Drug Interactions between arimoclomol and Pronestyl
This report displays the potential drug interactions for the following 2 drugs:
- arimoclomol
- Pronestyl (procainamide)
Interactions between your drugs
procainamide arimoclomol
Applies to: Pronestyl (procainamide) 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
procainamide food
Applies to: Pronestyl (procainamide)
Ethanol may increase the acetylation of procainamide. Subtherapeutic plasma levels of procainamide may result in some patients. Because the acetylated metabolite of procainamide also possesses antiarrhythmic properties, the clinical effects are unclear.
References (1)
- Olsen H, Morland J (1982) "Ethanol-induced increase in procainamide acetylation in man." Br J Clin Pharmacol, 13, p. 203-8
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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