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Drug reference

Mannitol

Osmotic diuretic · Diuretic, Antiglaucoma agent, Agent for cerebral edema

Also known as D-Mannitol, Osmotic Diuretic Solution

START
Raised ICP: 0.25–1 g/kg IV 20% over 15–30 min; oliguria test dose 0.2 g/kg
TYPICAL MAX
~2 g/kg/day; keep osmolality <320 mOsm/kg
STOP IF
No urine response to test dose, osmolar gap/osmolality excessive, fluid overload/pulmonary oedema
WATCH
Serum osmolality + osmolar gap, renal function, electrolytes, fluid balance, neuro status
CDSCO approvedSchedule HJan AushadhiNPPA price-controlledATC B05BC01
Dose laddermg/d
12.5kstart35ktitrate70kmax140kceiling
Renal dose adjustmenteGFR mL/min/1.73m²
CAUTIONUse with osmolality monitoring30REDUCETest dose only; discontinue if no di…90

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
30minONSET1hPEAK1.4h6hDURATION
ONSET
30min · ICP/diuresis onset
PEAK
1h · peak osmotic effect
1.4h · plasma t½
DURATION
6h · effect duration
EXCRETION
Renal, rapidly filtered, largely unchanged
route + CYP
INTERACTIONS
11 major
SEVERE in our sources
PREGNANCY
Use only if clearly needed for serious indications — limited data
FDA category + note
Top interactionssee all 12
  • AmikacinSevereDatabaseDDInter
  • DigoxinSevereDatabaseKimi deep-research + Cla
  • DroperidolSevereDatabaseDDInter
  • GentamicinSevereDatabaseDDInter
Available in India

8 branded formulations and 32 fixed-dose combinations. Look up specific brands in the Drugs workspace.

Jan Aushadhi — generic available at GoI pharmacies

Mechanism

Freely filtered, non-reabsorbed sugar alcohol that raises plasma and tubular osmolality — extracts water from tissues (brain, eye) into the intravascular space and induces osmotic diuresis with obligatory water and electrolyte loss.

Indications

Raised intracranial pressure / cerebral oedemaAcute glaucoma / pre-ophthalmic-surgery IOP reductionPromotion of diuresis in oliguria / forced diuresis for toxinsGenitourinary irrigation (TURP)

Dosing

Adult
Raised ICP: 0.25–1 g/kg IV (20% solution) over 15–30 min, repeat per osmolality/response. Oliguria test dose 0.2 g/kg over 3–5 min.
Pediatric
0.25–1 g/kg IV (specialist).
Renal adjustment
Test dose required; do not continue if no urine response (risk of fluid overload).
Hepatic adjustment
No specific adjustment.
Geriatric
Cautious; monitor volume/cardiac status.
Max dose
Up to ~2 g/kg/day; keep serum osmolality <320 mOsm/kg

Pharmacokinetics

Onset
Diuresis 1–3 h; ICP reduction within 15–30 min
Peak effect
~1 h (osmotic effect)
Duration
~3–8 h
Half-life
~1.1–1.6 h (longer in renal failure)
Bioavailability
IV (negligible oral)
Protein binding
Negligible
Metabolism
Minimal (small fraction hepatic to glycogen)
Excretion
Renal — rapidly filtered, largely unchanged

Contraindications

  • Anuria due to severe renal disease (not responsive)
  • Severe established pulmonary oedema / congestive heart failure
  • Active intracranial bleeding (except during craniotomy)
  • Severe dehydration
  • Progressive renal failure/oliguria after a test dose

Side effects

Common
PolyuriaThirst/dehydrationHeadacheNauseaElectrolyte disturbance
Serious
  • Acute kidney injury (high cumulative dose, osmotic nephrosis)
  • Pulmonary oedema / fluid overload (initial volume expansion)
  • Severe electrolyte/osmolar disturbance, rebound ICP rise
  • Extravasation tissue injury

Pregnancy & lactation

Pregnancy

Use only if clearly needed for serious indications — limited data

Lactation

Limited data; short-term acute use — caution

Drug interactions

Amikacin
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Digoxin
Severe
Database

Mannitol-induced hypokalaemia potentiates digoxin toxicity

Monitor K+ and digoxin levels

Source: Kimi deep-research + Cla

Droperidol
Severe
Database

Clinical effect not specified

Source: DDInter

Gentamicin
Severe
Database

.

Source: DDInter

Kanamycin
Severe
Database

Clinical effect not specified

Source: DDInter

Neomycin
Severe
Database

Clinical effect not specified

Source: DDInter

Nephrotoxic Drugs
Severe
Database

Additive renal injury (osmotic nephrosis)

Avoid; monitor renal function/osmolality

Source: Kimi deep-research + Cla

Netilmicin
Severe
Database

Clinical effect not specified

Source: DDInter

Plazomicin
Severe
Database

Clinical effect not specified

Source: DDInter

Streptomycin
Severe
Database

Clinical effect not specified

Source: DDInter

Tobramycin
Severe
Database

Clinical effect not specified

Source: DDInter

Lithium
Moderate
Database

Altered lithium excretion

Monitor lithium levels

Source: Kimi deep-research + Cla

Related guidelines

Ask House about Mannitol

Continue into a citation-backed clinical answer with the drug context already attached.

Sources: KD Tripathi 7e, Goodman & Gilman 14e, Harrison 22e, Katzung·Verified: 2026-05-19 · House clinical team·Cockpit curated: 2026-05-19