Drug Interaction Report
1 potential interaction and/or warning found for the following 2 drugs:
- edoxaban
- oritavancin
Interactions between your drugs
oritavancin edoxaban
Applies to: oritavancin, edoxaban
MONITOR CLOSELY: Use of oritavancin may interfere with the therapeutic monitoring of anticoagulants that depend on commonly used laboratory coagulation tests, as oritavancin can bind to and prevent the action of the tests' phospholipid reagents used to activate coagulation. Administration of oritavancin has been shown to artificially prolong the activated partial thromboplastin time (aPTT) for up to 120 hours and activated clotting time (ACT) for up to 24 hours following a single 1200 mg dose. Oritavancin my also artificially prolong the prothrombin time (PT) and international normalized ratio (INR) for up to 12 hours. However, studies indicate that oritavancin does not interfere with coagulation in vivo.
MANAGEMENT: For patients who require monitoring of anticoagulation within the indicated time after oritavancin dosing (e.g., aPTT less than or equal to 120 hrs, ACT less than or equal to 24 hrs, PT/INR less than or equal to 12 hrs), a non-phospholipid dependent coagulation test such as a Factor Xa (chromogenic) assay, or an alternative anticoagulant whose monitoring is not dependent on one of the affected tests may be considered.
References (3)
- (2024) "Product Information. Tenkasi (oritavancin)." A. Menarini Farmaceutica Internazionale SRL
- (2021) "Product Information. Kimyrsa (oritavancin)." Melinta Therapeutics, Inc.
- Dunois C (2021) "Laboratory Monitoring of Direct Oral Anticoagulants (DOACs)" Biomedicine, 9, p. 445
Drug and food interactions
No alcohol/food interactions were found with the drugs in your list. However, this does not necessarily mean no food interactions exist. Always consult your healthcare provider.
Therapeutic duplication warnings
No duplication 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
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. |
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Further information
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