increase the risk for adverse effects such as diarrhea, nausea, abdominal pain, dizziness, and vomiting.
When administered to healthy volunteers with a high-fat meal (800 to 1000 calories; 50% fat), ibrexafungerp Cmax and AUC increased 32% and 38%, respectively, compared to fasted conditions.
MANAGEMENT: Ibrexafungerp may be administered with or without food. However, avoiding consumption of grapefruit or grapefruit juice during treatment with ibrexafungerp may be advisable.
References (1)
- (2021) "Product Information. Brexafemme (ibrexafungerp)." SCA Pharmaceuticals (503b)
Therapeutic duplication warnings
No duplication 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.
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. |
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