What is the oral to intravenous (IV) dose equivalence for furosemide (Lasix)?

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Last updated: December 26, 2025View editorial policy

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Oral to IV Furosemide Dose Equivalence

Oral and IV furosemide are considered approximately 1:1 equivalent in dose, meaning 40 mg oral equals 40 mg IV, though oral bioavailability averages only 40-50% in most patients.

Bioavailability and Route Selection

The oral bioavailability of furosemide is approximately 40-50% in typical patients 1. However, in cirrhotic patients specifically, oral furosemide demonstrates good bioavailability and is actually preferred over IV administration because IV dosing causes acute reductions in glomerular filtration rate 2, 3. This represents an important exception to typical pharmacokinetic assumptions.

Despite the reduced oral bioavailability in non-cirrhotic patients, clinical dosing guidelines consistently use a 1:1 conversion ratio between oral and IV routes 3, 4. For example:

  • Standard starting dose: 40 mg oral = 40 mg IV 2, 3
  • Maximum dose in cirrhosis: 160 mg/day oral = 160 mg/day IV 3
  • Acute heart failure dosing: patients on 40 mg oral at home should receive at least 40 mg IV when hospitalized 4

Clinical Dosing Principles

When converting from oral to IV in acute settings, the IV dose should equal or exceed the home oral dose to ensure adequate diuretic response 4. This is because:

  • Gut wall edema in heart failure reduces oral absorption further, making IV more reliable 3
  • The first dose produces maximal effect, with subsequent doses showing up to 25% less efficacy 3
  • Inadequate initial IV dosing in chronic diuretic users leads to delayed decongestion 4

For acute heart failure, guidelines recommend starting with 20-40 mg IV bolus, but patients already taking >40 mg oral daily should receive 80 mg IV rather than 40 mg IV 3, 4.

Disease-Specific Considerations

In cirrhosis with ascites, oral administration is explicitly preferred when the patient can tolerate oral intake 2, 3. The typical regimen is furosemide 40 mg oral combined with spironolactone 100 mg as a single morning dose, with maximum furosemide dose of 160 mg/day 2, 3.

In acute decompensated heart failure or pulmonary edema, IV administration is preferred for rapid onset and reliable absorption 3, 4. Initial dosing is 20-40 mg IV bolus over 1-2 minutes, followed by continuous infusion at 3 mg/hour if needed, with maximum infusion rate of 24 mg/hour 4.

Important Caveats

The 1:1 dosing equivalence used in clinical practice does not reflect true pharmacokinetic equivalence, as oral bioavailability is only 40-50% 1. However, this dosing convention has been validated in clinical trials and guideline recommendations 2, 3, 4. The discrepancy likely reflects that the therapeutic window is wide enough to accommodate this simplified dosing approach while maintaining safety and efficacy.

Peak diuretic effect occurs within 1-1.5 hours after oral administration and faster with IV dosing 3. When switching routes, monitor urine output targeting >0.5 mL/kg/hour and adjust doses based on clinical response rather than strict pharmacokinetic calculations 3, 4.

References

Research

Bumetanide and furosemide.

Clinical pharmacology and therapeutics, 1983

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Furosemide Administration Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Furosemide Administration in Acute Heart Failure

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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