Diuretics: Generic and Brand Names
Diuretics: Generic and Brand Names
Diuretics: Generic and Brand Names
Description/General Information
o Diuretics are used for two main purposes: to decrease hypertension (lower blood pressure)
and to decrease edema, typically peripheral and pulmonary, in heart failure (HF) and renal
or liver disorders.
o Diuretics are drugs that primarily increase the excretion of sodium. To some extent, they
also increase the volume of urine produced by the kidneys.
o By blocking the absorptive capacity of cells lining the renal tubules for sodium, intravascular
volume and the eventual leaking of fluid from capillaries is reduced and prevented.
o It is used in the management of diseases like glaucoma, hypertension, and edema in heart
failure, liver failure, and renal diseases.
Thiazide diuretics
bendroflumethiazide Naturetin
chlorothiazide Diuril
hydroflumethiazide Saluron
methyclothiazide Enduron
indapamide Lozol
metolazone Mykrox, Zaroxolyn
bumetanide Bumex
torsemide Demadex
acetazolamide Diamox
amiloride Midamor
triamterene Dyrenium
o Nursing Diagnoses
Fluid Volume, Risk for Deficient
Elimination, Impaired Urinary related to kidney dysfunction
Fluid Volume, Excess related to body fluid retention
o Planning
The patient’s blood pressure will be decreased or will return to a normal
value.
The patient’s edema will be decreased.
The patient’s serum chemistry levels will remain within normal ranges.
o Nursing Interventions
Monitor vital signs and serum electrolytes, especially potassium, glucose,
uric acid, and cholesterol levels. Report changes. If a patient is taking
digoxin and hypokalemia occurs, digitalis toxicity frequently results.
Observe for signs and symptoms of hypokalemia such as muscle
weakness, leg cramps, and cardiac dysrhythmias.
Monitor the patient’s weight daily. A weight gain of 2.2 lb is equivalent
to 1 L of body fluids.
Note urine output to determine fluid loss or retention.
o Evaluation
Evaluate the effectiveness of drug therapy. The patient’s blood pressure
and edema will be reduced, and blood chemistry will remain within
normal range.
Determine an absence of side effects and adverse reactions to therapy.
Pharmacotherapeutic action
o It causes active pumping out of chloride from the cells lining the
ascending limb of Loop of Henle and distal tubule by blocking the
chloride pump. Since sodium passively moves with chloride to
maintain electrical neutrality, both sodium and chloride are excreted
in the urine.
Pharmacodynamic action
o Thiazides act directly on arterioles to cause vasodilation, which can lower blood
pressure.
o Other action includes the promotion of sodium chloride and water excretion,
resulting in a decrease in vascular fluid volume and a concomitant decrease in
cardiac output and blood pressure.
o The onset of action of hydrochlorothiazide occurs within 2 hours. Peak
concentration times are long (4 hours).
o Thiazides are divided into three groups according to their duration of action: (1)
short acting (duration 24 hours).
Pharmacokinetics
o Thiazides are well absorbed from the gastrontestinal (GI) tract.
o Hydrochlorothiazide has moderate protein-binding power.
o The half-life of the thiazide drugs is longer than that of the loop diuretics.
o For this reason, thiazides should be administered in the morning to avoid nocturia
(nighttime urination) and sleep interruption.
Contraindications/caution
o Allergy to loop diuretics. Prevent severe hypersensitivity reactions.
o GI: GI upset
o GU: hypokalemia (can precipitate hyperglycemia), hypercalcemia,
hyperuremia, slightly-alkalinized urine (can lead to bladder infections)
chlorothiazide Diuril
hydrochlorothiazide HydroDIURIL
hydroflumethiazide Saluron
methyclothiazide Enduron
chlorthalidone Hygroton
Nursing management
o Assessment
Obtain a history of drugs taken daily. Note if the patient is taking a drug
that may interact with a loop diuretic, such as alcohol, aminoglycosides,
anticoagulants, corticosteroids, lithium, amphotericin B, or digitalis.
Recognize that furosemide is highly protein bound and can displace other
protein-bound drugs such as warfarin.
Assess vital signs, serum electrolytes, weight, and urine output for
baseline levels.
Compare the patient’s drug dose with the recommended dose, and report
any discrepancy.
Note whether the patient is hypersensitive to sulfonamides. Nursing
o Diagnoses
Fluid Volume, Risk for Deficient
Electrolyte Imbalance, Risk for
o Planning
The patient’s edema and/or hypertension will be decreased.
The patient’s serum chemistry levels will remain within normal ranges.
o Nursing Interventions
Monitor urinary output to determine body fluid gain or loss. Urinary
output should be at least 30 mL/h or 600 mL/24 h.
Notify a health care provider if urine output does not increase; a severe
renal disorder may be present.
Weigh the patient to determine fluid loss or gain. A loss of 2.2 lb is
equivalent to a fluid loss of 1 L.
Monitor vital signs, and be alert for marked decreases in blood pressure. •
Administer IV furosemide slowly; hearing loss may occur if it is rapidly
injected.
Observe for signs and symptoms of hypokalemia (Nursing Interventions
Monitor urinary output to determine body fluid gain or loss. Urinary
output should be at least 30 mL/h or 600 mL/24 h.
Notify a health care provider if urine output does not increase; a severe
renal disorder may be present.
Weigh the patient to determine fluid loss or gain. A loss of 2.2 lb is
equivalent to a fluid loss of 1 L.
Monitor vital signs, and be alert for marked decreases in blood pressure.
Administer IV furosemide slowly; hearing loss may occur if it is rapidly
injected.
Observe for signs and symptoms of hypokalemia (<3.5 mEq/L), such as
muscle weakness,abdominal distension, leg cramps, and/or cardiac
dysrhythmias.
Pharmacotherapeutic action
o Blocks the action of chloride pump in the ascending limb of the loop of
Henle, where 30% of sodium is normally reabsorbed. This causes
decreased reabsorption of chloride and sodium.
o Exerts the same effect on the descending limb of loop of Henle and
distal tubule causing sodium-rich urine.
o
Pharmacodynamic action
o Loop diuretics have a great saluretic (sodium chloride–losing) or natriuretic
(sodium-losing) effect and can cause rapid diuresis, decreasing vascular fluid
volume and causing a decrease in cardiac output and blood pressure.
o Because furosemide is more potent than thiazide diuretics, it causes a vasodilatory
effect; thus renal blood flow increases before diuresis.
o Furosemide is used when other conservative measures, such as sodium restriction
and use of less potent diuretics, fail.
o The oral dose of furosemide is usually twice that of an intravenous (IV) dose.
o The onset of action of loop diuretics occurs within 30 to 60 minutes. The onset of
action for IV furosemide is 5 minutes.
o The duration of action is shorter than that of the thiazides
Pharmacokinetics
o Loop diuretics are rapidly absorbed by the GI tract.
o These drugs are highly protein bound with halflives that vary from 1 to 5 hours.
o Loop diuretics compete for protein-binding sites with other highly protein-bound
drugs.
Contraindications/caution
o Allergy to thiazides and sulfonamides. Prevent severe
hypersensitivity reactions.
o Electrolyte depletion. Can be potentiated by the changes in fluid and
electrolyte levels caused by diuretics.
o Severe renal failure, anuria. Exacerbated by the effects of the drug.
o Systemic lupus erythematosus (SLE). Can precipitate renal failure
because the disease already causes changes in glomerular filtration.
o Glucose tolerance abnormalities and diabetes mellitus. Worsened
by glucose-elevating effect of some diuretics
o Gout. Already reflects abnormality in tubular reabsorption and
secretion.
o Hepatic coma. Exacerbated by fluid shifts associated with drug use.
o Pregnancy, lactation. Can cause potential adverse effects to the fetus
and baby. Routine use of this drug in pregnancy is not appropriate and
should be used only when there is underlying pathological conditions.
For lactating women, an alternative method of feeding should be
instituted.
Drug interactions
o Aminoglycosides or cisplatin: increased ototoxicity effect of loop
diuretics
o Anticoagulants: increased anticoagulation effects
o GI: GI upset
o GU: hypokalemia (can precipitate hyperglycemia), increased
bicarbonate excretion (can lead to alkalosis), hypocalcemia and tetany
o EENT: ototoxicity, reversible loss of hearing
Common drugs used in the market
Loop diuretics
furosemide Lasix
torsemide Demadex
Osmotic Diuretics
o This type of diuretic exerts their therapeutic effect by pulling water
into the renal tubule without loss of sodium.
o Only one osmotic diuretic is currently available, mannitol (Osmitrol).
Action
o Osmotic diuretics increase the osmolality (concentration) and sodium
reabsorption in the proximal tubule and loop of Henle
o This group of drugs is used to prevent kidney failure, decrease intracranial
pressure (ICP, such as in cerebral edema), and decrease intraocular pressure (IOP,
such as in glaucoma
Indication
o Conditions that may aggravate fluid loss like vomiting, diarrhea, and
profuse sweating should be emphasized to them because these may
change the need for diuretics.
Pregnant women
Nursing management
o
Pharmacotherapeutic action
o Mannitol is a sugar that is not well reabsorbed by the tubules and it
acts to pull large amounts of fluid into the urine due to the osmotic
pull exerted by large sugar molecule.
o This also pulls fluid into the vascular system from extravascular spaces
like aqueous humor.
Pharmacodynamic action
Pharmacokinetics
Route Onset Peak Duration
IV 30-60 min 1h 6-8 h
o
Contraindications/caution
o Renal disease, anuria, pulmonary congestion,
intracranial bleeding, dehydration, HF. Exacerbated by large shifts
in fluid related to drug use.
o Pregnancy, lactation. Can cause potential adverse effects to the fetus
and baby. Routine use of this drug in pregnancy is not appropriate and
should be used only when there is underlying pathological conditions.
For lactating women, an alternative method of feeding should be
instituted.
o
Drug interactions
Side/adverse effects
o CNS: light-headedness, confusion, headache
Action
o The carbonic anhydrase inhibitors acetazolamide and methazolamide block the
action of the enzyme carbonic anhydrase, which is needed to maintain the body’s
acid-base balance (hydrogen and bicarbonate ion balance).
o Inhibition of this enzyme causes increased sodium, potassium, and bicarbonate
excretion.
o With prolonged use, metabolic acidosis can occur.
Indication
T1/2: 5-6 h
Metabolism: N/A
Excretion: urine (unchanged)
o
Contraindications/caution
o Allergy to carbonic anhydrase inhibitors, thiazides, antibacterial
sulfonamides. Prevent severe hypersensitivity reactions.
o Chronic noncongestive angle-closure glaucoma. Not effectively
treated by this drug.
o Fluid and electrolyte imbalance, renal or hepatic disease,
adrenocortical insufficiency, respiratory acidosis, chronic
obstructive pulmonary disease (COPD). Could be exacerbated by
fluid and electrolyte changes caused by these drugs.
o Pregnancy, lactation. Can cause potential adverse effects to the fetus
and baby. Routine use of this drug in pregnancy is not appropriate and
should be used only when there is underlying pathological conditions.
For lactating women, an alternative method of feeding should be
instituted.
Drug interactions
o Salicylate, lithium: increased excretion of these drugs
Side/adverse effects
o CNS: paresthesia, confusion, drowsiness
o CV: hypotension
o GU: hypokalemia (can precipitate hyperglycemia), increased loss of
bicarbonate (can lead to metabolic acidosis)
o
Common drugs used in the market
acetazolamide Diamox
Carbonic Anhydrase Inhibitors
methazolamide Glauctabs, MZM, Neptazane
Potassium-Sparing Diuretics
o Less powerful than loop diuretics but they retain potassium instead of
wasting it.
o Typically used for patients who have high risk for hypokalemia
associated with diuretic use.
Action
o Potassium-sparing diuretics act primarily in the collecting duct renal tubules and
late distal tubule to promote sodium and water excretion and potassium retention.
o The drugs interfere with the sodium-potassium pump controlled by the
mineralocorticoid hormone aldosterone (sodium retained and potassium excreted).
Indication
Nursing management
o Assessment •
Obtain a history of drugs taken daily. Note whether the patient is taking a
potassium supplement or using a salt substitute.
Assess vital signs, serum electrolytes, weight, and urinary output for
baseline levels.
Compare the patient’s drug dose with the recommended dose, and report
any discrepancy.
o Nursing Diagnoses
Fluid Volume, Risk for Deficient
Electrolyte Imbalance, Risk for
o Planning
The patient’s fluid retention and blood pressure will be decreased.
The patient’s serum electrolytes will remain within normal ranges.
o Nursing Interventions
Note the half-life of spironolactone. With a long half-life, the drug is
usually administered once a day, sometimes twice a day.
Monitor urinary output; it should increase. Report if urine output is less
than 30 mL/h or less than 600 mL/day.
Record vital signs and report any abnormal changes.
Observe for signs and symptoms of hyperkalemia (serum potassium >5.0
mEq/L). Nausea, diarrhea, abdominal cramps, numbness and tingling of
the hands and feet, leg cramps, tachycardia and later bradycardia, peaked
narrow T wave on electrocardiogram, or oliguria may signal
hyperkalemia.
Administer spironolactone in the morning and not in the evening to avoid
nocturia.
o Evaluation
Evaluate the effectiveness of potassium-sparing diuretics (e.g.,
triamterene). Fluid retention (edema) should be decreased or absent.
Determine whether urine output has increased and whether serum
potassium level is within the normal range
Pharmacotherapeutic action
o This type of diuretics causes a loss of sodium while promoting the
retention of potassium.
o Spironolactone acts as aldosterone antagonist which blocks the
action of aldosterone in the distal tubule. On the other
hand, amiloride and triamterene block potassium secretion through
the tubule.
o
Pharmacodynamic action
Pharmacokinetics
Route Onset Peak Duration
T1/2: 20 h
Metabolism: liver
Excretion: urine (unchanged)
o
Contraindications/caution
o Allergy to potassium-sparing diuretics. Prevent severe
hypersensitivity reactions.
o Hyperkalemia, renal disease, anuria. Exacerbated by the effects of
the drug.
o Pregnancy, lactation. Can cause potential adverse effects to the fetus
and baby. Routine use of this drug in pregnancy is not appropriate and
should be used only when there is underlying pathological conditions.
For lactating women, an alternative method of feeding should be
instituted.
Drug interactions
o Salicylates: decreased diuretic effect
o
Side/adverse effects
o CNS: lethargy, confusion, ataxia
o CV: arrhythmias
o Musculoskeletal: muscle cramps
o GU: hyperkalemia, increased loss of bicarbonate (can lead to metabolic
acidosis)
o Associated with various androgen effects such as hirsutism,
gynecomastia, deepening of the voice, and irregular menses.
amiloride Midamor
triamterene Dyrenium