Drug Interactions between lecanemab and Normiflo
This report displays the potential drug interactions for the following 2 drugs:
- lecanemab
- Normiflo (ardeparin)
Interactions between your drugs
ardeparin lecanemab
Applies to: Normiflo (ardeparin) and lecanemab
MONITOR CLOSELY: Coadministration with drugs that can affect hemostasis such as glycoprotein IIb/IIIa inhibitors, thienopyridine antiplatelet agents, unfractionated and low molecular weight heparins, heparin derivatives, hirudin derivatives and analogs, thrombolytics, vitamin K antagonists, factor Xa inhibitors and other anticoagulants may potentiate the risk of bleeding complications associated with the use of the amyloid beta-directed antibody, lecanemab. Lecanemab therapy has been associated with amyloid related imaging abnormalities (ARIA) with hemosiderin deposition (ARIA-H), including microhemorrhage, superficial siderosis, and intracerebral hemorrhage, including fatal events. According to limited clinical trial data, concomitant use of lecanemab with aspirin, other antiplatelets (e.g., clopidogrel), or anticoagulants (e.g., dabigatran or warfarin) did not lead to an increased risk of ARIA-H compared to placebo; however, the majority of patients who received lecanemab were exposed to aspirin only so no definitive conclusions are possible. In addition, patients with known risk factors for intracerebral hemorrhage were excluded from clinical trials.
MANAGEMENT: Due to the risk of intracerebral hemorrhage, caution and close monitoring are recommended with the use of anticoagulants, antiplatelets, antithrombotics, or thrombolytic agents in patients already being treated with lecanemab, particularly those with risk factors for intracerebral hemorrhage.
References
- (2023) "Product Information. Leqembi (lecanemab)." Eisai Inc, 1
Drug and food interactions
No alcohol/food interactions were found. However, this does not necessarily mean no interactions exist. Always consult your healthcare provider.
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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