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Drug Interactions between capivasertib and Cycloset

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

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Interactions between your drugs

Major

bromocriptine capivasertib

Applies to: Cycloset (bromocriptine) and capivasertib

MONITOR CLOSELY: Capivasertib may interfere with the therapeutic effects of insulin and/or antidiabetic agents. Fluctuations in blood glucose levels may be related to capivasertib-mediated inhibition of the serine/threonine kinase (AKT) pathway, a critical regulator of glucose metabolism. Hypoglycemia and hyperglycemia, including diabetic ketoacidosis (DKA) and fatal outcomes, have been reported and may occur at any point during treatment. However, the median time to the first occurrence of hyperglycemia was reported at 15 days after starting capivasertib. In addition, in some cases, DKA was observed within 10 days after commencing capivasertib. In the phase 3 randomized, double-blind, placebo-controlled trial, CAPItello-291, 12% of patients who received capivasertib had an anti-hyperglycemic medication regimen either initiated or modified during the study, including treatment with insulin in 4.8% of patients. However, clinical data are lacking in patients with Type 1 diabetes, Type 2 diabetes requiring insulin or those with a glycated hemoglobin (HbA1c) of 8%, as they were excluded from the CAPItello-291 trial.

MANAGEMENT: Glycemic status, including fasting plasma glucose and/or HbA1c, should be assessed prior to the initiation of capivasertib therapy and closely monitored during and after discontinuation of therapy, especially in those receiving insulin or other antidiabetic agents. Patients should learn to recognize the symptoms of hypoglycemia such as headache, dizziness, drowsiness, nervousness, confusion, tremor, hunger, weakness, perspiration, palpitation, and tachycardia. If hypo-or hyperglycemia occurs during capivasertib therapy, patients should be initiated on appropriate remedial therapy immediately. The manufacturer's product labeling should also be consulted for specific management and dosage adjustment guidance.

References (5)
  1. (2023) "Product Information. Truqap (capivasertib)." Astra-Zeneca Pharmaceuticals
  2. (2024) "Product Information. Truqap (capivasertib)." AstraZeneca Pty Ltd
  3. (2025) "Product Information. Truqap (capivasertib)." AstraZeneca Canada Inc
  4. Government of Canada (2025) Regulatory decision summary for truqap. https://dhpp.hpfb-dgpsa.ca/review-documents/resource/RDS1718733982360
  5. (2025) "Product Information. Truqap (capivasertib)." AstraZeneca UK Ltd

Drug and food/lifestyle interactions

Major

capivasertib food/lifestyle

Applies to: capivasertib

GENERALLY AVOID: Grapefruit juice may increase the plasma concentrations of capivasertib, 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 studied with other CYP450 3A4 inhibitors. Based on clinical studies and model-informed approaches, concomitant use with the potent CYP450 3A4 inhibitor itraconazole is predicted to increase capivasertib systemic exposure (AUC) by up to 1.7-fold and peak plasma concentration (Cmax) by up to 1.4-fold. Coadministration with the moderate CYP450 3A4 inhibitors erythromycin and verapamil is predicted to increase the AUC and Cmax of capivasertib by up to 1.5-fold 1.3-fold, 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 capivasertib may increase the risk of adverse effects such as diarrhea, cutaneous adverse reactions, decreased lymphocytes, decreased hemoglobin, hyperglycemia, nausea, and fatigue.

MANAGEMENT: It may be advisable for patients to avoid the consumption of grapefruit, grapefruit juice, or supplements that contain grapefruit during treatment with capivasertib.

References (1)
  1. (2023) "Product Information. Truqap (capivasertib)." Astra-Zeneca Pharmaceuticals
Moderate

bromocriptine food/lifestyle

Applies to: Cycloset (bromocriptine)

GENERALLY AVOID: Alcohol may potentiate some of the pharmacologic effects of CNS-active agents. Use in combination may result in additive central nervous system depression and/or impairment of judgment, thinking, and psychomotor skills.

MANAGEMENT: Patients receiving CNS-active agents should be warned of this interaction and advised to avoid or limit consumption of alcohol. Ambulatory patients should be counseled to avoid hazardous activities requiring complete mental alertness and motor coordination until they know how these agents affect them, and to notify their physician if they experience excessive or prolonged CNS effects that interfere with their normal activities.

References (4)
  1. Warrington SJ, Ankier SI, Turner P (1986) "Evaluation of possible interactions between ethanol and trazodone or amitriptyline." Neuropsychobiology, 15, p. 31-7
  2. Gilman AG, eds., Nies AS, Rall TW, Taylor P (1990) "Goodman and Gilman's the Pharmacological Basis of Therapeutics." New York, NY: Pergamon Press Inc.
  3. (2012) "Product Information. Fycompa (perampanel)." Eisai Inc
  4. (2015) "Product Information. Rexulti (brexpiprazole)." Otsuka American Pharmaceuticals Inc
Moderate

bromocriptine food/lifestyle

Applies to: Cycloset (bromocriptine)

MONITOR: Nicotine may cause vasoconstriction in some patients and potentiate the ischemic response to ergot alkaloids.

MANAGEMENT: Caution may be advisable when ergot alkaloids are used in combination with nicotine products. Patients should be advised to seek immediate medical attention if they experience potential symptoms of ischemia such as coldness, pallor, cyanosis, numbness, tingling, or pain in the extremities; muscle weakness; severe or worsening headache; visual disturbances; severe abdominal pain; chest pain; and shortness of breath.

References (4)
  1. (2001) "Product Information. Migranal (dihydroergotamine nasal)." Novartis Pharmaceuticals
  2. (2004) "Product Information. Cafergot (caffeine-ergotamine)." Novartis Pharmaceuticals
  3. Cerner Multum, Inc. "UK Summary of Product Characteristics."
  4. Cerner Multum, Inc. "Australian Product Information."

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.