Drug Interactions between azithromycin and Prograf
This report displays the potential drug interactions for the following 2 drugs:
- azithromycin
- Prograf (tacrolimus)
Interactions between your drugs
azithromycin tacrolimus
Applies to: azithromycin and Prograf (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)
- (2002) "Product Information. Zithromax (azithromycin)." Pfizer U.S. Pharmaceuticals
- Ibrahim RB, Abella EM, Chandrasekar PH (2002) "Tacrolimus-clarithromycin interaction in a patient receiving bone marrow transplantation." Ann Pharmacother, 36, p. 1971-1972
- 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
- 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 interactions
tacrolimus food
Applies to: Prograf (tacrolimus)
ADJUST DOSING INTERVAL: Consumption of food has led to a 27% decrease in the bioavailability of orally administered tacrolimus.
MANAGEMENT: Tacrolimus should be administered at least one hour before or two hours after meals.
GENERALLY AVOID: Grapefruit juice has been reported to increase tacrolimus trough concentrations. Data are limited, but inhibition of the CYP450 enzyme system appears to be involved.
MANAGEMENT: The clinician may want to recommend that the patient avoid ingesting large amounts of grapefruit juice while taking tacrolimus.
References (2)
- (2001) "Product Information. Prograf (tacrolimus)." Fujisawa
- Hooks MA (1994) "Tacrolimus, a new immunosuppressant--a review of the literature." Ann Pharmacother, 28, p. 501-11
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
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