What are the interactions of Ticlopidine (Tikosen)?

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Last updated: April 16, 2025View editorial policy

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From the Guidelines

Tikosen is not a recognized medication, and thus, its interactions cannot be definitively determined, but if referring to ticlopidine, it should be used with caution, especially with medications like aspirin, warfarin, and ibuprofen, due to potential interactions and side effects 1.

When considering the management of patients with unstable angina or non-ST-elevation myocardial infarction (UA/NSTEMI), the use of antiplatelet and anticoagulant therapies is crucial. For patients allergic to clopidogrel, ticlopidine is an alternative, dosed at 250 mg orally twice daily 1. However, the interaction between ticlopidine and other medications, such as aspirin and warfarin, must be carefully managed to minimize the risk of bleeding complications.

Key considerations include:

  • The concomitant use of aspirin and ticlopidine may increase the risk of bleeding, and thus, monitoring is essential.
  • Warfarin, when added to aspirin and another antiplatelet agent like ticlopidine, requires careful adjustment to maintain an INR between 2.0 and 2.5 to balance the risk of thrombosis and bleeding 1.
  • Nonsteroidal anti-inflammatory drugs (NSAIDs) like ibuprofen can interact with aspirin, potentially reducing its efficacy, and should be used with caution or alternative NSAIDs considered 1.

Given the potential for significant interactions and the importance of minimizing morbidity, mortality, and improving quality of life, it is crucial for patients to be closely monitored by their healthcare provider when on ticlopidine or any other antithrombotic regimen, especially if there are concerns about drug interactions or side effects 1.

From the Research

Tikosen Interactions

There are no direct mentions of Tikosen interactions in the provided studies. However, the studies discuss general drug-drug interactions and their mechanisms:

  • Drug-drug interactions (DDIs) can occur through pharmacodynamic or pharmacokinetic interactions, affecting the absorption, distribution, metabolism, or excretion of another drug 2.
  • Common DDIs result from alterations in drug metabolism through interactions with cytochrome P450 enzymes and absorption through interactions with P-glycoproteins 2.
  • Additive effects, such as combinations of drugs that increase the risk of seizures, prolong the QT interval, increase central nervous system depression, and increase the risk of serotonin syndrome, are also common 2.
  • Strategies for reducing the risk of drug-drug interactions include minimizing the number of drugs prescribed, re-evaluating therapy on a regular basis, and considering nonpharmacologic options 3.

Mechanisms of Drug Interactions

Some studies discuss specific mechanisms of drug interactions:

  • Inhibition or induction of cytochrome P450 drug metabolizing isoenzymes is the most common mechanism by which clinically important drug interactions occur 3.
  • The antimicrobials most likely to affect the international normalized ratio significantly in patients receiving warfarin are trimethoprim/sulfamethoxazole, metronidazole, and fluconazole 3.

Management of Drug Interactions

The studies also discuss the management of drug interactions:

  • Drug-related clinical decision support has been shown to improve the quality of patient care and decrease adverse drug event rates 2.
  • Physicians should consider consultation with a clinical pharmacist when clinical circumstances require the use of drugs with interaction potential 3.
  • Prescription data may be useful in quality-improvement programmes to identify groups of patients and practices at increased risk of drug interactions 4.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Risk factors for potential drug interactions in general practice.

The European journal of general practice, 2008

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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