Drug Interactions between Jaypirca and riociguat
This report displays the potential drug interactions for the following 2 drugs:
- Jaypirca (pirtobrutinib)
- riociguat
Interactions between your drugs
riociguat pirtobrutinib
Applies to: riociguat and Jaypirca (pirtobrutinib)
MONITOR: Coadministration with pirtobrutinib may increase the plasma concentrations of drugs that are substrates of CYP450 2C8, 2C19, 3A4, P-glycoprotein (P-gp), and/or breast cancer resistance protein (BCRP). The peak plasma concentration (Cmax) and systemic exposure (AUC) of repaglinide, a CYP450 2C8 substrate, increased by 98% and 130%, respectively, and the Cmax and AUC of omeprazole, a CYP450 2C19 substrate, increased by 49% and 56%, respectively, when administered with pirtobrutinib. The Cmax and AUC of oral midazolam, a CYP450 3A4 substrate, increased by 58% and 70%, respectively, while exposure to IV midazolam was not significantly affected, when administered with pirtobrutinib. The Cmax and AUC of digoxin, a P-gp substrate, increased by 51% and 17%, respectively, when administered with a single pirtobrutinib dose (200 mg), and 55% and 35%, respectively, when administered with multiple pirtobrutinib doses (200 mg daily). The Cmax and AUC of rosuvastatin, a BCRP substrate, increased by 146% and 140%, respectively, when administered with pirtobrutinib. The risk of adverse reactions related to these substrates may be increased.
MANAGEMENT: Caution is advised if pirtobrutinib is used concomitantly with substrates of CYP450 2C8, 2C19, 3A4, P-gp, and/or BCRP, particularly sensitive substrates or those with a narrow therapeutic range. The prescribing information for concomitant medications should be consulted to assess the benefits versus risks of coadministration and for any dosage adjustments that may be required.
References (1)
- (2023) "Product Information. Jaypirca (pirtobrutinib)." Lilly, Eli and Company
Drug and food interactions
pirtobrutinib food
Applies to: Jaypirca (pirtobrutinib)
GENERALLY AVOID: Grapefruit juice may increase the plasma concentrations of pirtobrutinib, which is primarily metabolized by CYP450 3A4. The proposed mechanism is inhibition of CYP450 3A4-mediated first-pass metabolism in the gut wall by certain compounds present in grapefruit. Inhibition of hepatic CYP450 3A4 may also contribute. The interaction has not been studied with grapefruit juice but has been reported for other CYP450 3A4 inhibitors. When pirtobrutinib (200 mg single dose) was administered with itraconazole, a potent CYP450 3A4 inhibitor, pirtobrutinib systemic exposure (AUC) increased by 49%. Concomitant use of diltiazem or verapamil, moderate CYP450 3A4 inhibitors, is predicted to increase pirtobrutinib AUC by 20% and 30%, respectively. 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. Increased exposure to pirtobrutinib may increase the risk of infection, bruising, bleeding, fatigue, musculoskeletal pain, diarrhea, edema, and dyspnea.
MANAGEMENT: It may be advisable for patients to avoid consumption of grapefruit, grapefruit juice, or supplements that contain grapefruit during treatment with pirtobrutinib.
References (1)
- (2023) "Product Information. Jaypirca (pirtobrutinib)." Lilly, Eli and Company
riociguat food
Applies to: riociguat
ADJUST DOSE: Smoking may decrease the plasma concentrations of riociguat. The proposed mechanism is induction of the CYP450 1A1-mediated metabolism of riociguat by polycyclic aromatic hydrocarbons present in cigarette smoke. CYP450 1A1 is responsible for the formation of the major active metabolite, M1, which has just 1/3 to 1/10 the pharmacologic activity of riociguat. According to the product labeling, plasma concentrations of riociguat are reduced by 50% to 60% in smokers compared to nonsmokers.
MANAGEMENT: Patients should be advised to stop smoking. Riociguat dosages higher than 2.5 mg three times a day may be considered in cigarette smokers, if tolerated, to match the exposure seen in nonsmoking patients. However, safety and effectiveness of higher dosages have not been established. A dosage reduction should be considered in patients who stop smoking during treatment with riociguat. The tablet form of riociguat can generally be taken with or without food. Some authorities recommend not to switch between fed and fasted riociguat intake because of increased peak plasma levels of riociguat in the fasting compared to the fed state.
References (3)
- (2013) "Product Information. Adempas (riociguat)." Bayer Pharmaceutical Inc
- (2023) "Product Information. Adempas (riociguat)." Merck Sharp & Dohme (UK) Ltd
- (2014) "Product Information. Adempas (riociguat)." Bayer Australia Limited
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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