Abstract
Torasemide and furosemide are representatives of the loop diuretics with the same mechanism of action. They belong to the group of sulfonyl benzoic acid. Differences in the chemical structure make these drugs have different pharmacokinetic properties and an additive effect. Torasemide in comparison with furosemide has a higher bioavailability, high protein binding, and the longer half-life. These properties make torasmide work faster, longer and less frequently cause rapid micturition than furosemide. Torasemide after oral administration is well absorbed from the gastrointestinal tract even in situations of fluid overload in diseases of the heart, kidneys and liver. Torasemide potency is four times greater than the furosemide. The dose of 40 mg of furosemide is equivalent to the 10 mg of torasemide. Torasemide has additionally antialdosteron effect and inhibits the process of fibrosis and myocardial remodeling.
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