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Drug Interactions between brivaracetam and Luminal

This report displays the potential drug interactions for the following 2 drugs:

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Interactions between your drugs

Moderate

PHENobarbital brivaracetam

Applies to: Luminal (phenobarbital) and brivaracetam

MONITOR: Coadministration with potent inducers of CYP450 isoenzymes may decrease the plasma concentrations of brivaracetam, which is partially metabolized by CYP450 2C19. In healthy study subjects, administration of brivaracetam with the potent CYP450 inducer rifampin (600 mg/day for 5 days) resulted in a 45% decrease in brivaracetam systemic exposure (AUC). When given with the enzyme-inducing antiepileptic drugs carbamazepine, phenytoin and phenobarbital, the AUC of brivaracetam decreased by 26%, 21%, and 19%, respectively, without significant effects on pharmacologic response based on a population pharmacokinetic/pharmacodynamic analysis of placebo-controlled phase 3 studies. Conversely, concomitant use of phenytoin with a supratherapeutic dose of brivaracetam (400 mg/day) resulted in a 20% increase in phenytoin peak plasma concentration (Cmax) and AUC. Following administration of carbamazepine with brivaracetam dosages of 50 mg/day, 100 mg/day and 200 mg/day, no significant pharmacokinetic changes were observed for carbamazepine, but the plasma concentrations of carbamazepine epoxide (an active metabolite associated with neurotoxicity) increased by a mean of 37%, 62% and 98%, respectively. Coadministration of brivaracetam 200 mg twice daily and carbamazepine 300 mg twice daily for two weeks increased the AUC of carbamazepine epoxide by approximately 160% in 13 healthy male subjects. No safety risks were observed with these increases. Brivaracetam is a moderate reversible inhibitor of epoxide hydrolase, the enzyme that catalyzes the hydrolysis of carbamazepine epoxide to an inactive metabolite.

MANAGEMENT: The potential for diminished pharmacologic effects of brivaracetam should be considered during coadministration with potent CYP450 enzyme inducers. Dosage adjustments as well as clinical and laboratory monitoring may be appropriate whenever a CYP450 inducer is added to or withdrawn from therapy. For patients receiving concomitant carbamazepine or phenytoin therapy, blood levels should be monitored following initiation or discontinuation of brivaracetam. Dosage reductions for carbamazepine and phenytoin may be required if tolerability issues arise.

References

  1. Cerner Multum, Inc. "UK Summary of Product Characteristics."
  2. Stockis A, Chanteux H, Rosa M, Rolan P (2015) "Brivaracetam and carbamazepine interaction in healthy subjects and in vitro." Epilepsy Res, 113, p. 19-27
  3. (2016) "Product Information. Briviact (brivaracetam)." UCB Pharma Inc

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Drug and food interactions

Major

PHENobarbital food

Applies to: Luminal (phenobarbital)

GENERALLY AVOID: Concurrent acute use of barbiturates and ethanol may result in additive CNS effects, including impaired coordination, sedation, and death. Tolerance of these agents may occur with chronic use. The mechanism is related to inhibition of microsomal enzymes acutely and induction of hepatic microsomal enzymes chronically.

MANAGEMENT: The combination of ethanol and barbiturates should be avoided.

References

  1. Gupta RC, Kofoed J (1966) "Toxological statistics for barbiturates, other sedatives, and tranquilizers in Ontario: a 10-year survey." Can Med Assoc J, 94, p. 863-5
  2. Misra PS, Lefevre A, Ishii H, Rubin E, Lieber CS (1971) "Increase of ethanol, meprobamate and pentobarbital metabolism after chronic ethanol administration in man and in rats." Am J Med, 51, p. 346-51
  3. Saario I, Linnoila M (1976) "Effect of subacute treatment with hypnotics, alone or in combination with alcohol, on psychomotor skills related to driving." Acta Pharmacol Toxicol (Copenh), 38, p. 382-92
  4. Stead AH, Moffat AC (1983) "Quantification of the interaction between barbiturates and alcohol and interpretation of fatal blood concentrations." Hum Toxicol, 2, p. 5-14
  5. Seixas FA (1979) "Drug/alcohol interactions: avert potential dangers." Geriatrics, 34, p. 89-102
View all 5 references

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Therapeutic duplication warnings

No 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

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.