Drug Interactions between encorafenib and Soltamox
This report displays the potential drug interactions for the following 2 drugs:
- encorafenib
- Soltamox (tamoxifen)
Interactions between your drugs
tamoxifen encorafenib
Applies to: Soltamox (tamoxifen) and encorafenib
Consumer information for this interaction is not currently available.
GENERALLY AVOID: Coadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of tamoxifen, which is metabolized by the isoenzyme. In ten healthy subjects, the potent CYP450 3A4 inducer rifampin (600 mg orally once a day for 5 days) decreased the peak plasma concentration (Cmax), area under the concentration-time curve (AUC) and elimination half-life of tamoxifen (80 mg single oral dose) by 55%, 86% and 44%, respectively, compared to placebo. The AUC of the active N-demethyl metabolite decreased by 62% and Cmax increased by 46%, suggesting enhanced presystemic metabolism in the intestine. Aminoglutethimide has also been reported to significantly increase the clearance of tamoxifen by more than 3-fold. Coadministration of another CYP450 3A4 inducer, bexarotene, resulted in a 35% decrease in plasma concentrations of tamoxifen. The extent to which other CYP450 3A4 inducers may affect tamoxifen is unknown.
MANAGEMENT: In general, agents without CYP450 3A4-inducing activity are preferable in patients treated with tamoxifen, particularly if these agents are to be used for a prolonged period. Otherwise, pharmacologic response to tamoxifen should be monitored closely whenever an inducing agent is added to or withdrawn from therapy, and the tamoxifen dosage adjusted if necessary.
References
- Lien EA, Anker G, Lonning PE, et al. (1990) "Decreased serum concentrations of tamoxifen and its metabolites induced by aminoglutethimide." Cancer Res, 50, p. 5851-7
- Kivisto KT, Villikka K, Nyman L, Anttila M, Neuvonen PJ (1998) "Tamoxifen and toremifene concentrations in plasma are greatly decreased by rifampin." Clin Pharmacol Ther, 64, p. 648-54
- (2001) "Product Information. Targretin (bexarotene)." Ligand Pharmaceuticals
- Biochem Pharmacol (1997) "Variable contribution of cytochromes P450 2D6, 2C9, and 3A4 to the 4-hydroxylation of tamoxifen by human liver microsomes." Biochem Pharmacol, 53, p. 171-8
Drug and food interactions
encorafenib food
Applies to: encorafenib
You should preferably avoid consumption of grapefruit and grapefruit juice while taking encorafenib. Grapefruit and grapefruit juice can significantly increase the blood levels of encorafenib. This may increase the risk of serious side effects such as bleeding complications, eye and vision problems, liver problems, irregular heart rhythm, and development of new skin cancers. Talk to your doctor if you have any questions or concerns. It is important to tell your doctor about all other medications you use, including vitamins and herbs. Do not stop using any medications without first talking to your doctor.
tamoxifen food
Applies to: Soltamox (tamoxifen)
Talk to your doctor before using tamoxifen with soy products. There is some evidence that substances present in soy may stimulate breast tumor growth and interfere with the action of tamoxifen, although this has not been proven. Whether soy products are effective for hot flashes is also uncertain. It is important to tell your doctor about all other medications you use, including vitamins and herbs. Do not stop using any medications without first talking to your doctor.
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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