.
Combination drugs: Kalten®, Moducren®, Moduretic®
Amiloride is a potassium-sparing (prevents excess loss of potassium) diuretic drug. 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.
Interactions with Dietary Supplements
Folic acid
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.1 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 amiloride may reduce the urinary excretion of
magnesium.2 It is unknown if this same effect would occur in humans. Nevertheless,
persons taking more than 300 mg of magnesium per day and amiloride should consult with a
doctor, as this combination may lead to potentially dangerous elevations in levels of
magnesium in the body. The combination of amiloride and hydrochlorothiazide would likely eliminate this problem,
as hydrochlorothiazide may deplete magnesium.
Potassium
As a potassium-sparing drug, amiloride reduces urinary loss of potassium.3 This can
cause potassium levels to build up in the body. People taking this drug should avoid use of
potassium chloride–containing products, such as Morton Salt Substitute®, No
Salt®, Lite Salt®, and others. Even eating several pieces of fruit per day can sometimes cause problems for people taking
potassium-sparing diuretics, due to the high potassium content of fruit.
Sodium
Diuretics, including amiloride, cause increased loss of sodium in urine. By removing sodium
from the body, diuretics cause water to leave the body as well. This reduction of water in the
body is the purpose of taking amiloride. Therefore, there is usually no reason to replace lost
sodium, although strict limitation of salt intake in combination with the action 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 the dose of their diuretics lowered.
Summary of Interactions for Amiloride
| Depletion or interference | None known |
|---|---|
| Adverse interaction | Magnesium* Potassium |
| Side effect reduction/prevention | None known |
| Supportive interaction | None known |
| Reduced drug absorption/bioavailability | None known |
| Other (see text) | Sodium |
For the convenience of the reader, the information in the summary is categorized as follows: “Depletion or interference” indicates the drug may deplete or interfere with the absorption or function of the supplement or herb. “Adverse interaction” indicates that the supplement or herb used together with the drug may result in undesirable effects. “Side effect reduction/prevention” indicates the supplement or herb may reduce the likelihood and/or severity of a potential side effect caused by the drug. “Supportive interaction” indicates the supplement or herb may support or aid the function of the drug. “Reduced drug absorption/bioavailability” indicates that the supplement or herb may decrease the absorption and/or activity of the drug in the body. An asterisk (*) next to an item in the summary indicates that the interaction is supported only by weak, fragmentary, and/or contradictory scientific evidence.
References:
1. 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.
2. 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.
3. Ramsay LE, Hettiarachchi J, Fraser R, Morton JJ. Amiloride, spironolactone, and potassium chloride in thiazide-treated hypertensive patients. Clin Pharmacol Ther 1980;27:533–43.
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