Drug Interactions between boceprevir and escitalopram
This report displays the potential drug interactions for the following 2 drugs:
- boceprevir
- escitalopram
Interactions between your drugs
escitalopram boceprevir
Applies to: escitalopram and boceprevir
MONITOR: Coadministration with the hepatitis C virus (HCV) NS3/4A protease inhibitors, boceprevir and telaprevir, may decrease the plasma concentrations of escitalopram. The mechanism of interaction has not been described. When a single 10 mg dose of escitalopram was given in combination with boceprevir (800 mg three times a day for 11 days), mean escitalopram peak plasma concentration (Cmax) and systemic exposure (AUC) decreased by approximately 20% each. Likewise, in 13 study subjects, administration of escitalopram (10 mg once daily for 7 days) in combination with telaprevir (750 mg every 8 hours for 14 days) decreased escitalopram Cmax, AUC and trough plasma concentration (Cmin) by an average of 30%, 35% and 42%, respectively, compared to administration alone. Escitalopram had no significant effect on the pharmacokinetics of boceprevir or telaprevir.
MANAGEMENT: The possibility of diminished therapeutic effects should be considered when escitalopram is used in combination with boceprevir or telaprevir. Pharmacologic response to escitalopram should be closely monitored and the dosage adjusted, if necessary, following the initiation or discontinuation of the HCV protease inhibitor.
References
- (2011) "Product Information. Victrelis (boceprevir)." Schering-Plough Corporation
- (2011) "Product Information. Incivek (telaprevir)." Vertex Pharmaceuticals
Drug and food interactions
escitalopram food
Applies to: escitalopram
GENERALLY AVOID: Alcohol may potentiate some of the pharmacologic effects of CNS-active agents. Use in combination may result in additive central nervous system depression and/or impairment of judgment, thinking, and psychomotor skills.
MANAGEMENT: Patients receiving CNS-active agents should be warned of this interaction and advised to avoid or limit consumption of alcohol. Ambulatory patients should be counseled to avoid hazardous activities requiring complete mental alertness and motor coordination until they know how these agents affect them, and to notify their physician if they experience excessive or prolonged CNS effects that interfere with their normal activities.
References
- Warrington SJ, Ankier SI, Turner P (1986) "Evaluation of possible interactions between ethanol and trazodone or amitriptyline." Neuropsychobiology, 15, p. 31-7
- Gilman AG, eds., Nies AS, Rall TW, Taylor P (1990) "Goodman and Gilman's the Pharmacological Basis of Therapeutics." New York, NY: Pergamon Press Inc.
- (2012) "Product Information. Fycompa (perampanel)." Eisai Inc
- (2015) "Product Information. Rexulti (brexpiprazole)." Otsuka American Pharmaceuticals Inc
boceprevir food
Applies to: boceprevir
ADJUST DOSING INTERVAL: Food significantly enhances the oral bioavailability of boceprevir. When given at 800 mg three times daily with food, boceprevir exposure increased by up to 65% relative to administration in the fasting state. The bioavailability of boceprevir was similar regardless of meal type (e.g., high-fat versus low-fat) or whether taken 5 minutes prior to eating, during a meal, or immediately following completion of the meal. Therefore, boceprevir may be taken without regard to either meal type or timing of the meal.
MANAGEMENT: To ensure maximal oral absorption, boceprevir should be administered with a meal or light snack.
References
- (2011) "Product Information. Victrelis (boceprevir)." Schering-Plough Corporation
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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