Drug Interactions between dexamethasone and lorlatinib
This report displays the potential drug interactions for the following 2 drugs:
- dexamethasone
- lorlatinib
Interactions between your drugs
dexAMETHasone lorlatinib
Applies to: dexamethasone and lorlatinib
GENERALLY AVOID: Coadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of lorlatinib, which may decrease its efficacy. In vitro studies have shown lorlatinib is metabolized primarily by CYP450 3A4 and UGT1A4. When a single 100 mg oral dose of lorlatinib was administered to subjects receiving modafinil, a moderate CYP450 3A4 inducer, mean lorlatinib peak plasma concentration (Cmax) and systemic exposure (AUC) decreased by 22% and 23%, respectively. Strong CYP450 3A inducers are contraindicated for use with lorlatinib due to risk of serious hepatotoxicity. No clinically meaningful changes in liver function tests were seen in healthy subjects after receiving a combination of lorlatinib with the moderate CYP450 3A4/5 inducer modafinil (400 mg once a day for 19 days).
MANAGEMENT: Concomitant use of lorlatinib with moderate CYP450 3A4 inducers should generally be avoided. If coadministration is unavoidable, the lorlatinib dose should be increased from 100 mg once a day to 125 mg once a day.
References (1)
- (2018) "Product Information. Lorbrena (lorlatinib)." Pfizer U.S. Pharmaceuticals Group
Drug and food interactions
lorlatinib food
Applies to: lorlatinib
GENERALLY AVOID: Grapefruit and grapefruit juice may significantly increase the plasma concentrations of lorlatinib. The proposed mechanism is inhibition of CYP450 3A4-mediated first-pass metabolism in the gut wall induced by certain compounds present in grapefruit. Because grapefruit juice inhibits primarily intestinal rather than hepatic CYP450 3A4, the magnitude of interaction is greatest for those drugs that undergo significant presystemic metabolism by CYP450 3A4 (i.e., drugs with low oral bioavailability). In general, the effect of grapefruit juice is concentration-, dose- and preparation-dependent, and can vary widely among brands. Certain preparations of grapefruit juice (e.g., high dose, double strength) have sometimes demonstrated potent inhibition of CYP450 3A4, while other preparations (e.g., low dose, single strength) have typically demonstrated moderate inhibition. Pharmacokinetic interactions involving grapefruit juice are also subject to a high degree of interpatient variability, thus the extent to which a given patient may be affected is difficult to predict.
MANAGEMENT: Patients treated with lorlatinib should avoid consumption of grapefruit, grapefruit juice, and any supplement containing grapefruit extract. If coadministration is unavoidable, some authorities recommend reducing the initial dosage of lorlatinib from 100 mg orally once daily to 75 mg orally once daily. In patients who have had a dosage reduction to 75 mg orally once daily due to adverse reactions, the lorlatinib dosage should be further reduced to 50 mg orally once daily upon initiation of a potent CYP450 3A4 inhibitor. After 3 plasma half-lives following discontinuation of the potent CYP450 3A4 inhibitor, the lorlatinib dosage may be increased to that used prior to initiation of the inhibitor.
References (2)
- Cerner Multum, Inc. "UK Summary of Product Characteristics."
- (2018) "Product Information. Lorbrena (lorlatinib)." Pfizer U.S. Pharmaceuticals Group
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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