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Drug Interactions between Mycobutin and rilpivirine

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

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Interactions between your drugs

Major

rifabutin rilpivirine

Applies to: Mycobutin (rifabutin) and rilpivirine

CONTRAINDICATED:: Coadministration with rifabutin may significantly decrease the plasma concentrations of rilpivirine. The proposed mechanism is rifabutin induction of the CYP450 3A4-mediated metabolism of rilpivirine. In 18 study subjects given rilpivirine 25 mg once daily with rifabutin 300 mg once daily, mean rilpivirine peak plasma concentration (Cmax), systemic exposure (AUC) and trough plasma concentration (Cmin) were reduced by 31%, 42% and 48%, respectively. When rilpivirine was given at a higher dosage of 50 mg once daily with rifabutin, mean rilpivirine Cmax and AUC increased by 43% and 16% compared to rilpivirine administered alone at 25 mg once daily, while Cmin decreased by just 7%. The pharmacokinetics of rifabutin and its metabolite, 25-O-desacetylrifabutin, were not significantly altered by rilpivirine.

MANAGEMENT: Given the risk of reduced viral susceptibility and resistance development associated with subtherapeutic antiretroviral drug levels, concomitant use of rilpivirine prolonged-release suspension for injection with rifabutin is considered contraindicated by some authorities. Although not studied, concomitant administration of rifabutin with combination products containing oral rilpivirine is not recommended. However, more recent pharmacokinetic data suggest that oral rilpivirine may be coadministered with rifabutin if the dosage is increased from 25 mg once daily to 50 mg once daily, taken with a meal. Following the discontinuation of rifabutin, the rilpivirine dosage should be decreased to 25 mg once daily.

References (6)
  1. (2023) "Product Information. Mycobutin (rifabutin)." Pfizer Ltd, MY 14_0
  2. (2023) "Product Information. Mycobutin (rifabutin)." Pfizer Australia Pty Ltd, pfpmycoc11223
  3. (2024) "Product Information. Mycobutin (rifabutin)." Pfizer U.S. Pharmaceuticals Group
  4. (2023) "Product Information. Mycobutin (rifabutin)." Pfizer Canada Inc
  5. (2024) "Product Information. Cabenuva 600/900 (cabotegravir-rilpivirine)." ViiV Healthcare
  6. (2024) "Product Information. Edurant (rilpivirine)." Janssen Pharmaceuticals

Drug and food interactions

Moderate

rilpivirine food

Applies to: rilpivirine

GENERALLY AVOID: Coadministration with grapefruit or grapefruit juice may increase the plasma concentrations of rilpivirine. The proposed mechanism is inhibition of CYP450 3A4-mediated first-pass metabolism in the gut wall induced by certain compounds present in grapefruit. In 15 study subjects given rilpivirine (150 mg once daily) with the potent CYP450 3A4 inhibitor ketoconazole (400 mg once daily), mean rilpivirine peak plasma concentration (Cmax), systemic exposure (AUC) and trough plasma concentration (Cmin) were increased by 30%, 49% and 76%, respectively. In 16 study subjects given a single 500 mg dose of a less potent CYP450 3A4 inhibitor chlorzoxazone two hours after rilpivirine (150 mg once daily), mean rilpivirine Cmax, AUC, and Cmin were increased by 17%, 25%, and 18%, respectively. Because grapefruit juice inhibits primarily intestinal rather than hepatic CYP450 3A4, the magnitude of interaction is greatest for those drugs that undergo significant presystemic metabolism by CYP450 3A4 (i.e., drugs with low oral bioavailability). 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.

ADJUST DOSING INTERVAL: The administration of rilpivirine in a fasting state may decrease its oral absorption. Under fasted conditions, the systemic exposure to rilpivirine was 40% lower compared to normal or high-fat caloric meals (533 to 928 Kcal). The systemic exposure was 50% lower when rilpivirine was taken with a protein-rich nutritional beverage.

MANAGEMENT: Coadministration of grapefruit or grapefruit juice with rilpivirine should preferably be avoided. For optimal absorption, it is recommended to take rilpivirine on a regular schedule with a meal.

References (2)
  1. (2011) "Product Information. Edurant (rilpivirine)." Tibotec Pharmaceuticals
  2. Cerner Multum, Inc. (2015) "Canadian Product Information."

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.