Drug Interactions between rufinamide and ruxolitinib topical
This report displays the potential drug interactions for the following 2 drugs:
- rufinamide
- ruxolitinib topical
Interactions between your drugs
rufinamide ruxolitinib topical
Applies to: rufinamide and ruxolitinib topical
Coadministration with inducers of CYP450 3A4 may decrease plasma concentrations (Cmax) and systemic exposure (AUC) of topical ruxolitinib, which is primarily metabolized by the isoenzyme. Following administration of rifampin (600 mg once daily for 10 days), a potent CYP450 3A4 inducer, healthy subjects then received a single dose of ruxolitinib (50 mg orally). The Cmax and AUC of ruxolitinib decreased 32% and 61% respectively, compared to healthy subjects receiving the oral ruxolitinib dose alone. However, the clinical significance of this effect on a topical formulation is unknown. Consultation with individual package labeling, as well as relevant institutional protocols, may be advisable for further guidance. Clinical data for less potent inducers are not available.
References (2)
- (2024) "Product Information. Opzelura (ruxolitinib topical)." Incyte Corporation
- (2024) "Product Information. Opzelura (ruxolitinib topical)." Incyte Corporation, 2
Drug and food interactions
ruxolitinib topical food
Applies to: ruxolitinib topical
MONITOR CLOSELY: Smoking during treatment with topical ruxolitinib may increase the risk of major adverse cardiovascular events (MACE) and the risk of developing malignancies, including lymphomas. During clinical trials, patients who were current or past smokers and received oral Janus Kinase (JAK) inhibitors to treat inflammatory conditions had an additional increased risk of overall malignancies. Additionally, oral JAK inhibitors reportedly increase patients' risk of MACE, including cardiovascular death, myocardial infarction, and stroke, particularly in patients who are current or past smokers or patients with other cardiovascular risk factors.
MANAGEMENT: The potential risks and benefits of topical ruxolitinib should be carefully weighed prior to initiating therapy, particularly in patients with cardiovascular risk factors, as well as those with a history of malignancy, those who develop a malignancy while on treatment, and/or patients who are 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 topical ruxolitinib in patients who have experienced a myocardial infarction or stroke.
References (2)
- (2024) "Product Information. Opzelura (ruxolitinib topical)." Incyte Corporation
- (2024) "Product Information. Opzelura (ruxolitinib topical)." Incyte Corporation, 2
rufinamide food
Applies to: rufinamide
GENERALLY AVOID: Alcohol may potentiate some of the pharmacologic effects of rufinamide. Use in combination may result in additive central nervous system depression and/or impairment of judgment, thinking, and psychomotor skills.
ADJUST DOSING INTERVAL: Food enhances the oral absorption and bioavailability of rufinamide. In healthy volunteers, administration of a single 400 mg dose of rufinamide with food resulted in an approximately 56% increase in mean peak plasma concentration (Cmax) and a 34% increase in systemic exposure (AUC) compared to administration during a fasting state.
MANAGEMENT: To ensure maximal oral absorption, it is preferable to administer rufinamide with food. Patients receiving rufinamide should be advised to avoid consumption of alcohol. Ambulatory patients should be counseled to avoid hazardous activities requiring complete mental alertness and motor coordination until they know how rufinamide affects them, and to notify their physician if they experience excessive or prolonged CNS effects that interfere with their normal activities.
References (1)
- (2008) "Product Information. Banzel (rufinamide)." Eisai 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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