Drug Interactions between AccessPak for HIV PEP Basic and cabozantinib
This report displays the potential drug interactions for the following 2 drugs:
- AccessPak for HIV PEP Basic (emtricitabine/tenofovir disoproxil)
- cabozantinib
Interactions between your drugs
tenofovir cabozantinib
Applies to: AccessPak for HIV PEP Basic (emtricitabine / tenofovir disoproxil) and cabozantinib
MONITOR: Coadministration of cabozantinib with multidrug resistance-associated proteins (MRP2) inhibitors may increase exposure and toxicity of cabozantinib. In vitro studies have shown MRP2 inhibitors may increase the plasma concentrations of cabozantinib, a MRP2 substrate. The clinical relevance of this finding is not known.
MANAGEMENT: Caution is advised if cabozantinib is used concomitantly with a MRP2 inhibitor. Monitor for cabozantinib toxicity, such as gastrointestinal perforations and fistulas, hemorrhage, thrombotic events, hypertension, diarrhea, and palmar-plantar erythrodysesthesia. Dose reductions, interruption or discontinuation of cabozantinib may be necessary if toxicity occurs.
References (4)
- Cerner Multum, Inc. "UK Summary of Product Characteristics."
- Cerner Multum, Inc. "Australian Product Information."
- (2012) "Product Information. Cometriq (cabozantinib)." Exelixis Inc
- (2016) "Product Information. Cabometyx (cabozantinib)." Exelixis Inc
emtricitabine cabozantinib
Applies to: AccessPak for HIV PEP Basic (emtricitabine / tenofovir disoproxil) and cabozantinib
MONITOR: Coadministration of cabozantinib with multidrug resistance-associated proteins (MRP2) inhibitors may increase exposure and toxicity of cabozantinib. In vitro studies have shown MRP2 inhibitors may increase the plasma concentrations of cabozantinib, a MRP2 substrate. The clinical relevance of this finding is not known.
MANAGEMENT: Caution is advised if cabozantinib is used concomitantly with a MRP2 inhibitor. Monitor for cabozantinib toxicity, such as gastrointestinal perforations and fistulas, hemorrhage, thrombotic events, hypertension, diarrhea, and palmar-plantar erythrodysesthesia. Dose reductions, interruption or discontinuation of cabozantinib may be necessary if toxicity occurs.
References (4)
- Cerner Multum, Inc. "UK Summary of Product Characteristics."
- Cerner Multum, Inc. "Australian Product Information."
- (2012) "Product Information. Cometriq (cabozantinib)." Exelixis Inc
- (2016) "Product Information. Cabometyx (cabozantinib)." Exelixis Inc
Drug and food interactions
cabozantinib food
Applies to: cabozantinib
ADJUST DOSING INTERVAL: Food may alter the oral bioavailability of cabozantinib. When healthy subjects were given a single 140 mg oral dose with a high-fat meal, cabozantinib peak plasma concentration (Cmax) and systemic exposure (AUC) increased by 41% and 57%, respectively, relative to administration under fasting conditions. In clinical studies, patients were administered cabozantinib without food.
GENERALLY AVOID: Coadministration with grapefruit juice is likely to increase the plasma concentrations of cabozantinib, which is primarily metabolized by CYP450 3A4. However, the interaction has not been studied. The proposed mechanism is inhibition of CYP450 3A4-mediated first-pass metabolism in the gut wall by certain compounds present in grapefruit.
MANAGEMENT: Cabozantinib should be administered at least one hour before or two hours after a meal. The consumption of grapefruit, grapefruit juice, and supplements that contain grapefruit extract should be avoided.
References (1)
- (2012) "Product Information. Cometriq (cabozantinib)." Exelixis Inc
tenofovir food
Applies to: AccessPak for HIV PEP Basic (emtricitabine / tenofovir disoproxil)
Food enhances the oral absorption and bioavailability of tenofovir, the active entity of tenofovir disoproxil fumarate. According to the product labeling, administration of the drug following a high-fat meal increased the mean peak plasma concentration (Cmax) and area under the concentration-time curve (AUC) of tenofovir by approximately 14% and 40%, respectively, compared to administration in the fasting state. However, administration with a light meal did not significantly affect the pharmacokinetics of tenofovir compared to administration in the fasting state. Food delays the time to reach tenofovir Cmax by approximately 1 hour. Tenofovir disoproxil fumarate may be administered without regard to meals.
References (1)
- (2001) "Product Information. Viread (tenofovir)." Gilead Sciences
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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