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Rufinamide Disease Interactions

There are 4 disease interactions with rufinamide.

Major

Anticonvulsants (applies to rufinamide) depression

Major Potential Hazard, Moderate plausibility.

Antiepileptic drugs can increase depression and suicidal thoughts or behaviors in patients receiving these drugs for any indication. Patients should be monitored for the emergence or worsening of depression, suicidal thoughts and unusual changes in mood or behavior. Caregivers and family should be alert for the emergence or worsening of symptoms. Behaviors of concern should be reported immediately to the healthcare providers.

References

  1. (2002) "Product Information. Tegretol (carbamazepine)." Novartis Pharmaceuticals
  2. (2001) "Product Information. Depakene (valproic acid)." Abbott Pharmaceutical
  3. (2001) "Product Information. Depakote (divalproex sodium)." Abbott Pharmaceutical
  4. (2001) "Product Information. Lamictal (lamotrigine)." Glaxo Wellcome
  5. (2001) "Product Information. Magnesium Sulfate (magnesium sulfate)." Abbott Pharmaceutical
  6. (2001) "Product Information. Trileptal (oxcarbazepine)." Novartis Pharmaceuticals
  7. (2008) "Product Information. Vimpat (lacosamide)." UCB Pharma Inc
  8. (2008) "Product Information. Banzel (rufinamide)." Eisai Inc
  9. (2013) "Product Information. Aptiom (eslicarbazepine)." Sunovion Pharmaceuticals Inc
View all 9 references
Major

Anticonvulsants (applies to rufinamide) liver disease

Major Potential Hazard, Moderate plausibility.

Most anticonvulsants are primarily metabolized by the liver. Metabolic activity may be decreased in patients with liver disease, resulting in elevated drug levels and increased risk of toxicity. Therapy with anticonvulsants should be administered cautiously in patients with mild and moderate liver impairment. Therapy with these drugs is mostly not recommended in patients with severe liver impairment. Caution is also advised when treating patients with a history of liver disease, since the use of some anticonvulsants has been associated with hepatotoxicity. Baseline and periodic evaluation of liver function is recommended. Therapy should be discontinued and not readministered if evidence of liver damage is observed and felt to be drug-related.

References

  1. (2002) "Product Information. Tegretol (carbamazepine)." Novartis Pharmaceuticals
  2. (2008) "Product Information. Banzel (rufinamide)." Eisai Inc
  3. (2013) "Product Information. Aptiom (eslicarbazepine)." Sunovion Pharmaceuticals Inc
  4. (2014) "Product Information. Oxtellar XR (oxcarbazepine)." Supernus Pharmaceuticals Inc
View all 4 references
Major

Anticonvulsants (applies to rufinamide) renal dysfunction

Major Potential Hazard, Moderate plausibility.

Most anticonvulsants are primarily excreted by the kidney. The plasma clearance may be decreased and the half-life prolonged in patients with impaired renal function. Therapy with anticonvulsants should be administered cautiously in patients with significant renal dysfunction. In most cases it is recommended to adjust the dosage in patients with CrCl <50 mL/min to half the usual starting dose and then increase slowly to achieve the desired clinical response. The renal function should be monitored regularly in patients receiving therapy.

References

  1. (2002) "Product Information. Tegretol (carbamazepine)." Novartis Pharmaceuticals
  2. (2001) "Product Information. Trileptal (oxcarbazepine)." Novartis Pharmaceuticals
  3. (2008) "Product Information. Banzel (rufinamide)." Eisai Inc
  4. (2013) "Product Information. Aptiom (eslicarbazepine)." Sunovion Pharmaceuticals Inc
View all 4 references
Major

Rufinamide (applies to rufinamide) short QT syndrome

Major Potential Hazard, Moderate plausibility.

Rufinamide can cause shortening of the QT interval. Its use is contraindicated in patients with Familial Short QT syndrome as this condition is associated with increased risk of sudden death and ventricular arrhythmias, particularly ventricular fibrillation.

References

  1. (2008) "Product Information. Banzel (rufinamide)." Eisai Inc

Rufinamide drug interactions

There are 492 drug interactions with rufinamide.

Rufinamide alcohol/food interactions

There is 1 alcohol/food interaction with rufinamide.


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Drug Interaction Classification

These classifications are only a guideline. The relevance of a particular drug interaction to a specific individual is difficult to determine. Always consult your healthcare provider before starting or stopping any medication.
Major Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit.
Moderate Moderately clinically significant. Usually avoid combinations; use it only under special circumstances.
Minor 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.
Unknown No interaction information available.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.