Drug Interactions between deuruxolitinib and rifampin
This report displays the potential drug interactions for the following 2 drugs:
- deuruxolitinib
- rifampin
Interactions between your drugs
rifAMPin deuruxolitinib
Applies to: rifampin and deuruxolitinib
GENERALLY AVOID: Concomitant use of deuruxolitinib with potent CYP450 3A4 and moderate or potent CYP450 2C9 inducers may significantly decrease the plasma concentrations and therapeutic efficacy of deuruxolitinib. According to the prescribing information, deuruxolitinib is primarily metabolized by CYP450 2C9 (76%) and to a lesser extent by CYP450 3A4 (21%) and 1A2 (3%). Concomitant use of a single dose of deuruxolitinib 12 mg (1.5 times the approved 8 mg dose) with multiple doses of the potent CYP450 3A4 and moderate 2C9 inducer rifampin (600 mg) decreased deuruxolitinib peak plasma concentration (Cmax) and systemic exposure (AUC) by 41% and 78%, respectively.
MANAGEMENT: Use of deuruxolitinib with dual potent CYP450 3A4 and moderate to potent CYP450 2C9 inducers should generally be avoided.
References (1)
- (2024) "Product Information. Leqselvi (deuruxolitinib)." Sun Pharmaceutical Industries
Drug and food/lifestyle interactions
rifAMPin food/lifestyle
Applies to: rifampin
GENERALLY AVOID: Concurrent use of rifampin in patients who ingest alcohol daily may result in an increased incidence of hepatotoxicity. The increase in hepatotoxicity may be due to an additive risk as both alcohol and rifampin are individually associated with this adverse reaction. However, the exact mechanism has not been established.
ADJUST DOSING INTERVAL: Administration with food may reduce oral rifampin absorption, increasing the risk of therapeutic failure or resistance. In a randomized, four-period crossover phase I study of 14 healthy male and female volunteers, the pharmacokinetics of single dose rifampin 600 mg were evaluated under fasting conditions and with a high-fat meal. Researchers observed that administration of rifampin with a high-fat meal reduced rifampin peak plasma concentration (Cmax) by 36%, nearly doubled the time to reach peak plasma concentration (Tmax) but reduced overall exposure (AUC) by only 6%.
MANAGEMENT: The manufacturer of oral forms of rifampin recommends administration on an empty stomach, 30 minutes before or 2 hours after meals. Patients should be encouraged to avoid alcohol or strictly limit their intake. Patients who use alcohol and rifampin concurrently or have a history of alcohol use disorder may require additional monitoring of their liver function during treatment with rifampin.
References (6)
- (2022) "Product Information. Rifampin (rifAMPin)." Akorn Inc
- (2022) "Product Information. Rifampicin (rifampicin)." Mylan Pharmaceuticals Inc
- (2023) "Product Information. Rifadin (rifampicin)." Sanofi
- (2024) "Product Information. Rifadin (rifaMPICin)." Sanofi-Aventis Australia Pty Ltd
- Peloquin CA, Namdar R, Singleton MD, Nix DE (2024) Pharmacokinetics of rifampin under fasting conditions, with food, and with antacids https://pubmed.ncbi.nlm.nih.gov/9925057/
- (2019) "Product Information. Rofact (rifampin)." Bausch Health, Canada Inc.
deuruxolitinib food/lifestyle
Applies to: deuruxolitinib
MONITOR: Smoking during treatment with deuruxolitinib may increase the risk of major adverse cardiovascular events (MACE) and the risk of developing malignancies. In clinical studies of deuruxolitinib, individuals who were current or former smokers had an additional increased risk of overall malignancies. Also, deuruxolitinib may increase patients' risk of MACE, including myocardial infarction, stroke, and cardiovascular death.
MANAGEMENT: Caution is advised if deuruxolitinib is prescribed to current or past smokers. Patients should be informed about the symptoms of serious cardiovascular events and the steps to take if they occur. The manufacturer recommends discontinuing deuruxolitinib in patients that have experienced a myocardial infarction or stroke. Deuruxolitinib may be taken with or without food.
References (1)
- (2024) "Product Information. Leqselvi (deuruxolitinib)." Sun Pharmaceutical Industries
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
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
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