Drug Interactions between Briviact and st. john's wort
This report displays the potential drug interactions for the following 2 drugs:
- Briviact (brivaracetam)
- st. john's wort
Interactions between your drugs
St. John's wort brivaracetam
Applies to: st. john's wort and Briviact (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adjustments as well as clinical and laboratory monitoring may be appropriate whenever a CYP450 inducer is added to or withdrawn from therapy.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 (3)
- Cerner Multum, Inc. "UK Summary of Product Characteristics."
- 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
- (2016) "Product Information. Briviact (brivaracetam)." UCB Pharma Inc
Drug and food interactions
St. John's wort food
Applies to: st. john's wort
GENERALLY AVOID: An isolated case report suggests that foods containing large amounts of tyramine may precipitate a hypertensive crisis in patients treated with St. John's wort. The mechanism of interaction is unknown, as St. John's wort is not thought to possess monoamine oxidase (MAO) inhibiting activity at concentrations achieved in vivo. The case patient was a 41-year-old man who had been taking St. John's wort for seven days prior to presentation at the emergency room with confusion and disorientation. The patient recalled last eating aged cheese and having a glass of red wine approximately 10 hours prior to admission. No other cause of delirium or hypertension could be identified. In addition, alcohol may potentiate some of the pharmacologic effects of St. John's wort. Use in combination may result in additive central nervous system depression and/or impairment of judgment, thinking, and psychomotor skills.
MANAGEMENT: Until further information is available, patients treated with St. John's wort should consider avoiding consumption of protein foods in which aging or breakdown of protein is used to increase flavor. These foods include cheese (particularly strong, aged or processed cheeses), sour cream, wine (particularly red wine), champagne, beer, pickled herring, anchovies, caviar, shrimp paste, liver (particularly chicken liver), dry sausage, figs, raisins, bananas, avocados, chocolate, soy sauce, bean curd, yogurt, papaya products, meat tenderizers, fava beans, protein extracts, and dietary supplements. Caffeine may also precipitate hypertensive crisis so its intake should be minimized as well. Patients should also be advised to avoid or limit consumption of alcohol.
References (1)
- Patel S, Robinson R, Burk M (2002) "Hypertensive crisis associated with St. John's Wort." Am J Med, 112, p. 507-8
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.
See also
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. |
Further information
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