Drug Interactions between arimoclomol and guanfacine
This report displays the potential drug interactions for the following 2 drugs:
- arimoclomol
- guanfacine
Interactions between your drugs
guanFACINE arimoclomol
Applies to: guanfacine and arimoclomol
MONITOR: Arimoclomol may increase the systemic exposure and effects of organic cation transporter 2 (OCT2) substrates via inhibition of this renal uptake transporter. Clinical trials of arimoclomol done in patients with Niemann-Pick disease type C (NPC), healthy subjects, and patients with other diseases have observed mean increases in the endogenous substrate creatinine of 10% to 20% compared to baseline. One study in healthy male subjects (n=16) who received arimoclomol (744 mg/day for 28 days) observed a reversible increase in the mean serum creatinine of 19% after 21 days of treatment, without any effects on glomerular function. These increases may be due to inhibition of renal tubular secretion transporters.
MANAGEMENT: Caution and clinical monitoring are advised if arimoclomol is used in combination with an organic cation transporter 2 (OCT2) substrate. The labeling of the substrate should be consulted for specific monitoring, dose adjustment, and discontinuation recommendations should adverse reactions result from this combination. A reduction in the dose of the substrate may be necessary.
References (1)
- (2024) "Product Information. Miplyffa (arimoclomol)." Zevra Therapeutics, Inc.
Drug and food interactions
guanFACINE food
Applies to: guanfacine
GENERALLY AVOID: Grapefruit juice may increase the plasma concentrations of guanfacine. The risk of adverse reactions such as hypotension, bradycardia, and sedation may increase. The proposed mechanism is inhibition of CYP450 3A4-mediated first-pass metabolism in the gut wall by certain compounds present in grapefruit. Ketoconazole, a potent CYP450 3A4 inhibitor, has been reported to increase guanfacine peak plasma concentration (Cmax) and systemic exposure (AUC) by approximately 2- and 3-fold, respectively. A computer simulation suggests that fluconazole, a moderate CYP450 3A4 inhibitor, would increase guanfacine Cmax and AUC by about 1.5- and 2-fold, respectively. 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.
GENERALLY AVOID: Alcohol may enhance the sedative and hypotensive effects of guanfacine.
GENERALLY AVOID: Administration of extended-release guanfacine with a high-fat meal may increase the bioavailability of guanfacine. When a single 4 mg dose of extended-release guanfacine was administered to adult volunteers with a high-fat breakfast, mean guanfacine peak plasma concentration (Cmax) and systemic exposure (AUC) increased by approximately 75% and 40%, respectively, compared to dosing in a fasted state.
MANAGEMENT: Patients treated with guanfacine should avoid consumption of grapefruit and grapefruit juice. In addition, it is preferable to avoid or limit the use of alcohol during treatment. Patients should be advised against driving or operating hazardous machinery until they know how the medication affects them. The extended-release formulation of guanfacine should not be taken together with a high-fat meal.
References (3)
- (2001) "Product Information. Tenex (guanfacine)." Wyeth-Ayerst Laboratories
- Cerner Multum, Inc. "UK Summary of Product Characteristics."
- (2009) "Product Information. Intuniv (guanfacine)." Shire US Inc
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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