Drug Interactions between Orkambi and Trikafta
This report displays the potential drug interactions for the following 2 drugs:
- Orkambi (ivacaftor/lumacaftor)
- Trikafta (elexacaftor/ivacaftor/tezacaftor)
Interactions between your drugs
lumacaftor tezacaftor
Applies to: Orkambi (ivacaftor / lumacaftor) and Trikafta (elexacaftor / ivacaftor / tezacaftor)
Consumer information for this interaction is not currently available.
GENERALLY AVOID: Coadministration with potent or moderate inducers of CYP450 3A4 may significantly decrease the plasma concentrations of vanzacaftor, tezacaftor, and deutivacaftor, drugs primarily metabolized by the isoenzyme. Physiologically based pharmacokinetic (PBPK) simulations suggest that coadministration with the potent CYP450 3A4 inducer rifampin may decrease vanzacaftor peak plasma concentration (Cmax) and systemic exposure (AUC) by 78% and 82%, respectively, and may decrease deutivacaftor Cmax and AUC by 80% and 90%, respectively. Similarly, the moderate CYP450 3A4 inducer efavirenz is predicted to decrease vanzacaftor Cmax and AUC by 65% and 69%, respectively; and may decrease deutivacaftor Cmax and AUC by 56% and 73%, respectively. No pharmacokinetic data are available for tezacaftor, but decreased exposures are expected according to prescribing information.
MANAGEMENT: Concomitant use of vanzacaftor, tezacaftor, and deutivacaftor containing medications with potent CYP450 3A4 inducers is not recommended.
lumacaftor elexacaftor
Applies to: Orkambi (ivacaftor / lumacaftor) and Trikafta (elexacaftor / ivacaftor / tezacaftor)
Consumer information for this interaction is not currently available.
GENERALLY AVOID: Coadministration with lumacaftor may decrease the plasma concentrations and therapeutic efficacy of drugs that are substrates of CYP450 3A4. Lumacaftor is a potent CYP450 3A4 inducer in vivo. Coadministration of lumacaftor with ivacaftor, a sensitive CYP450 3A4 substrate, decreased ivacaftor systemic exposure (AUC) by approximately 80%.
MANAGEMENT: Concomitant use of lumacaftor is not recommended with sensitive CYP450 3A4 substrates (e.g., oral midazolam, triazolam, lovastatin, simvastatin) or CYP450 3A4 substrates with a narrow therapeutic index (e.g., immunosuppressants such as cyclosporine, everolimus, sirolimus, and tacrolimus). Lumacaftor should also be avoided in patients receiving certain antibiotics (e.g., clarithromycin, erythromycin, telithromycin) and azole antifungal agents (e.g., itraconazole, ketoconazole, posaconazole, voriconazole). Alternatives to these agents should be considered. Some authorities recommend avoiding coadministration of lumacaftor-ivacaftor and itraconazole from 2 weeks before, during and for 2 weeks after treatment with itraconazole.
Drug and food interactions
ivacaftor food
Applies to: Orkambi (ivacaftor / lumacaftor) and Trikafta (elexacaftor / ivacaftor / tezacaftor)
Ivacaftor should be taken with fat-containing foods such as eggs, avocados, nuts, meat, butter, peanut butter, cheese pizza, and whole-milk dairy products to help with its absorption. Do not consume grapefruit juice or any food that contains grapefruit or Seville oranges during treatment with ivacaftor unless directed otherwise by your doctor. Grapefruit juice can significantly increase the blood levels of ivacaftor. This may increase the risk and/or severity of serious side effects such as liver damage. Call your doctor immediately if you have fever, chills, joint pain or swelling, unusual bleeding or bruising, skin rash, itching, loss of appetite, fatigue, nausea, vomiting, abdominal pain, dark urine, pale stools, and/or yellowing of the skin or eyes, as these may be signs and symptoms of liver damage. 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.
tezacaftor food
Applies to: Trikafta (elexacaftor / ivacaftor / tezacaftor)
Consumer information for this interaction is not currently available.
GENERALLY AVOID: Grapefruit juice may increase the plasma concentrations of tezacaftor, deutivacaftor, and vanzacaftor. The proposed mechanism is inhibition of CYP450 3A4-mediated first-pass metabolism in the gut wall by certain compounds present in grapefruit. In general, the effect of grapefruit juice is concentration-, dose- and preparation- dependent, and can vary widely among brands. Certain preparations of grapefruit juice (e.g., high dose, double strength) have sometimes demonstrated potent inhibition of CYP450 3A4, while other preparations (e.g., low dose, single strength) have typically demonstrated moderate inhibition. The risk and/or severity of serious side effects such as liver damage may be increased.
ADJUST DOSING INTERVAL: Administration with fat-containing food may increase the oral bioavailability of vanzacaftor and deutivacaftor. Administration with a fat containing meal increased vanzacaftor systemic exposure (AUC) by 4- (low-fat meal) to 6- (high-fat meal) fold. While deutivacaftor AUC increased approximately 3- (low-fat meal) to 4- (high-fat meal) fold, relative to administration in a fasting state. Tezacaftor exposure is not significantly affected by administration of fat-containing foods.
MANAGEMENT: Patients treated with tezacaftor, deutivacaftor, vanzacaftor -containing medications should avoid consumption of grapefruit juice and any food that contains grapefruit. To improve absorption, patients should be advised to take vanzacaftor and/or deutivacaftor containing medications with fat-containing foods such as eggs, avocados, nuts, meat, butter, peanut butter, cheese pizza, and whole-milk dairy products at approximately the same time of the day. A typical cystic fibrosis diet will satisfy this requirement.
Therapeutic duplication warnings
Therapeutic duplication is the use of more than one medicine from the same drug category or therapeutic class to treat the same condition. This can be intentional in cases where drugs with similar actions are used together for demonstrated therapeutic benefit. It can also be unintentional in cases where a patient has been treated by more than one doctor, or had prescriptions filled at more than one pharmacy, and can have potentially adverse consequences.
Cftr modulators
Therapeutic duplication
The recommended maximum number of medicines in the 'CFTR modulators' category to be taken concurrently is usually one. Your list includes two medicines belonging to the 'CFTR modulators' category:
- Orkambi (ivacaftor/lumacaftor)
- Trikafta (elexacaftor/ivacaftor/tezacaftor)
Note: In certain circumstances, the benefits of taking this combination of drugs may outweigh any risks. Always consult your healthcare provider before making changes to your medications or dosage.
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
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
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