Drug Interactions between abiraterone and spironolactone
This report displays the potential drug interactions for the following 2 drugs:
- abiraterone
- spironolactone
Interactions between your drugs
spironolactone abiraterone
Applies to: spironolactone and abiraterone
GENERALLY AVOID: Concomitant use of abiraterone and spironolactone may increase prostate specific antigen (PSA) levels and shorten progression free survival time in patients undergoing treatment for prostate cancer. The exact mechanism is unknown, but experimental evidence suggests that in an androgen-depleted environment spironolactone switches from being anti-androgenic to acting as an androgen receptor agonist. In the three randomized placebo-controlled international clinical studies that demonstrated the safety and efficacy of abiraterone with prednisone, concurrent spironolactone use was not allowed during the study period due to this potential interaction. Additionally, there are several case studies in patients who used spironolactone concurrently with abiraterone during metastatic castration-resistant prostate cancer where tumor progression was observed and thought to be a direct result of this interaction. While eplerenone is similar to spironolactone in its mechanism of action, evidence as to whether or not it can also act as an androgen receptor agonist is conflicting, with some in vitro studies suggesting that it is able to activate certain androgen receptors.
MANAGEMENT: Concomitant use of abiraterone and spironolactone in patients with metastatic castration-resistant prostate cancer is not recommended. If this combination is used, monitoring for worsening clinical symptoms and increased levels of biochemical markers for prostate cancer such as PSA and alkaline phosphatase levels should be considered. Some authorities suggest using a combination of amiloride with hydrochlorothiazide if medications that do not activate androgen receptors, but can potentially treat symptoms of increased mineralocorticoid levels (e.g., hypertension, hypokalemia, fluid retention) are needed.
References (14)
- Sundar S, Dickinson PD (2012) "Spironolactone, a possible selective androgen receptor modulator, should be used with caution in patients with metastatic carcinoma of the prostate." BMJ Case Rep, 2012, p. 1-4
- Ferraldeschi R, Sharifi N, Auchus RJ, Attard G (2013) "Molecular pathways: Inhibiting steroid biosynthesis in prostate cancer." Clin Cancer Res, 19, p. 3353-9
- (2023) "Product Information. Akeega (abiraterone-niraparib)." Janssen Biotech, Inc.
- (2021) "Product Information. Zytiga (abiraterone)." Janssen Biotech, Inc.
- (2022) "Product Information. Yonsa (abiraterone)." Sun Pharmaceutical Industries
- (2023) "Product Information. Apo-Abiraterone (abiraterone)." Apotex Inc
- (2021) "Product Information. Zytiga (abiraterone)." Janssen-Cilag Pty Ltd
- (2023) "Product Information. Abiraterone (abiraterone)." Wockhardt UK Ltd
- (2023) "Product Information. Yonsa Mpred (abiraterone-methylprednisolone)." Sun Pharma ANZ Pty Ltd
- Vicente-Valor J, Escudero-Vilaplana V, Collado-Borrell R, et al. (2022) "Potential negative pharmacodynamic interaction of spironolactone and abiraterone in two prostate cancer patients." J Oncol Pharm Pract, 28, p. 1259-63
- Dhondt B, Buelens S, Van Besien J, et al. (2023) Abiraterone and spironolactone in prostate cancer: a combination to avoid. https://www.tandfonline.com/doi/abs/10.1080/17843286.2018.1543827
- Richards J, lim ac, Hay CW, et al. (2012) "Interactions of abiraterone, eplerenone and prednisolone with wild-type and mutant androgen receptor: a rationale for increasing abiraterone exposure or combining with MDV3100." Cancer Res, 72, p. 2176-82
- gill d, Gaston D, bailey e, et al. (2017) "Efficacy of eplerenone in the management of mineralocorticoid excess in men with metastatic castration resistant prostate cancer treated with abiraterone without prednisone." Clin Genitourin Cancer, 15, e599-2
- Decamps S, Lis R, Ekanayake P (2023) "Abirateron-induced endocrinopathies." JCEM Case Reports, 1, p. 1-4
Drug and food interactions
abiraterone food
Applies to: abiraterone
ADJUST DOSING INTERVAL: Food may significantly increase the oral bioavailability of some formulations of abiraterone acetate. Compared to administration in the fasted state, abiraterone peak plasma concentration (Cmax) and systemic exposure (AUC) were approximately 7- and 5-fold higher, respectively, when a single dose of abiraterone acetate was administered with a low-fat meal (7% fat; 300 calories) and approximately 17- and 10-fold higher, respectively, when it was administered with a high-fat meal (57% fat; 825 calories). Given the normal variation in the content and composition of meals, taking abiraterone acetate with meals has the potential to result in increased and highly variable exposures. The safety of these increased exposures during multiple dosing has not been assessed. However, the abiraterone acetate 125 mg tablet, commonly marketed as Yonsa, was found to have an approximately 6.5-fold higher Cmax and 4.4-fold higher AUC when a single dose of 500 mg (4 tablets) was administered with a high-fat meal (56% - 60% fat, 900 - 1000 calories) compared to overnight fasting in healthy volunteers. These differences were not considered clinically significant for this formulation.
MANAGEMENT: Some formulations of abiraterone acetate must be taken on an empty stomach. No food should be consumed for at least two hours before and one hour after the abiraterone acetate dose. However, the abiraterone acetate 125 mg tablet, commonly marketed as Yonsa, can be taken with or without food. The manufacturer's product labeling should be consulted for specific guidance.
References (9)
- (2011) "Product Information. Zytiga (abiraterone)." Centocor Inc
- (2023) "Product Information. Akeega (abiraterone-niraparib)." Janssen Biotech, Inc.
- (2023) "Product Information. Akeega (abiraterone-niraparib)." Janssen Inc
- (2021) "Product Information. Zytiga (abiraterone)." Janssen Biotech, Inc.
- (2022) "Product Information. Yonsa (abiraterone)." Sun Pharmaceutical Industries
- (2023) "Product Information. Apo-Abiraterone (abiraterone)." Apotex Inc
- (2021) "Product Information. Zytiga (abiraterone)." Janssen-Cilag Pty Ltd
- (2023) "Product Information. Abiraterone (abiraterone)." Wockhardt UK Ltd
- (2023) "Product Information. Yonsa Mpred (abiraterone-methylprednisolone)." Sun Pharma ANZ Pty Ltd
spironolactone food
Applies to: spironolactone
MONITOR: Many psychotherapeutic and CNS-active agents (e.g., anxiolytics, sedatives, hypnotics, antidepressants, antipsychotics, opioids, alcohol, muscle relaxants) exhibit hypotensive effects, especially during initiation of therapy and dose escalation. Coadministration with antihypertensives and other hypotensive agents, in particular vasodilators and alpha-blockers, may result in additive effects on blood pressure and orthostasis.
MANAGEMENT: Caution and close monitoring for development of hypotension is advised during coadministration of these agents. Some authorities recommend avoiding alcohol in patients receiving vasodilating antihypertensive drugs. Patients should be advised to avoid rising abruptly from a sitting or recumbent position and to notify their physician if they experience dizziness, lightheadedness, syncope, orthostasis, or tachycardia. Patients should also avoid driving or operating hazardous machinery until they know how the medications affect them.
References (10)
- Sternbach H (1991) "Fluoxetine-associated potentiation of calcium-channel blockers." J Clin Psychopharmacol, 11, p. 390-1
- Shook TL, Kirshenbaum JM, Hundley RF, Shorey JM, Lamas GA (1984) "Ethanol intoxication complicating intravenous nitroglycerin therapy." Ann Intern Med, 101, p. 498-9
- Feder R (1991) "Bradycardia and syncope induced by fluoxetine." J Clin Psychiatry, 52, p. 139
- Ellison JM, Milofsky JE, Ely E (1990) "Fluoxetine-induced bradycardia and syncope in two patients." J Clin Psychiatry, 51, p. 385-6
- Rodriguez de la Torre B, Dreher J, Malevany I, et al. (2001) "Serum levels and cardiovascular effects of tricyclic antidepressants and selective serotonin reuptake inhibitors in depressed patients." Ther Drug Monit, 23, p. 435-40
- Cerner Multum, Inc. "Australian Product Information."
- Pacher P, Kecskemeti V (2004) "Cardiovascular side effects of new antidepressants and antipsychotics: new drugs, old concerns?" Curr Pharm Des, 10, p. 2463-75
- Andrews C, Pinner G (1998) "Postural hypotension induced by paroxetine." BMJ, 316, p. 595
- (2023) "Product Information. Buprenorphine (buprenorphine)." G.L. Pharma UK Ltd
- (2023) "Product Information. Temgesic (buprenorphine)." Reckitt Benckiser Pty Ltd
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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