Furosemide Uses, Dosage, Side Effects & Warnings | DrugsAtlas
Authoritative Clinical Reference
Navigation
Subclass
Loop diuretic
Speciality
Nephrology
Schedule (India)
Schedule H
Routes
Oral, Intravenous, Intramuscular
Formulations
- Tablets: 20 mg, 40 mg
- Oral solution: 10 mg/mL (limited to select hospital settings)
- Injection: 10 mg/mL (2 mL ampoule = 20 mg; 4 mL ampoule = 40 mg)
Adult indications
INDICATIONS + DOSING β FOR CLINICIAN USE ONLY
Primary Indications (Approved / Standard in India)
1. Congestive Heart Failure (CHF) β Volume Overload / Pulmonary Congestion
| Parameter | Oral | Intravenous |
|---|---|---|
|
Starting dose
|
20β40 mg once daily | 20β40 mg slow IV push (over 1β2 min) |
|
Titration
|
Increase by 20β40 mg every 6β8 hours based on response | Repeat dose in 2 hours if inadequate response |
|
Usual maintenance
|
40β80 mg/day (single or divided doses) | Convert to oral once stable |
|
Maximum dose
|
600 mg/day (divided doses) | 200 mg/bolus; higher only under specialist care |
Clinical Notes:
- Monitor daily weight, fluid balance, serum electrolytes, BP
- Consider potassium supplementation or combine with spironolactone if hypokalaemia develops
2. Acute Pulmonary Oedema
| Step | Action |
|---|---|
|
Starting dose
|
IV 40 mg bolus (slow push over 1β2 min) |
|
Titration
|
May repeat 40β80 mg IV in 1β2 hours if response inadequate |
|
If already on oral loop diuretic
|
Give IV dose equivalent to patient's total daily oral dose |
|
Maximum dose
|
200 mg per bolus; higher doses require ECG and electrolyte monitoring |
Clinical Notes:
- Administer with oxygen and positioning
- Rapid infusion increases ototoxicity risk
3. Chronic Kidney Disease with Volume Overload
| Parameter | Recommendation |
|---|---|
|
Starting dose
|
40β80 mg oral once or twice daily |
|
Titration
|
Increase to 80β160 mg twice daily based on clinical response |
|
Usual maintenance
|
80β320 mg/day in divided doses |
|
Maximum dose
|
600 mg/day oral (divided) |
Clinical Notes:
- Higher doses often required due to reduced tubular secretion in low GFR
- Consider adding thiazide-type diuretic for sequential nephron blockade in resistant oedema
4. Hypertension (Volume-dependent or Resistant)
| Parameter | Recommendation |
|---|---|
|
Starting dose
|
20 mg once or twice daily |
|
Titration
|
Increase to 40 mg twice daily if needed |
|
Usual maintenance
|
20β80 mg/day |
|
Maximum dose
|
80 mg/day (as adjunct therapy) |
Clinical Notes:
- Not first-line antihypertensive
- Reserve for patients with concurrent fluid overload or CKD
Secondary Indications β Adults Only (Off-label)
| Indication | Dose | Duration | Notes |
|---|---|---|---|
|
Acute Hypercalcaemiaβ OFF-LABEL
|
20β40 mg IV every 2β4 hours | Until calcium normalises | Administer with IV saline; specialist supervision essential; monitor calcium and fluid balance. Based on Indian nephrology practice. |
|
Ascites in Cirrhosis (spironolactone-resistant) β OFF-LABEL
|
20β40 mg oral daily; titrate as needed | Long-term maintenance | Combine with spironolactone (40:100 mg ratio preferred). Monitor for encephalopathy and electrolyte disturbance. Based on Indian hepatology protocols. |
INDICATIONS + DOSING β FOR CLINICIAN USE ONLY
Primary Indications (Approved / Standard in India)
1. Congestive Heart Failure (CHF) β Volume Overload / Pulmonary Congestion
| Parameter | Oral | Intravenous |
|---|---|---|
|
Starting dose
|
20β40 mg once daily | 20β40 mg slow IV push (over 1β2 min) |
|
Titration
|
Increase by 20β40 mg every 6β8 hours based on response | Repeat dose in 2 hours if inadequate response |
|
Usual maintenance
|
40β80 mg/day (single or divided doses) | Convert to oral once stable |
|
Maximum dose
|
600 mg/day (divided doses) | 200 mg/bolus; higher only under specialist care |
Clinical Notes:
- Monitor daily weight, fluid balance, serum electrolytes, BP
- Consider potassium supplementation or combine with spironolactone if hypokalaemia develops
2. Acute Pulmonary Oedema
| Step | Action |
|---|---|
|
Starting dose
|
IV 40 mg bolus (slow push over 1β2 min) |
|
Titration
|
May repeat 40β80 mg IV in 1β2 hours if response inadequate |
|
If already on oral loop diuretic
|
Give IV dose equivalent to patient's total daily oral dose |
|
Maximum dose
|
200 mg per bolus; higher doses require ECG and electrolyte monitoring |
Clinical Notes:
- Administer with oxygen and positioning
- Rapid infusion increases ototoxicity risk
3. Chronic Kidney Disease with Volume Overload
| Parameter | Recommendation |
|---|---|
|
Starting dose
|
40β80 mg oral once or twice daily |
|
Titration
|
Increase to 80β160 mg twice daily based on clinical response |
|
Usual maintenance
|
80β320 mg/day in divided doses |
|
Maximum dose
|
600 mg/day oral (divided) |
Clinical Notes:
- Higher doses often required due to reduced tubular secretion in low GFR
- Consider adding thiazide-type diuretic for sequential nephron blockade in resistant oedema
4. Hypertension (Volume-dependent or Resistant)
| Parameter | Recommendation |
|---|---|
|
Starting dose
|
20 mg once or twice daily |
|
Titration
|
Increase to 40 mg twice daily if needed |
|
Usual maintenance
|
20β80 mg/day |
|
Maximum dose
|
80 mg/day (as adjunct therapy) |
Clinical Notes:
- Not first-line antihypertensive
- Reserve for patients with concurrent fluid overload or CKD
Secondary Indications β Adults Only (Off-label)
| Indication | Dose | Duration | Notes |
|---|---|---|---|
|
Acute Hypercalcaemiaβ OFF-LABEL
|
20β40 mg IV every 2β4 hours | Until calcium normalises | Administer with IV saline; specialist supervision essential; monitor calcium and fluid balance. Based on Indian nephrology practice. |
|
Ascites in Cirrhosis (spironolactone-resistant) β OFF-LABEL
|
20β40 mg oral daily; titrate as needed | Long-term maintenance | Combine with spironolactone (40:100 mg ratio preferred). Monitor for encephalopathy and electrolyte disturbance. Based on Indian hepatology protocols. |
Paediatric indications
PAEDIATRIC DOSING (Specialist Only)
Primary Indications
1. Oedema (Cardiac / Renal / Hepatic Causes)
| Age Group | Route | Starting Dose | Frequency | Maximum Single Dose |
|---|---|---|---|---|
| Neonates (term) | IV or Oral | 0.5β1 mg/kg | Every 12β24 hours | 2 mg/kg |
| Infants (1 month β 1 year) | IV or Oral | 1β2 mg/kg | Every 6β12 hours | 4 mg/kg |
| Children (1β12 years) | IV or Oral | 1β2 mg/kg | Every 6β8 hours | 6 mg/kg (max 40 mg/dose) |
| Adolescents (>12 years) | IV or Oral | 20β40 mg | Once or twice daily | 80 mg/dose |
Safety Monitoring:
- Serum electrolytes (KβΊ, NaβΊ, Ca²βΊ, Mg²βΊ)
- Fluid balance, daily weight
- Audiometry if repeated high-dose IV use
Cautions:
- Avoid in premature neonates unless essential β increased ototoxicity and nephrocalcinosis risk
2. Acute Kidney Injury (Oliguric Phase) β Nephrologist Only
| Parameter | Recommendation |
|---|---|
|
Starting dose
|
1β2 mg/kg IV |
|
Titration
|
May increase to 4 mg/kg if no response |
|
Maximum dose
|
6 mg/kg/dose (specialist discretion) |
Clinical Notes:
- Response-based dosing; not for routine use
- Close monitoring of urine output and electrolytes mandatory
Secondary Indications β Paediatric (Off-label)
| Indication | Dose | Duration | Notes |
|---|---|---|---|
|
Bronchopulmonary Dysplasia (BPD) β OFF-LABEL
|
1 mg/kg/dose oral or IV, once or twice daily | Short-term (days to weeks) | Specialist (neonatologist) only. Limited to NICU settings. Risk of electrolyte imbalance. Based on tertiary NICU protocols in India. |
Age Restriction: Not recommended below 4 weeks of age except under specialist supervision.
Renal Adjustments
| Renal Status | Recommendation |
|---|---|
| MildβModerate impairment (eGFR 15β60) | No dose reduction; may need higher doses due to reduced efficacy |
| Severe impairment (eGFR <15) | Higher doses often required; monitor volume and electrolytes closely |
| Dialysis patients | Can be used for residual diuresis; not removed by haemodialysis |
Note: Avoid dehydration. Combine with thiazide for synergy in resistant cases.
Hepatic adjustment
Contraindications
- Anuria unresponsive to fluid challenge
- Severe hypovolaemia or dehydration
- Known hypersensitivity to furosemide or sulfonamides
- Severe uncorrected hypokalaemia or hyponatraemia
- Hepatic coma or pre-coma (unless under specialist supervision)
Cautions
- Gout or hyperuricaemia (may precipitate acute attack)
- Diabetes mellitus (may worsen glycaemic control)
- Prostatic hypertrophy / bladder outlet obstruction
- Pre-existing hearing impairment
- Concurrent nephrotoxic or ototoxic drug use
- Elderly patients (increased risk of falls, hypotension)
- Severe electrolyte disturbances
Pregnancy
| Parameter | Information |
|---|---|
|
Risk category
|
Use only if benefit clearly outweighs risk |
|
Concerns
|
May reduce placental perfusion; risk of oligohydramnios, fetal electrolyte imbalance |
|
Preferred alternatives
|
Methyldopa, labetalol for hypertension in pregnancy |
|
When to use
|
Only if volume overload poses immediate maternal risk |
|
Monitoring
|
Fetal growth (serial USG), maternal electrolytes, BP |
Lactation
| Parameter | Information |
|---|---|
|
Compatibility
|
Generally compatible with breastfeeding |
|
Milk levels
|
Low; minimal infant exposure expected |
|
Concerns
|
High doses may reduce milk production |
|
Monitoring in infant
|
Weight gain, feeding adequacy, hydration status |
|
Preferred alternatives
|
None specifically preferred; continue if clinically indicated |
Elderly
| Parameter | Recommendation |
|---|---|
|
Starting dose
|
20 mg once daily (lower end of range) |
|
Titration
|
Slow; increase cautiously based on response |
|
Special risks
|
Orthostatic hypotension, falls, hyponatraemia, dehydration, acute kidney injury |
|
Monitoring
|
BP (including postural), renal function, electrolytes at baseline and periodically |
Major drug interactions
| Drug | Interaction | Management |
|---|---|---|
|
Aminoglycosides(gentamicin, amikacin)
|
Additive ototoxicity and nephrotoxicity, especially with IV furosemide | Avoid combination if possible; if essential, monitor hearing and renal function |
|
Digoxin
|
Hypokalaemia increases digoxin toxicity risk | Monitor potassium; supplement or add KβΊ-sparing diuretic |
|
Lithium
|
Reduced lithium clearance; increased toxicity risk | Monitor lithium levels closely; dose adjustment may be needed |
|
NSAIDs
|
Reduce diuretic efficacy; increase AKI risk | Avoid routine use; use paracetamol as alternative analgesic |
Moderate drug interactions
| Drug | Interaction | Management |
|---|---|---|
|
Corticosteroids
|
Additive hypokalaemia | Monitor potassium; consider supplementation |
|
Antidiabetic agents
|
May blunt hypoglycaemic effect | Monitor blood glucose; adjust antidiabetic dose if needed |
|
ACE inhibitors / ARBs
|
Additive hypotension, especially first dose | Start at low dose; monitor BP |
|
Proton pump inhibitors
|
Combined risk of hypomagnesaemia | Monitor magnesium in long-term use |
|
Antipsychotics(haloperidol, risperidone)
|
Electrolyte imbalance may prolong QTc | Monitor ECG and electrolytes |
|
Antiepileptics(phenytoin)
|
May reduce furosemide absorption | Monitor diuretic response |
Common Adverse effects
- Hypokalaemia
- Hyponatraemia
- Postural hypotension
- Hyperuricaemia
- Dizziness, fatigue
- Dehydration
- Hyperglycaemia
- Increased urinary frequency
Serious Adverse effects
| Effect | Notes |
|---|---|
|
Ototoxicity
|
Risk increased with rapid IV infusion, high doses, renal impairment, or concurrent aminoglycosides; may be irreversible |
|
Severe electrolyte disturbance
|
Hypokalaemia, hyponatraemia, hypomagnesaemia β can cause arrhythmias |
|
Stevens-Johnson Syndrome / TEN
|
Rare; discontinue immediately if rash develops |
|
Acute pancreatitis
|
Rare; consider if unexplained abdominal pain occurs |
|
Photosensitivity
|
Advise sun protection |
|
Blood dyscrasias
|
Agranulocytosis, thrombocytopenia (rare) |
Monitoring requirements
| Timing | Parameters |
|---|---|
|
Baseline
|
Serum electrolytes (KβΊ, NaβΊ, Mg²βΊ), renal function (creatinine, urea), BP, uric acid |
|
After initiation / dose change
|
Electrolytes and renal function within 1 week |
|
Long-term
|
Electrolytes, renal function, uric acid every 1β3 months |
|
CHF / oedema management
|
Daily weight, fluid balance assessment |
|
High-dose IV or concurrent digoxin
|
ECG monitoring |
|
Paediatric (repeated IV doses)
|
Audiometry |
Brands in India
- Lasix (Sanofi)
- Frusemide (generic β multiple manufacturers)
- Frusenex (Macleods)
- Frusol (Micro Labs)
- Furoped (Ipca)
- Dytor (combination with torsemide β note: different loop diuretic; FDC with spironolactone also available)
Price range (INR)
| Formulation | Approximate Price |
|---|---|
| Tablet 40 mg | βΉ1β3 per tablet |
| Injection 20 mg (2 mL) | βΉ4β8 per ampoule |
| Injection 40 mg (4 mL) | βΉ6β12 per ampoule |
Note: Listed under NLEM 2022; prices regulated by NPPA. Government supply rates may be lower.
Clinical pearls
- IV administration: Always give slow IV push (over 1β2 minutes); rapid injection increases ototoxicity risk.
- Potassium management: Routinely monitor potassium; consider adding spironolactone or potassium chloride supplementation if persistent hypokalaemia.
- Diuretic resistance: In resistant oedema, combine with thiazide (metolazone or hydrochlorothiazide) for sequential nephron blockade β requires close monitoring.
- Avoid NSAIDs: These blunt the diuretic effect and increase AKI risk; use paracetamol for analgesia.
- Metabolic effects: May worsen diabetes control and precipitate gout β monitor glucose and uric acid accordingly.
- IV to oral conversion: Oral bioavailability is approximately 50%; when converting from IV to oral, consider doubling the dose or using more frequent dosing.
Version
RxIndia v1.1 β 05 Jan 2025
Reference
- CDSCO approved prescribing information
- Indian Pharmacopoeia / National Formulary of India
- NLEM 2022
- API Textbook of Medicine
- AIIMS Drug Formulary
- Indian Society of Nephrology Guidelines
- Indian Academy of Pediatrics (IAP) treatment protocols
- Harrison's Principles of Internal Medicine
- Goodman & Gilman's The Pharmacological Basis of Therapeutics
- Tertiary NICU protocols (for paediatric off-label use)
βοΈ
Clinical Responsibility
This platform is designed strictly for healthcare professionals. Data provided is synthesized from authoritative pharmacological sources and clinical registries. Do not use for consumer medical decisions. Always verify critical dosing and contraindications with official institutional protocols and peer-reviewed journals.
Content Feedback
Is this information helpful?
Help us improve our clinical database for the medical community.