Drug Interaction Report
1 potential interaction and/or warning found for the following 2 drugs:
- NovoSeven RT (coagulation factor viia)
- ticagrelor
Interactions between your drugs
coagulation factor VIIa ticagrelor
Applies to: NovoSeven RT (coagulation factor viia), ticagrelor
Antifibrinolytic agents (e.g., aminocaproic acid or tranexamic acid) and recombinant factor VIIa may increase hemostasis and antagonize the effects of ticagrelor. They may be more effective in managing clinical bleeding events that occur during ticagrelor therapy compared to platelet infusions or desmopressin. No data exist regarding a hemostatic benefit of platelet transfusions in the presence of ticagrelor; circulating ticagrelor may inhibit transfused platelets. Template bleeding time did not decrease when ticagrelor was coadministered with desmopressin; therefore, desmopressin is unlikely to be effective in managing clinical bleeding events. Ticagrelor should be discontinued if active bleeding occurs, and may be resumed after the bleeding has been controlled and the cause identified.
References (2)
- Cerner Multum, Inc. "UK Summary of Product Characteristics."
- (2011) "Product Information. Brilinta (ticagrelor)." Astra-Zeneca Pharmaceuticals
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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