Product image of Mannitol Lavoisier (Mannitol) supplied by GNH India

Mannitol Lavoisier

Active Ingredient:
Mannitol
Origin:
EU

Mannitol Lavoisier (Mannitol)

Mannitol, the active ingredient in Mannitol Lavoisier, is an osmotic diuretic presented as a sterile intravenous solution for parenteral use. It is employed to lower intracranial pressure, facilitate diuresis in acute renal failure, and manage fluid balance in critical care patients.

GNH India supplies Mannitol Lavoisier as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory documentation for import across EU and other markets.

Manufacturer / TM Owner

Laboratoires Chaix Et Du Marais

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Indications & Clinical Uses

Mannitol is used in clinical situations that require rapid osmotic diuresis or reduction of fluid pressure.

  • Intracranial hypertension: lowers intracranial pressure by drawing fluid from brain tissue into the vascular compartment.
  • Acute renal failure: promotes urine output to assist renal clearance when kidney function is compromised.
  • Ocular hypertension: reduces intraocular pressure during surgical procedures or acute attacks.
  • Fluid overload in cardiac surgery: facilitates removal of excess extracellular fluid to improve hemodynamic stability.
  • Hyperosmolar emergencies: provides rapid plasma osmolarity increase to manage severe hypernatremia.

How It Works

  • Mannitol acts as an osmotically active agent that raises plasma osmolality when administered intravenously. The increased extracellular osmotic pressure draws water from intracellular and interstitial compartments into the vascular space, expanding intravascular volume and promoting renal filtration. The resulting diuresis helps to lower intracranial and intraocular pressures and to flush renal tubules in acute kidney injury. It does not undergo significant metabolism and is eliminated unchanged by glomerular filtration.

Side Effects

Mannitol may be associated with a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Headache: mild to moderate pain often reported during infusion.
  • Nausea or vomiting: gastrointestinal discomfort occurring shortly after administration.
  • Electrolyte imbalance: shifts in sodium or potassium levels.
  • Thirst or dry mouth: sensation of increased fluid need.
  • Transient hypotension: mild drop in blood pressure during rapid infusion.
  • Dizziness: light‑headed feeling during or after infusion.

Serious or Rare Side Effects

  • Pulmonary edema: accumulation of fluid in lungs, especially in patients with cardiac dysfunction.
  • Acute renal failure worsening: paradoxical decrease in urine output.
  • Severe electrolyte disturbances: hypernatremia or hyponatremia requiring urgent correction.
  • Anaphylactic reaction: rare hypersensitivity with rash, bronchospasm, or circulatory collapse.
  • Seizures: rare neurologic event linked to rapid osmotic shifts.

Precautions & Warnings

When using Mannitol, clinicians should observe specific precautions to minimise risks and ensure therapeutic effectiveness.

  • Assess renal function: confirm adequate glomerular filtration before initiating therapy.
  • Monitor fluid balance: track input and output to avoid overload.
  • Check electrolytes: regularly measure serum sodium and potassium levels.
  • Adjust infusion rate: use controlled infusion to prevent rapid plasma osmolar changes.
  • Avoid in severe heart failure: risk of pulmonary edema is heightened.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Mannitol can interact with several medicines, influencing its efficacy or safety profile.

Major Interactions (Avoid)

  • Loop diuretics: may potentiate excessive diuresis and electrolyte loss.
  • Lithium: increased risk of lithium toxicity due to altered renal clearance.
  • Antihypertensives: additive hypotensive effect when combined with rapid infusion.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: monitor blood pressure and renal function.
  • Aminoglycoside antibiotics: watch for nephrotoxicity when renal perfusion is reduced.
  • Insulin: osmotic shifts may affect glucose control, requiring dose adjustment.

Frequently Asked Questions

Mannitol Lavoisier is an osmotic diuretic indicated for lowering elevated intracranial pressure, promoting diuresis in acute renal failure, and reducing intraocular pressure during ophthalmic procedures. It is administered intravenously in hospital or critical‑care settings to manage fluid shifts and support renal clearance.

Mannitol increases plasma osmolality when given intravenously, creating an osmotic gradient that pulls water from intracellular and interstitial spaces into the vascular compartment. This expands intravascular volume, enhances glomerular filtration, and facilitates the removal of excess fluid, thereby decreasing pressure in the brain and eyes.

The dose of Mannitol Lavoisier is individualized by the prescribing clinician based on the patient’s weight, renal function, severity of the condition, and target osmolar goals. No fixed regimen is provided here; the prescriber sets the appropriate infusion rate and total amount.

Mannitol’s pregnancy category is not definitively established, and limited data are available. Caution is advised when prescribing to pregnant or lactating women, and the potential benefits should be weighed against possible risks. Consultation with a specialist is recommended.

To order Mannitol Lavoisier, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Mannitol is the most widely used osmotic diuretic and is distinguished by its rapid onset, predictable plasma osmolar increase, and renal elimination unchanged. Compared with agents such as hypertonic saline, Mannitol provides a stronger osmotic gradient with fewer electrolyte disturbances when administered correctly.

Mannitol Lavoisier should be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. Keep the vial in its original packaging until use, and inspect for particulate matter or discoloration before administration.

Mannitol Lavoisier is given by intravenous infusion. The solution is typically diluted in compatible IV fluids and administered over a controlled period, often using an infusion pump to achieve the desired rate and avoid rapid osmotic shifts.

Serious risks include pulmonary edema, especially in patients with compromised cardiac function, worsening renal failure with reduced urine output, severe electrolyte disturbances such as hypernatremia, and rare anaphylactic reactions that require immediate medical intervention.

Mannitol is contraindicated in patients with established severe heart failure, active pulmonary edema, severe dehydration, or known hypersensitivity to mannitol. Caution is also advised in individuals with uncontrolled electrolyte imbalances or those at high risk for intracranial hemorrhage.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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