Drug Interaction Report
2 potential interactions and/or warnings found for the following 2 drugs:
- tacrine
- Trelegy Ellipta (fluticasone / umeclidinium / vilanterol)
Interactions between your drugs
tacrine vilanterol
Applies to: tacrine, Trelegy Ellipta (fluticasone / umeclidinium / vilanterol)
Tacrine can occasionally cause slowing of the heart rate or other irregular heart rhythm, and combining it with medications like vilanterol may increase that risk. Talk to your doctor if you have any questions or concerns. Your doctor may be able to prescribe alternatives that do not interact, or you may need a dose adjustment or more frequent monitoring to safely use both medications. Contact your doctor if you develop dizziness, lightheadedness, fainting, shortness of breath, chest pain, or heart palpitations during treatment. It is important to tell your doctor about all other medications you use, including vitamins and herbs. Do not stop using any medications without first talking to your doctor.
fluticasone vilanterol
Applies to: Trelegy Ellipta (fluticasone / umeclidinium / vilanterol), Trelegy Ellipta (fluticasone / umeclidinium / vilanterol)
Information for this minor interaction is available on the professional version.
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.
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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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