Furosemide (Lasix)

Diureticprescriptionoral · inferred

Loop diuretic that inhibits sodium-potassium-chloride co-transporter in the thick ascending limb of the loop of Henle. Rapidly absorbed orally with variable bioavailability (10-100%). Eliminated ~65% unchanged renally via active secretion; ~35% metabolized. Used for edema, heart failure, hypertension. Short plasma half-life but potent diuretic effect. Highly protein-bound (~99%), which may reduce renal excretion in renal failure.

Projected serum levels — 40 mg, once daily

Furosemide (Lasix)
Furosemide (Lasix) modeled serum levels, 40 mg once daily over 15 days Population-based pharmacokinetic estimate. Steady state reached after approximately 1 days. 0 5 10 15 20 Day 0 Day 4 Day 8 Day 11 Day 15 Time on a regular schedule ≈ steady state · day 1

Maintenance schedule: 40 mg once daily (oral).

Modeled steady state after ~1 days: peak ≈ 14.0 mg, trough ≈ 0.006 mg body load. Population-based estimate over 15 days for a 40 mg dose at a 70 kg reference body mass — the interactive app scales curves to your doses, timing, and body mass.

Key facts

Category
Diuretic
Route modeled
Oral
Model confidence
inferred
Half-life
2 h
Common dose
40 mg
Suggested maximum
600 mg/day
Reference dose range
20–600 mg (single dose)
Suggested cadence
once daily
Validated against
40 mg oral — Cmax 1.4 mg/L at 1 h

Documented interactions

  • danger
    CBD (Cannabidiol) + Furosemide (Lasix) CYP inhibition

    CBD (Cannabidiol) reversible_inhibitor of UGT1A9 predicted to change Furosemide (Lasix) AUC by ~3.33x

  • danger
    Levothyroxine (Synthroid) + Furosemide (Lasix) Protein binding

    Furosemide (Lasix) may displace Levothyroxine (Synthroid) from plasma protein binding sites, transiently raising free drug concentration. This drug has a narrow therapeutic index; free concentration…

  • danger
    Tacrolimus (Prograf) + Furosemide (Lasix) Protein binding

    Furosemide (Lasix) may displace Tacrolimus (Prograf) from plasma protein binding sites, transiently raising free drug concentration. This drug has a narrow therapeutic index; free concentration…

  • danger
    Warfarin (Coumadin) + Furosemide (Lasix) Protein binding

    Furosemide (Lasix) may displace Warfarin (Coumadin) from plasma protein binding sites, transiently raising free drug concentration. This drug has a narrow therapeutic index; free concentration…

  • warning
    Apigenin + Furosemide (Lasix) Protein binding

    Apigenin may displace Furosemide (Lasix) from plasma protein binding sites, transiently raising free drug concentration.

  • warning
    Aripiprazole (Abilify) + Furosemide (Lasix) Protein binding

    Furosemide (Lasix) may displace Aripiprazole (Abilify) from plasma protein binding sites, transiently raising free drug concentration.

Serum checks 146 modeled interaction pairings for furosemide (lasix) across your whole stack — absorption conflicts, enzyme inhibition, and nutrient depletion included.

Research behind this entry

  1. Disposition and absolute bioavailability of furosemide in healthy males Dresser GK et al. · Journal of Pharmacology and Experimental Therapeutics, 1984 DOI

    Comprehensive pharmacokinetic study establishing furosemide bioavailability range of 10-100% with high inter-individual variability due to erratic GI absorption and active renal secretion as primary elimination route.

  2. Pharmacokinetics and metabolism of furosemide in man Beermann B et al. · European Journal of Drug Metabolism and Pharmacokinetics, 1976 DOI

    Foundational study demonstrating hepatic metabolism accounts for ~35% of furosemide elimination, with renal excretion of intact drug as primary route. Shows non-linear pharmacokinetics at higher doses.

  3. Diuretic therapy Brater DC · New England Journal of Medicine, 1998 DOI

    Clinical review of diuretic therapy mechanisms and clinical pharmacology, discussing furosemide as the most frequently prescribed loop diuretic with well-understood effects on renal hemodynamics and electrolyte…

3 published studies referenced in the app, each with a plain-language summary.