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Drug Interactions between azithromycin and Envarsus XR

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

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Interactions between your drugs

Moderate

azithromycin tacrolimus

Applies to: azithromycin and Envarsus XR (tacrolimus)

MONITOR: Both azithromycin and tacrolimus have rarely been associated with QT interval prolongation. Theoretically, concomitant use may result in additive effects and increased risk of ventricular arrhythmias including torsade de pointes and sudden death. In general, the risk of an individual agent or a combination of these agents causing ventricular arrhythmia in association with QT prolongation is largely unpredictable but may be increased by certain underlying risk factors such as congenital long QT syndrome, cardiac disease, and electrolyte disturbances (e.g., hypokalemia, hypomagnesemia). In addition, the extent of drug-induced QT prolongation is dependent on the particular drug(s) involved and dosage(s) of the drug(s).

MONITOR: Rarely, azithromycin has been reported to increase the plasma concentrations of tacrolimus. The exact mechanism has not been established, since azithromycin is not generally considered an inhibitor of CYP450 3A4 or P-glycoprotein, of which tacrolimus is a substrate. Supportive evidence is limited to two published case reports. In one report, a patient receiving intravenous tacrolimus had a twofold increase in his tacrolimus levels three days after the initiation of azithromycin 500 mg/day. In the other report, a heart transplant patient had increased tacrolimus blood levels following the administration of intravenous azithromycin and ceftriaxone. Tacrolimus levels decreased after the discontinuation of ceftriaxone and switch from intravenous to oral azithromycin. In contrast, a 10-day course of azithromycin reportedly had no significant effect on serum creatinine or tacrolimus levels in a bone marrow transplant patient treated with tacrolimus.

MANAGEMENT: Caution and clinical monitoring are recommended when azithromycin and tacrolimus are prescribed in combination. Patients should be advised to seek medical attention if they experience symptoms that could indicate the occurrence of torsade de pointes such as dizziness, lightheadedness, fainting, palpitations, irregular heartbeat, shortness of breath, or syncope. It may be appropriate to monitor tacrolimus levels more closely following the initiation or discontinuation of azithromycin.

References (4)
  1. (2002) "Product Information. Zithromax (azithromycin)." Pfizer U.S. Pharmaceuticals
  2. Ibrahim RB, Abella EM, Chandrasekar PH (2002) "Tacrolimus-clarithromycin interaction in a patient receiving bone marrow transplantation." Ann Pharmacother, 36, p. 1971-1972
  3. Mori T, Aisa Y, Nakazato T, Yamazaki R, Ikeda Y, Okamoto S (2005) "Tacrolimus-azithromycin interaction in a recipient of allogeneic bone marrow transplantation." Transpl Int, 18, p. 757-8
  4. Shullo MA, Schonder K, Teuteberg JJ (2010) "Elevated tacrolimus levels associated with intravenous azithromycin and ceftriaxone: a case report." Transplant Proc, 42, p. 1870-2

Drug and food/lifestyle interactions

Major

tacrolimus food/lifestyle

Applies to: Envarsus XR (tacrolimus)

GENERALLY AVOID: Grapefruit and/or grapefruit juice may increase the plasma concentrations of tacrolimus. The proposed mechanism for the interaction is inhibition of CYP450 3A4-mediated first-pass metabolism in the gut wall by certain compounds present in grapefruit. Inhibition of hepatic CYP450 3A4 may also contribute. Although clinical data are lacking, this interaction may result in increased risk of serious adverse reactions such as nephro- and neurotoxicity, as well as other adverse effects associated with tacrolimus such as malignancies, infections, diabetes, hyperkalemia, hypertension, and QT prolongation.

GENERALLY AVOID: Alcohol may modify the rate of tacrolimus release from extended release formulations, thereby potentially increasing the risk of serious adverse reactions.

ADJUST DOSING INTERVAL: Coadministration with food decreases the rate and extent of tacrolimus absorption. This effect is greatest after a high-fat meal.

MANAGEMENT: Patients should avoid consumption of food or drink containing grapefruit during treatment with tacrolimus. Concomitant use of tacrolimus, especially extended release formulations, with alcohol should also be avoided. Tacrolimus extended release formulations should be administered on an empty stomach, at least 1 hour before or 2 hours after a meal, and tacrolimus immediate release formulations should be taken consistently every day with or without food.

References (18)
  1. (2001) "Product Information. Prograf (tacrolimus)." Fujisawa
  2. Hooks MA (1994) "Tacrolimus, a new immunosuppressant--a review of the literature." Ann Pharmacother, 28, p. 501-11
  3. (2022) "Product Information. Adoport (tacrolimus)." Sandoz Ltd
  4. (2024) "Product Information. TACrolimus (Sandoz) (TACrolimus)." Sandoz Pty Ltd
  5. (2023) "Product Information. Prograf (tacrolimus)." Astellas Pharma US, Inc
  6. (2023) "Product Information. Astagraf XL (tacrolimus)." Astellas Pharma US, Inc
  7. (2025) "Product Information. Envarsus XR (tacrolimus)." Veloxis Pharmaceuticals
  8. (2024) "Product Information. Prograf (tacrolimus)." Astellas Pharma Canada Inc
  9. (2024) "Product Information. Advagraf (tacrolimus)." Astellas Pharma Canada Inc
  10. (2024) "Product Information. Envarsus PA (tacrolimus)." Endo Operations LTD
  11. (2024) "Product Information. Dailiport (tacrolimus)." Sandoz Ltd
  12. (2025) "Product Information. Prograf (tacrolimus)." Astellas Pharma Ltd
  13. (2025) "Product Information. Envarsus (tacrolimus)." Chiesi Ltd
  14. (2025) "Product Information. Advagraf (tacrolimus)." Astellas Pharma Ltd
  15. (2025) "Product Information. Modigraf (tacrolimus)." Astellas Pharma Ltd
  16. (2024) "Product Information. Advagraf XL (TACrolimus)." Astellas Pharma Australia Pty Ltd
  17. (2024) "Product Information. proGRAF (TACrolimus)." Astellas Pharma Australia Pty Ltd
  18. (2024) "Product Information. TACrolimus XR (Sandoz) (TACrolimus)." Sandoz Pty Ltd

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.


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.