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Diuretic · Osmotic Diuretic

Mannitol (Mannitol)

Also sold as: Mannitol BP, Osmofundin, Manitol

Pregnancy

Cat C

Lactation

Unknown

Schedule

H

Forms

IV infusion solution (10% — 100g/L; 15% — 150g/L; 20% — 200g/L; 25% — 250g/L)

Indications

Adult Dosing

Raised intracranial pressure (cerebral oedema)

0.25–2g/kg IV (20% solution)

Over 30–60 minutes; may repeat every 6–8 hours as needed; maximum 48–72 hours continuous use

Target serum osmolality 300–320 mOsm/kg; STOP if osmolality >320 mOsm/kg (risk of rebound oedema and renal failure); place urinary catheter to measure output; keep head of bed at 30°; monitor ICP if available

Acute angle-closure glaucoma / raised intraocular pressure

1.5–2g/kg IV (20% solution)

Over 30–60 minutes; single dose or repeat once after 4–6 hours

Rapid IOP reduction within 30–60 minutes; definitive treatment (iridotomy) should follow

Oliguric acute renal failure (prevention)

50–100g IV

Over 30–90 minutes; single dose (prophylaxis)

Used pre- or peri-operatively in high-risk cases (aortic surgery, liver transplant, rhabdomyolysis, haemolysis); no evidence of benefit in established AKI

Forced diuresis (drug overdose)

50–200g IV

Over 24 hours at 5–10g/hour; monitor urine output and osmolality

Effective for drugs cleared by renal excretion (salicylates — alkaline diuresis added; barbiturates); maintain urine output >100mL/hour; ensure adequate pre-hydration

Maximum daily dose: 200g/day (raised ICP); 200g/24h (forced diuresis); guided by serum osmolality

Pediatric Dosing

Age Range: All ages (neonates under specialist care only)
Dose: 0.25–1g/kg per dose (raised ICP)
Max/day: As per clinical response; limit to prevent hyperosmolality

Head trauma/ICP: 0.5–1g/kg IV over 15–30 minutes; monitor osmolality; avoid in neonates unless life-threatening; hypertonic solutions require central or large peripheral line

Calculate exact mL by weight →

Renal Dose Adjustment

CrCl / eGFRDose Adjustment
Oliguria / acute renal failureCONTRAINDICATED in established anuria — no mechanism of action; mannitol will accumulate, causing volume overload, pulmonary oedema, and hyperosmolality
Mild-moderate CKDUse with great caution; monitor osmolality and renal function closely; accumulation risk
Calculate eGFR / CrCl →

Hepatic Adjustment

No hepatic metabolism; excreted unchanged by kidneys. Hepatic failure per se does not alter dosing but coexisting renal impairment (hepatorenal syndrome) is a contraindication.

Pregnancy & Lactation

Pregnancy: Category C

Limited data. Crosses placenta — osmotic load may cause fetal dehydration. Use only for life-threatening maternal indications (e.g. severe raised ICP). Monitor fetal wellbeing.

Lactation: Unknown

No data available. Given that mannitol is used only for acute hospital indications, breastfeeding is typically not an active concern during treatment. Discard milk during IV treatment.

Top Drug Interactions

Interacting DrugEffectSeverity
CyclosporineMannitol increases cyclosporine nephrotoxicity (osmotic tubular damage combined with calcineurin inhibitor nephrotoxicity); monitor renal function closelyMajor
LithiumMannitol increases renal lithium excretion — reduces lithium levels; may be used therapeutically in lithium toxicity but monitor lithium levelsModerate
DigoxinMannitol-induced electrolyte shifts (hypokalemia, hyponatraemia) can alter digoxin sensitivity and toxicity risk; monitor electrolytesModerate
AminoglycosidesAdditive nephrotoxicity; combined osmotic and tubular toxicity; use with caution and monitor renal functionModerate
Blood productsDO NOT mix mannitol with blood — causes pseudoagglutination (red cell clumping); administer through separate IV lineMajor

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Side Effects

Common

  • Headache (from fluid shifts)
  • Nausea and vomiting
  • Dry mouth and thirst
  • Dizziness
  • Chills and fever (during infusion)
  • Polyuria (during and after infusion)
  • Electrolyte disturbances (hyponatraemia, hypokalaemia)

Serious / Discontinue If

  • Acute pulmonary oedema (rapid volume expansion — especially with cardiac compromise or if anuric)
  • Severe hyperosmolality (serum osmolality >320 mOsm/kg) — can cause renal tubular necrosis
  • Rebound intracranial hypertension (after prolonged use — damaged BBB allows mannitol to accumulate in brain)
  • Severe hyponatraemia (paradoxical — dilutional)
  • Acute kidney injury (osmotic nephrosis) with prolonged high-dose use
  • Extravasation leading to tissue necrosis (hypertonic solution)
  • Electrolyte-related cardiac arrhythmias

Contraindications

Available Indian Brands

BrandManufacturerPrice (approx)
Mannitol 20% 250mLBaxter₹125/bottle
Osmofundin 15% 250mLB.Braun₹145/bottle

Monitoring Required

Patient Counseling Points

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Clinically reviewed by: Dr. Suresh Babu, MD (Medicine), DM (Neurology), MCh (Neurosurgery collaboration), NIMHANS Bangalore

Last reviewed: 2026-04-10

References

  • Carney N et al. Guidelines for the Management of Severe Traumatic Brain Injury, 4th Edition. Neurosurgery 2017;80(1):6–15.
  • Wakai A et al. Mannitol for acute traumatic brain injury. Cochrane Database Syst Rev 2013.
  • Ropper AH. Hyperosmolar therapy for raised intracranial pressure. NEJM 2012;367(8):746–752.
  • BNF 86 (2024). Mannitol monograph.
  • CIMS India Drug Reference 2024. Mannitol monograph.
  • Staykov D et al. Mannitol and hypertonic saline in the treatment of cerebral oedema. J Neurol Sci 2011.
Disclaimer: This information is for clinical reference only. It is not exhaustive and does not substitute clinical judgement. Always verify current dosing against the manufacturer's prescribing information and current treatment guidelines. Drug prices are approximate and may vary.