Furosemide
Dosage & Administration Guidelines
| Species | Route | Dose | Frequency | Duration & Clinical Notes |
|---|---|---|---|---|
| Dog | PO | 2-5 mg/kg | q8-12h | Duration: Variable; adjust to effect Notes: For chronic heart failure, start at lower end and titrate to lowest effective dose. |
| Dog | IV/IM | 1-2 mg/kg | q1-2h as needed | Duration: Acute management Notes: IV administration for emergencies; monitor hydration and electrolytes. |
| Cat | PO | 1-2 mg/kg | q12-24h | Duration: Variable Notes: Cats are more sensitive; use lower doses. |
| Cat | IV/IM | 0.5-1 mg/kg | q1-2h as needed | Duration: Acute management Notes: Use with caution in cats with renal disease. |
| Horse | IV | 0.5-1 mg/kg | q12-24h | Duration: Variable Notes: For EIPH prophylaxis, administer 4 hours before exercise. |
| Horse | PO | 1-2 mg/kg | q24h | Duration: Variable Notes: Oral bioavailability is lower; adjust dose. |
| Cattle | IV/IM | 0.5-1 mg/kg | q12-24h | Duration: Variable Notes: For udder edema, use 0.5-1 mg/kg IV or IM. |
| Cattle | PO | 1-2 mg/kg | q24h | Duration: Variable Notes: Oral dose may be higher due to lower bioavailability. |
| Small Ruminants | IV/IM | 1-2 mg/kg | q12-24h | Duration: Variable Notes: Use with caution; monitor electrolytes. |
| Rabbit | PO/SC/IM | 1-5 mg/kg | q12-24h | Duration: Variable Notes: Doses up to 5 mg/kg may be used; monitor renal function. |
| Birds/Poultry | IM/PO | 0.1-0.5 mg/kg | q12-24h | Duration: Variable Notes: Limited data; use with caution. |
Clinical Indications & Species Uses
- Diuresis
- Edema of various etiologies
- Hypertension
- Hypercalcemia
- Pulmonary edema (cardiogenic and non-cardiogenic)
- Congestive heart failure (acute and chronic)
- Ascites
- Pleural effusion
- Hypertension
- Acute renal failure (oliguric)
- Hypercalcemia
- Cerebral edema
- Pulmonary edema
- Congestive heart failure
- Pleural effusion
- Ascites
- Hypertension
- Acute renal failure (oliguric)
- Hypercalcemia
- Pulmonary edema
- Exercise-induced pulmonary hemorrhage (EIPH) prophylaxis
- Congestive heart failure
- Edema (e.g., ventral edema)
- Hypercalcemia
- Pulmonary edema
- Congestive heart failure
- Udder edema
- Ascites
- Hypercalcemia
- Pulmonary edema
- Congestive heart failure
- Edema
- Ascites
- Pulmonary edema
- Congestive heart failure
- Ascites
- Edema
- Pulmonary edema
- Ascites
- Edema
- Edema
- Ascites
- Congestive heart failure (in some species)
Pharmacology & Mechanism of Action
Drug Class: Loop Diuretic | Pharmacological Group: Sulfonamide derivative
Mechanism of Action: Furosemide inhibits the Na+-K+-2Cl- symporter (NKCC2) in the thick ascending limb of the loop of Henle, reducing reabsorption of sodium and chloride, leading to increased excretion of water, sodium, chloride, potassium, calcium, and magnesium. It also stimulates renal prostaglandin synthesis, causing renal vasodilation and increased renal blood flow.
Pharmacodynamics: Furosemide produces a rapid and profound diuresis, with onset of action within minutes after IV administration and within 30-60 minutes after oral administration. It reduces extracellular fluid volume, decreases preload and afterload, and lowers blood pressure. It also reduces pulmonary capillary wedge pressure and pulmonary edema. Chronic use can lead to electrolyte imbalances and activation of the renin-angiotensin-aldosterone system.
β‘ Pharmacokinetics Summary
Available Formulations & Strengths
Contraindications & Clinical Warnings
- Hypersensitivity to furosemide or sulfonamides
- Anuria or severe renal failure with no urine output
- Severe electrolyte depletion (e.g., hypokalemia, hyponatremia)
- Hypovolemia or dehydration
- Hepatic coma or pre-coma
- Concurrent use of other ototoxic drugs (e.g., aminoglycosides) may increase risk of ototoxicity
- Use with caution in animals with hepatic cirrhosis, diabetes mellitus, or gout (hyperuricemia).
- Monitor renal function, electrolytes (especially potassium, sodium, chloride), and hydration status during therapy.
- May cause dehydration and electrolyte imbalances; ensure adequate water intake.
- In animals with pre-existing renal disease, use lower doses and monitor closely.
- May cause ototoxicity, especially with rapid IV administration or high doses.
- In horses, use with caution in animals with electrolyte imbalances; may affect performance.
- In food animals, observe withdrawal times.
- Use in pregnant animals only if clearly needed; furosemide crosses the placenta.
Adverse Effects & Reactions
Common:
- Increased urination
- Electrolyte imbalances (hypokalemia, hyponatremia, hypochloremia)
- Dehydration
- Gastrointestinal upset (vomiting, diarrhea)
- Weakness
- Lethargy
Serious / Severe:
- Ototoxicity (especially with rapid IV administration)
- Renal dysfunction or failure
- Cardiac arrhythmias (due to electrolyte disturbances)
- Hypotension
- Pancreatitis (rare)
- Blood dyscrasias (rare)
Rare:
- Allergic reactions (skin rash, anaphylaxis)
- Bone marrow suppression
- Hyperglycemia
- Hyperuricemia
- Calcium oxalate urolithiasis
Key Drug Interactions
| Interacting Drug / Class | Clinical Effect & Mechanism | Severity |
|---|---|---|
| Aminoglycosides (e.g., gentamicin) | Increased risk of ototoxicity and nephrotoxicity | High |
| Corticosteroids | Increased risk of hypokalemia | Moderate |
| Digoxin | Increased risk of digoxin toxicity due to hypokalemia | High |
| NSAIDs (e.g., flunixin, carprofen) | Reduced diuretic effect and increased risk of nephrotoxicity | Moderate |
| ACE inhibitors (e.g., enalapril) | Additive hypotensive effect; risk of hyperkalemia if potassium-sparing diuretics are used | Moderate |
| Lithium | Increased lithium levels and toxicity | High |
| Suxamethonium (succinylcholine) | Prolonged neuromuscular blockade | Moderate |
Overdose & Toxicity Management
Signs of Toxicity:
- Severe dehydration
- Hypotension
- Electrolyte depletion (hypokalemia, hyponatremia, hypochloremia)
- Metabolic alkalosis
- Cardiac arrhythmias
- Weakness, collapse
- Renal failure
- Ototoxicity (deafness)
Emergency Treatment Protocol: Discontinue the drug. Provide supportive care: fluid and electrolyte replacement (IV fluids with appropriate electrolytes), monitoring of vital signs and ECG. In severe cases, consider hemodialysis or peritoneal dialysis. There is no specific antidote.
Food Animal Withdrawal Times
Withdrawal times may vary by country and formulation; consult local regulations. In the US, furosemide is not approved for food animals, but extra-label use requires extended withdrawal periods (e.g., 30 days for meat, 7 days for milk) as per FARAD guidelines.
Storage, Handling & Regulatory Information
Storage Temperature: Store at controlled room temperature (20-25Β°C, excursions permitted to 15-30Β°C).
Light Sensitivity: Light-sensitive β protect from direct exposure.
Handling & Special Conditions: Protect from light and moisture. Keep in a tightly closed container.
Dispensing Status: Prescription Required (Rx Only)
Approval Status: Approved for veterinary use in dogs, cats, and horses (e.g., Lasix).
Extra-Label (Off-Label) Use: In the US, furosemide is approved for use in dogs, cats, and horses. Extra-label use in food animals is permitted under AMDUCA with veterinary oversight, but requires extended withdrawal times. In the EU, similar regulations apply.
Clinical Pearls & Practice Notes
References & Literature
- π Plumb's Veterinary Drug Handbook
- π Papich Veterinary Pharmacology and Therapeutics
- π Compendium of Veterinary Products (CVP)