Indications
Edema due to heart failure, hepatic impairment, or renal
disease. Hypertension.
Action
Inhibits the reabsorption of sodium and chloride from
the loop of Henle and distal renal tubule. Increases renal
excretion of water, sodium, chloride, magnesium,
potassium, and calcium. Effectiveness persists in impaired
renal function. Therapeutic Effects: Diuresis
and subsequent mobilization of excess fluid (edema,
pleural effusions). Decreased BP.
Pharmacokinetics
Absorption: 60–67% absorbed after oral administration
(pin acute HF and in renal failure); also absorbed
from IM sites.
Distribution: Crosses placenta, enters breast milk.
Protein Binding: 91–99%.
Metabolism and Excretion: Minimally metabolized
by liver, some nonhepatic metabolism, some renal
excretion as unchanged drug.
Half-life: 30–60 min (qin renal impairment).
TIME/ACTION PROFILE (diuretic effect)
ROUTE ONSET PEAK DURATION
PO 30–60 min 1–2 hr 6–8 hr
IM 10–30 min unknown 4–8 hr
IV 5 min 30 min 2 hr
Contraindications/Precautions
Contraindicated in: Hypersensitivity; Cross-sensitivity
with thiazides and sulfonamides may occur; Hepatic
coma or anuria; Some liquid products may contain
alcohol, avoid in patients with alcohol intolerance.
Use Cautiously in: Severe liver disease (may precipitate
hepatic coma; concurrent use with potassiumsparing
diuretics may be necessary); Electrolyte depletion;
Diabetes mellitus; Hypoproteinemia (qrisk of
ototoxicity); Severe renal impairment (qrisk of ototoxicity);
OB, Lactation: Safety not established; Pedi:qrisk
for renal calculi and patent ductus arteriosis in premature
neonates; Geri: May haveqrisk of side effects, especially
hypotension and electrolyte imbalance, at usual
doses.
Adverse Reactions/Side Effects
CNS: blurred vision, dizziness, headache, vertigo.
EENT: hearing loss, tinnitus. CV: hypotension. GI:
anorexia, constipation, diarrhea, dry mouth, dyspepsia,
qliver enzymes, nausea, pancreatitis, vomiting. GU:q
BUN, excessive urination, nephrocalcinosis. Derm:
ERYTHEMA MULTIFORME, STEVENS-JOHNSON SYNDROME,
TOXIC EPIDERMAL NECROLYSIS, photosensitivity, pruritis,
rash, urticaria. Endo: hypercholesterolemia, hyperglycemia,
hypertriglyceridemia, hyperuricemia. F and E:
dehydration, hypocalcemia, hypochloremia, hypokalemia,
hypomagnesemia, hyponatremia, hypovolemia,
metabolic alkalosis. Hemat: APLASTIC ANEMIA, AGRANULOCYTOSIS,
hemolytic anemia, leukopenia, thrombocytopenia.
MS: muscle cramps. Neuro: paresthesia.
Misc: fever.
Interactions
Drug-Drug:qrisk of hypotension with antihypertensives,
nitrates, or acute ingestion of alcohol.
qrisk of hypokalemia with other diuretics, amphotericin
B, stimulant laxatives, and
corticosteroids. Hypokalemia mayqrisk of digoxin
toxicity andqrisk of arrhythmia in patients taking
drugs that prolong the QT interval.plithium excretion,
may cause lithium toxicity.qrisk of ototoxicity with aminoglycosides or cisplatin.qrisk of nephrotoxicity
with cisplatin. NSAIDSpeffects of furosemide.
Mayqrisk of methotrexate toxicity.peffects of
furosemide when given at same time as sucralfate,
cholestyramine, or colestipol.qrisk of salicylate
toxicity (with use of high-dose salicylate therapy).
Concurrent use with cyclosporine mayqrisk of gouty
arthritis.
Route/Dosage
Edema
PO (Adults): 20–80 mg/day as a single dose initially,
may repeat in 6–8 hr; mayqdose by 20–40 mg q 6–8
hr until desired response. Maintenance doses may be
given once or twice daily (doses up to 2.5 g/day have
been used in patients with HF or renal disease). Hypertension—
40 twice daily initially (when added to regimen,
pdose of other antihypertensives by 50%); adjust
further dosing based on response; Hypercalcemia—
120 mg/day in 1–3 doses.
PO (Children 1 mo): 2 mg/kg as a single dose; may
beqby 1–2 mg/kg q 6–8 hr (maximum dose6
mg/kg).
PO (Neonates): 1–4 mg/kg/dose 1–2 times/day.
IM, IV (Adults): 20–40 mg, may repeat in 1–2 hr
andqby 20 mg every 1–2 hr until response is obtained,
maintenance dose may be given q 6–12 hr;
Continuous infusion—Bolus 0.1 mg/kg followed by
0.1 mg/kg/hr, double q 2 hr to a maximum of 0.4 mg/
kg/hr.
IM, IV (Children): 1–2 mg/kg/dose q 6–12 hr; Continuous
infusion—0.05 mg/kg/hr, titrate to clinical
effect.
IM, IV (Neonates): 1–2 mg/kg/dose q 12–24 hr.
Hypertension
PO (Adults): 40 twice daily initially (when added to
regimen,pdose of other antihypertensives by 50%);
adjust further dosing based on response.
Availability (generic available)
Tablets: 20 mg, 40 mg, 80 mg, 500 mg. Cost: Generic—
20 mg $6.50/100, 40 mg $7.11/100, 80 mg
$10.83/100. Oral solution (10 mg/mL—orange
flavor, 8 mg/mL—pineapple—peach flavor): 8
mg/mL, 10 mg/mL. Cost: Generic—10 mg/mL
$10.40/60 mL. Solution for injection: 10 mg/mL.
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