Drug Interactions between elderberry / melatonin and pazopanib
This report displays the potential drug interactions for the following 2 drugs:
- elderberry/melatonin
- pazopanib
Interactions between your drugs
PAZOPanib elderberry
Applies to: pazopanib and elderberry / melatonin
MONITOR: Coadministration of elderberry and pazopanib may increase the risk of pazopanib-related adverse effects. This interaction was suspected in a case report involving a 65-year-old woman diagnosed with localized intermediate-grade sarcoma initiated on pazopanib 400 mg orally daily while taking elderberry supplements at an unknown dose. Pazopanib was increased to 800 mg orally daily after one week. By week three on pazopanib, the patient reported intense nausea and frequent loose stools, requiring treatment and by the fourth week, laboratory tests indicated grade 3 liver injury. All medications, including elderberry supplements, were stopped and within four weeks, liver enzymes returned to baseline. At this time, pazopanib treatment was resumed at a lower dosage of 400 mg orally daily without the recurrence of adverse effects or liver injury. Although clinical evidence is limited, the potential mechanism for this interaction may be due to elderberry mediated inhibition of CYP450 3A4 which may occur at higher doses and lead to increased pazopanib exposure.
MANAGEMENT: Caution is advised if elderberry is used concomitantly with pazopanib. If coadministration is required, patients should be more closely monitored for pazopanib-related adverse effects such as hepatotoxicity, nausea, vomiting, and diarrhea.
References (1)
- Agarwal N, Mangla A (2024) "Elderberry interaction with pazopanib in a patient with soft tissue sarcoma: A case report and literature review" Mol Clin Oncol, 20, p. 1-5
Drug and food interactions
PAZOPanib food
Applies to: pazopanib
GENERALLY AVOID: Grapefruit juice may increase the plasma concentrations of pazopanib. The proposed mechanism is inhibition of CYP450 3A4-mediated first-pass metabolism in the gut wall by certain compounds present in grapefruits. Although not studied, the interaction may increase the risk of QT interval prolongation and torsade de pointes arrhythmia as well as severe and fatal hepatotoxicity associated with the use of pazopanib.
ADJUST DOSING INTERVAL: Food increases the oral bioavailability of pazopanib. The mechanism of interaction is unknown. Administration of pazopanib with a high-fat or low-fat meal results in an approximately 2-fold increase in peak plasma concentration (Cmax) and systemic exposure (AUC).
MANAGEMENT: Patients treated with pazopanib should avoid consumption of grapefruit, grapefruit juice, and any supplement containing grapefruit extract. Pazopanib should be administered at least one hour before or two hours after a meal.
References (1)
- (2009) "Product Information. Votrient (pazopanib)." GlaxoSmithKline
melatonin food
Applies to: elderberry / melatonin
MONITOR: Oral caffeine may significantly increase the bioavailability of melatonin. The proposed mechanism is inhibition of CYP450 1A2 first-pass metabolism. After administration of melatonin 6 mg and caffeine 200 mg orally (approximately equivalent to 1 large cup of coffee) to 12 healthy subjects, the mean peak plasma concentration (Cmax) of melatonin increased by 137% and the area under the concentration-time curve (AUC) increased by 120%. The metabolic inhibition was greater in nonsmokers (n=6) than in smokers (n=6). The greatest effect was seen in subjects with the *1F/*1F genotype (n=7), whose melatonin Cmax increased by 202%. The half-life did not change significantly. The clinical significance of this interaction is unknown.
According to some authorities, alcohol may reduce the effect of melatonin on sleep. The mechanism of this interaction is not fully understood.
In addition, CYP450 1A2 inducers like cigarette smoking may reduce exogenous melatonin plasma levels. In a small clinical trial (n=8), habitual smokers had their melatonin plasma levels measured two times, each after a single oral dose of 25 mg of melatonin. They had smoked prior to the first measurement but had not smoked for 7 days prior to the second. Cigarette smoking significantly reduced melatonin plasma exposure (AUC) as compared to melatonin levels after 7 days of smoking abstinence (7.34 +/- 1.85 versus 21.07 +/- 7.28 nmol/L*h, respectively).
MANAGEMENT: Caution and monitoring are recommended if melatonin is used with inhibitors of CYP450 1A2 like caffeine or inducers of CYP450 1A2 like cigarette smoking. Consumption of alcohol should be avoided when taking melatonin.
References (3)
- Hartter S, Nordmark A, Rose DM, Bertilsson L, Tybring G, Laine K (2003) "Effects of caffeine intake on the pharmacokinetics of melatonin, a probe drug for CYP1A2 activity." Br J Clin Pharmacol, 56, p. 679-682
- Cerner Multum, Inc. "UK Summary of Product Characteristics."
- Ursing C, Bahr CV, Brismar K, Rojdmark S (2005) "Influence of cigarette smoking on melatonin levels in man" Eur J Clin Pharmacol, 61, p. 197-201
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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