Azilsartan Medoxomil with Trimethoprim Interaction Details
Brand Names Associated with Azilsartan Medoxomil
- Azilsartan
- Edarbi®
- Edarbyclor® (as a combination product containing Azilsartan, Chlorthalidone)
Brand Names Associated with Trimethoprim
- Primsol®
- Proloprim®
- Trimethoprim
- Trimpex®

Medical Content Editor Dr. Brian Staiger, PharmD
Last updated
Mar 05, 2024
Interaction Effect
Increased risk of hyperkalemia
Interaction Summary
Coadministration of trimethoprim with drugs known to induce hyperkalemia, including potassium-sparing agents, may result in increased risk of hyperkalemia[1]. In a population based, nested, case-control study (N=165,754), sulfamethoxazole/trimethoprim was found to be 12 times more likely to cause hyperkalemia in elderly patients than amoxicillin [2]. Two cases of hyperkalemia have been reported in patients who were taking trimethoprim/sulfamethoxazole concomitantly with an ACE inhibitor. If coadministration of trimethoprim with a potassium-sparing drug is necessary, close monitoring of serum potassium is warranted in such patients [1].
Severity
Major
Onset
Unspecified
Evidence
Theoretical
How To Manage Interaction
Concomitant use of trimethoprim with drugs known to induce hyperkalemia, including potassium-sparing agents, may result in increased risk of hyperkalemia. Closely monitor serum potassium in patients who are coadministered trimethoprim with a potassium-sparing drug[1].
Mechanism Of Interaction
Additive effects of hyperkalemia
Literature Reports
A) In a population based, nested, case-control study of patients aged 66 years or older administered spironolactone, 6903 of 165,754 patients were admitted to the hospital for hyperkalemia. Among them, 161 were admitted within 14 days of receiving sulfamethoxazole/trimethoprim. Primary analysis revealed an increased risk of hospital admission for hyperkalemia in patients administered sulfamethoxazole/trimethoprim and spironolactone compared with matching controls. An adjusted analysis shown that patients admitted with hyperkalemia were 12.4 times more likely to have received a prescription for sulfamethoxazole/trimethoprim than amoxicillin. In addition, a higher risk of hospital admission was associated with a double-strength formulation of sulfamethoxazole/trimethoprim when compared with single-strength tablets (13.5 vs 9.7-fold increased risk). Analysis also determined, based on the population attributable fraction, that approximately 60% of all hyperkalemia cases in older patients treated with antibiotics for urinary infection would not have taken place if sulfamethoxazole/trimethoprim was not prescribed [2].
B) Hyperkalemia levels greater than 7 mEq/L associated with azotemia (BUN, 33 mg/dL; SCr, 3.3 mg/dL) was noted 20 days after addition of trimethoprim/sulfamethoxazole for mild acute pyelonephritis to a stable, 3-year regimen of quinapril 20 mg daily in a 74-year-old man being treated for hypertension. The patient was asymptomatic; an ECG did not reflect classic signs of hyperkalemia. Drug withdrawal and specific treatment for hyperkalemia, including insulin, dextrose, sodium polystyrene sulfonate, and calcium, was required, with resolution over 36 hours. Nifedipine was substituted for blood pressure control [3].
C) A 40-year-old woman with double lung transplantation developed a Pneumocystis infection 1 year post-transplant. Medications she was stabilized on included enalapril 30 mg daily. High dose trimethoprim/sulfamethoxazole therapy (20 mg/kg/day and 100 mg/kg/day) was instituted. After 9 days of concurrent therapy with trimethoprim/sulfamethoxazole and enalapril, the patient's potassium level reached 6.8 mmol/L. Both medications were discontinued and the patient required treatment for her hyperkalemic condition [4].
References
1 ) Product Information: SEPTRA(R) DS oral double strength tablets, trimethoprim sulfamethoxazole oral double strength tablets. Monarch Pharmaceuticals, Inc. (per FDA), New York, NY, 2013.
2 ) Antoniou T, Gomes T, Mamdani MM, et al: Trimethoprim-sulfamethoxazole induced hyperkalaemia in elderly patients receiving spironolactone: nested case-control study. BMJ 2011; 343:d5228-.PubMed Abstract: http://www.ncbi.nlm.nih.gov/...
3 ) Thomas RJ: Severe hyperkalemia with trimethoprim-quinapril. Ann Pharmacother 1996; 30:413-414.
4 ) Bugge JF: Severe hyperkalaemia induced by trimethoprim in combination with an angiotensin-converting enzyme inhibitor in a patient with transplanted lungs. J Intern Med 1996; 240:249-251.
Azilsartan Medoxomil Overview
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Azilsartan is used alone or in combination with other medications to treat high blood pressure. Azilsartan is in a class of medications called angiotensin II receptor antagonists. It works by blocking the action of certain natural substances that tighten the blood vessels, allowing the blood to flow more smoothly and the heart to pump more efficiently.
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High blood pressure is a common condition, and when not treated it can cause damage to the brain, heart, blood vessels, kidneys, and other parts of the body. Damage to these organs may cause heart disease, a heart attack, heart failure, stroke, kidney failure, loss of vision, and other problems. In addition to taking medication, making lifestyle changes will also help to control your blood pressure. These changes include eating a diet that is low in fat and salt, maintaining a healthy weight, exercising at least 30 minutes most days, not smoking, and using alcohol in moderation.
Trimethoprim Overview
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Trimethoprim eliminates bacteria that cause urinary tract infections. It is used in combination with other drugs to treat certain types of pneumonia. It also is used to treat traveler's diarrhea. Antibiotics will not work for colds, flu, or other viral infections.
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This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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Definitions
Severity Categories
Contraindicated
These drugs, generally, should not be used together simultaneously due to the high risk of severe adverse effects. Combining these medications can lead to dangerous health outcomes and should be strictly avoided unless otherwise instructed by your provider.
Major
This interaction could result in very serious and potentially life-threatening consequences. If you are taking this drug combination, it is very important to be under close medical supervision to minimize severe side effects and ensure your safety. It may be necessary to change a medication or dosage to prevent harm.
Moderate
This interaction has the potential to worsen your medical condition or alter the effectiveness of your treatment. It's important that you are monitored closely and you potentially may need to make adjustments in your treatment plan or drug dosage to maintain optimal health.
Minor
While this interaction is unlikely to cause significant problems, it could intensify side effects or reduce the effectiveness of one or both medications. Monitoring for changes in symptoms and your condition is recommended, and adjustments may be made if needed to manage any increased or more pronounced side effects.
Onset
Rapid: Onset of drug interaction typically occurs within 24 hours of co-administration.
Delayed: Onset of drug interaction typically occurs more than 24 hours after co-administration.
Evidence
Level of documentation of the interaction.
Established: The interaction is documented and substantiated in peer-reviewed medical literature.
Theoretical: This interaction is not fully supported by current medical evidence or well-documented sources, but it is based on known drug mechanisms, drug effects, and other relevant information.
How To Manage The Interaction
Provides a detailed discussion on how patients and clinicians can approach the identified drug interaction as well as offers guidance on what to expect and strategies to potentially mitigate the effects of the interaction. This may include recommendations on adjusting medication dosages, altering the timing of drug administration, or closely monitoring for specific symptoms.
It's important to note that all medical situations are unique, and management approaches should be tailored to individual circumstances. Patients should always consult their healthcare provider for personalized advice and guidance on managing drug interactions effectively.
Mechanism Of Interaction
The theorized or clinically determined reason (i.e., mechanism) why the drug-drug interaction occurs.
Disclaimer: The information provided on this page is for informational purposes only and should not be considered medical advice. Always consult with a qualified healthcare professional regarding your specific circumstances and medical conditions.
Where Does Our Information Come From?
Information for our drug interactions is compiled from several drug compendia, including:
The prescribing information for each drug, as published on DailyMED, is also used.
Individual drug-drug interaction detail pages contain references specific to that interaction. You can click on the reference number within brackets '[]' to see what reference was utilized.
The information posted is fact-checked by HelloPharmacist clinicians and reviewed quarterly.