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Drug Interactions between carbamazepine and etrasimod

This report displays the potential drug interactions for the following 2 drugs:

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Interactions between your drugs

Major

carBAMazepine etrasimod

Applies to: carbamazepine and etrasimod

GENERALLY AVOID: Coadministration with moderate to potent inducers of two or more of the isoenzymes CYP450 2C8, CYP450 2C9, or CYP450 3A4 may decrease the plasma concentrations of etrasimod, which is primarily metabolized by these isoenzymes. Reduced therapeutic efficacy of etrasimod may occur. In clinical drug interaction studies, concomitant use of etrasimod with rifampin, a combined strong inducer of CYP450 3A4 and moderate inducer of CYP450 2C8 and 2C9, decreased the systemic exposure (AUC) of etrasimod by 49%.

MANAGEMENT: Concomitant use of etrasimod with one or a combination of drugs that are moderate to strong inducers of at least two of the isoenzymes CYP450 2C8, CYP450 2C9, or CYP450 3A4, such as rifampin, is not recommended.

References (6)
  1. (2023) "Product Information. Velsipity (etrasimod)." Pfizer U.S. Pharmaceuticals Group
  2. (2024) "Product Information. Velsipity (etrasimod)." Pfizer Australia Pty Ltd, pfpvelst11024
  3. (2024) "Product Information. Velsipity (etrasimod)." Pfizer Ltd
  4. (2024) "Product Information. Velsipity (etrasimod)." Pfizer U.S. Pharmaceuticals Group
  5. (2024) "Product Information. Velsipity (etrasimod)." Pfizer Canada ULC
  6. Harnik S, Ungar B, Loebstein R, Ben-Horin S (2024) "A Gastroenterologist's guide to drug interactions of small molecules for inflammatory bowel disease" United European Gastroenterol J, 12, p. 627-637

Drug and food interactions

Moderate

carBAMazepine food

Applies to: carbamazepine

GENERALLY AVOID: Alcohol may potentiate some of the pharmacologic effects of carbamazepine. Use in combination may result in additive central nervous system depression and/or impairment of judgment, thinking, and psychomotor skills.

In a small, randomized, crossover study, the administration of carbamazepine with grapefruit juice (compared to water) increased plasma drug concentrations by approximately 40%. The proposed mechanism is inhibition of CYP450 3A4-mediated first-pass metabolism in the gut wall by certain compounds present in grapefruits.

MANAGEMENT: Patients receiving carbamazepine should be advised to avoid or limit consumption of alcohol. Given the drug's narrow therapeutic index, patients receiving carbamazepine therapy should preferably avoid the regular consumption of grapefruits and grapefruit juice to prevent any undue fluctuations in plasma drug levels. Patients should be advised to report signs of carbamazepine toxicity (nausea, visual disturbances, dizziness, or ataxia) to their physicians.

References (3)
  1. (2002) "Product Information. Tegretol (carbamazepine)." Novartis Pharmaceuticals
  2. Garg SK, Kumar N, Bhargava VK, Prabhakar SK (1998) "Effect of grapefruit juice on carbamazepine bioavailability in patients with epilepsy." Clin Pharmacol Ther, 64, p. 286-8
  3. Bailey DG, Dresser GR, Kreeft JH, Munoz C, Freeman DJ, Bend JR (2000) "Grapefruit-felodipine interaction: Effect of unprocessed fruit and probable active ingredients." Clin Pharmacol Ther, 68, p. 468-77
Moderate

etrasimod food

Applies to: etrasimod

GENERALLY AVOID: Coadministration with moderate inhibitors of CYP450 3A4 such as grapefruit juice in patients who known or suspected to be poor CYP450 2C9 metabolizers may increase the exposure of etrasimod. Etrasimod is primarily metabolized by the isoenzymes CYP450 3A4, 2C8, and 2C9. Pharmacokinetic studies have reported that no single enzyme system appears to dominate the elimination pathway of etrasimod. Therefore, the involvement of multiple CYP450 isoforms reduces the likelihood of drug-drug interactions when only a single CYP450 isoform is strongly or moderately inhibited by a coadministered drug. In clinical drug interaction studies, when etrasimod was administered with the dual moderate CYP450 2C9 and 3A4 inhibitor fluconazole at steady-state levels, etrasimod systemic exposure (AUC) increased by 84%. However, concomitant use with the potent CYP450 3A4 inhibitor itraconazole increased the AUC of etrasimod by 32%, which was not considered by the manufacturer to be clinically significant. The effect on etrasimod systemic exposure in CYP450 2C9 intermediate metabolizers treated with less potent CYP450 3A4 inhibitors is not known. Increased plasma concentrations of etrasimod may increase the risk of infection, bradyarrhythmia, AV conduction delays, elevated transaminase levels, and macular edema.

MANAGEMENT: Until further information is available, the consumption of grapefruit and grapefruit juice in combination with moderate to potent CYP450 2C8 inhibitors such as gemfibrozil should be avoided or limited during treatment with etrasimod in patients who are poor CYP450 2C9 metabolizers. Caution is recommended with grapefruit products consumption in patients who are intermediate CYP450 2C9 metabolizers. Patients should be advised to notify their physician if they experience potential adverse effects of etrasimod.

References (6)
  1. (2023) "Product Information. Velsipity (etrasimod)." Pfizer U.S. Pharmaceuticals Group
  2. Lee C, Taylor C, Tang Y, Caballero LV, shan k, Randle A, Grundy JS (2022) Effects of fluconazole, gemfibrozil, and rifampin on the pharmacokinetics, safety, and tolerability of etrasimod https://gut.bmj.com/content/71/Suppl_1/A142.1
  3. (2024) "Product Information. Velsipity (etrasimod)." Pfizer Australia Pty Ltd, pfpvelst11024
  4. (2024) "Product Information. Velsipity (etrasimod)." Pfizer U.S. Pharmaceuticals Group
  5. (2024) "Product Information. Velsipity (etrasimod)." Pfizer Canada ULC
  6. Harnik S, Ungar B, Loebstein R, Ben-Horin S (2024) "A Gastroenterologist's guide to drug interactions of small molecules for inflammatory bowel disease" United European Gastroenterol J, 12, p. 627-637

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.


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Drug Interaction Classification

These classifications are only a guideline. The relevance of a particular drug interaction to a specific individual is difficult to determine. Always consult your healthcare provider before starting or stopping any medication.
Major Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit.
Moderate Moderately clinically significant. Usually avoid combinations; use it only under special circumstances.
Minor 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.
Unknown No interaction information available.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.