Drug Interactions between rifapentine and sirolimus protein-bound
This report displays the potential drug interactions for the following 2 drugs:
- rifapentine
- sirolimus protein-bound
Interactions between your drugs
rifapentine sirolimus protein-bound
Applies to: rifapentine and sirolimus protein-bound
GENERALLY AVOID: Coadministration of protein-bound sirolimus intravenous suspension with potent inducers of CYP450 3A4 and/or P-glycoprotein (P-gp) may significantly decrease the systemic exposure to sirolimus, which is a known substrate for both the isoenzyme and efflux transporter. No formal studies evaluating the drug interaction potential of protein-bound sirolimus have been conducted. However, significant decreases in systemic exposure have been reported for oral sirolimus coadministered with potent inducers of CYP450 3A4 and/or P-gp such as rifampin. When a single 20 mg dose of sirolimus oral solution was administered to 14 healthy volunteers following pretreatment with rifampin 600 mg daily for 14 days, mean sirolimus peak blood concentration (Cmax) and systemic exposure (AUC) decreased by 71% and 82%, respectively. Reduced efficacy of protein-bound sirolimus may occur.
MANAGEMENT: Concomitant use of protein-bound sirolimus with potent CYP450 3A4 and/or P-gp inducers should generally be avoided.
References (2)
- (2001) "Product Information. Rapamune (sirolimus)." Wyeth-Ayerst Laboratories
- (2022) "Product Information. Fyarro (sirolimus protein-bound)." Aadi Bioscience, Inc.
Drug and food interactions
rifapentine food
Applies to: rifapentine
ADJUST DOSING INTERVAL: Administration with food may increase the oral bioavailability of rifapentine and reduce the incidence of gastrointestinal adverse events. Administration with a high fat meal typically increases rifapentine's maximum concentration (Cmax) and systemic exposure (AUC) by approximately 40% to 50% over that observed when rifapentine is administered under fasting conditions. Rifapentine is often prescribed in combination with isoniazid. When single doses of rifapentine (900 mg) and isoniazid (900 mg) were administered with a low fat, high carbohydrate breakfast, the Cmax and AUC of rifapentine increased by 47% and 51%, respectively. On the other hand, isoniazid's Cmax and AUC decreased by 46% and 23%, respectively.
MANAGEMENT: Products containing oral rifapentine as the sole ingredient recommend administration with a meal to increase bioavailability and reduce the occurrence of gastrointestinal upset, nausea, and/or vomiting. Consultation of product labeling for combination products and/or relevant guidelines may be helpful if rifapentine is combined with a medication that is typically taken on an empty stomach.
References (2)
- (2021) "Product Information. Isoniazid/Rifapentine 300 mg/300 mg (Macleods) (isoniazid-rifapentine)." Imported (India), 2
- (2021) "Product Information. Priftin (rifapentine)." sanofi-aventis
sirolimus protein-bound food
Applies to: sirolimus protein-bound
GENERALLY AVOID: Coadministration of protein-bound sirolimus intravenous suspension with grapefruit juice may increase the systemic exposure to sirolimus. The proposed mechanism is inhibition of CYP450 3A4-mediated metabolism of sirolimus by certain compounds present in grapefruit. However, grapefruit juice primarily inhibits CYP450 3A4-mediated first-pass metabolism in the gut wall and may have limited effects on medications that are not administered orally. No formal studies evaluating the drug interaction potential of protein-bound sirolimus have been conducted. 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.
MANAGEMENT: The manufacturer recommends avoiding grapefruit and grapefruit juice during treatment with protein-bound sirolimus.
References (1)
- (2022) "Product Information. Fyarro (sirolimus protein-bound)." Aadi Bioscience, 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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