Triamterene is a potassium-sparing diuretic (i.e., it inhibits the urinary excretion of potassium). Diuretics increase urinary water loss from the body and are used to treat high blood pressure, congestive heart failure, and some kidney or liver conditions. Triamterene is available as a single agent and in combination products.
Safetychecker Summary
for Triamterene
(for details about the summarized interactions, read the full article)
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Calcium* Folic acid* |
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Folic acid |
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Buchu Cleavers Dandelion Gravel root Horsetail Juniper Magnesium Potassium Uva ursi |
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Sodium |
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| Supportive interaction |
None known |
| Reduced drug absorption/bioavailability |
None known |
Interactions with Dietary Supplements
Calcium
A review of the research literature indicates that triamterene may increase calcium
loss.1 The importance of this information is unclear.
Folic
acid
Triamterene is a weak folic acid antagonist that has been associated with folic
acid-deficiency anemia in people already at risk for folic acid deficiency.2
However, people treated long term with triamterene, without additional risk for folic acid
deficiency, were found to have normal folic acid levels and no signs of folic acid
deficiency.3 The use of
multivitamin supplements containing folic acid appears to diminish the occurrence of birth defects associated with triamterene.
According to one study,4 pregnant
women who took folic acid–containing multivitamin supplements in addition to their
prescription drugs had fewer babies with heart defects and deformities of the upper lip and
mouth.
One study showed that people taking diuretics for more than six months had dramatically lower blood levels of folic acid and higher levels of homocysteine compared with individuals not taking diuretics.5 Homocysteine, a toxic amino acid byproduct, has been associated with atherosclerosis. Until further information is available, people taking diuretics for longer than six months should probably supplement with folic acid.
Magnesium
Preliminary research in animals suggests that triamterene may inhibit the urinary excretion of
magnesium.6 It is unknown if this same effect would occur in humans. Persons taking
more than 300 mg of magnesium per day and triamterene should consult with a doctor as this
combination may lead to potentially dangerous increases in the level of magnesium in the body.
The combination of triamterene and
hydrochlorothiazide would likely eliminate this problem, as hydrochlorothiazide may
deplete magnesium.
Potassium
As a potassium-sparing drug, triamterene reduces urinary loss of potassium, which can lead to
elevated potassium levels.7 People taking triamterene should avoid potassium
supplements, potassium-containing salt substitutes (Morton Salt Substitute®, No
Salt®, Lite Salt®, and others) and even high-potassium foods (primarily fruit). Doctors should monitor potassium blood levels
in patients taking triamterene to prevent problems associated with elevated potassium
levels.
Sodium
Diuretics, including triamterene, cause
increased loss of sodium in the urine. By removing sodium from the body, diuretics also cause
water to leave the body. This reduction of body water is the purpose of taking diuretics.
Therefore, there is usually no reason to replace lost sodium, although strict limitation of
salt intake in combination with the actions of diuretics can sometimes cause excessive sodium
depletion. On the other hand, people who restrict
sodium intake and in the process reduce blood pressure may need to have their dose of
diuretics lowered. People taking triamterene should talk with their prescribing doctor before
severely restricting salt.
Interactions with Herbs
Diuretic herbs
Herbs that have a diuretic effect should be avoided when taking diuretic medications, as they
may enhance the effect of these drugs and lead to possible cardiovascular side effects. These
herbs include dandelion, uva ursi,
juniper, buchu, cleavers,
horsetail, and gravel root.8
1. Werbach WR. Foundations of Nutritional Medicine. Tarzana, CA: Third Line Press, 1997, 246 [review].
2. Jackson EK. Diuretics. In Goodman & Gilman’s The Pharmacological Basis of Therapeutics, 9th ed. New York: McGraw Hill, 1996, 706.
3. Mason JB, Zimmerman J, Otradovec CL, et al. Chronic diuretic therapy with moderate doses of triamterene is not associated with folate deficiency. J Lab Clin Med 1991;117:365–9.
4. Hernández-Díaz S, Werler MM, Walker AM, Mitchell AA. Folic acid antagonists during pregnancy and the risk of birth defects. N Engl J Med 2000;343:1608–14.
5. Morrow LE, Grimsley EW. Long-term diuretic therapy in hypertensive patients: effects on serum homocysteine, vitamin B6, vitamin B12, and red blood cell folate concentrations. South Med J 1999;92:866–70.
6. Devane J, Ryan MP. The effects of amiloride and triamterene on urinary magnesium excretion in conscious saline-loaded rats. Br J Pharmacol 1981;72:285–9.
7. Jackson PR, Ramsay LE, Wakefield V. Relative potency of spironolactone, triamterene and potassium chloride in thiazide-induced hypokalaemia. Br J Clin Pharmacol 1982;14:257–63.
8. Brinker F. Herb Contraindications and Drug Interactions. Sandy, OR: Eclectic Institute, 1997, 102–3.
9. Threlkeld DS, ed. Diuretics and Cardiovasculars, Potassium-Sparing Diuretics, Triamterene. In Facts and Comparisons Drug Information. St. Louis, MO: Facts and Comparisons, Jul 1993, 138k–9.
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The information presented in Healthnotes is for informational purposes only. It is based on scientific studies (human, animal, or in vitro), clinical experience, or traditional usage as cited in each article. The results reported may not necessarily occur in all individuals. For many of the conditions discussed, treatment with prescription or over-the-counter medication is also available. Consult your doctor, practitioner, and/or pharmacist for any health problem and before using any supplements or before making any changes in prescribed medications. Information expires December 2003.