Product image of Mannitol, Viaflo Baxter (Mannitol) supplied by GNH India

Mannitol, Viaflo Baxter

Active Ingredient:
Mannitol
Origin:
EU

Mannitol, Viaflo Baxter (Mannitol)

Mannitol, the active ingredient in Viaflo Baxter, is an osmotic diuretic presented as a solution for injection for intravenous use. It reduces intracranial pressure, promotes diuresis in acute renal failure, and lowers intraocular pressure in glaucoma patients.

GNH India supplies Viaflo Baxter as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Baxter Medical Ab

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Indications & Clinical Uses

Mannitol is employed as an osmotic diuretic in several clinical situations that require rapid fluid shift.

  • Intracranial hypertension: reduces intracranial pressure by drawing water from brain tissue into the vascular compartment.
  • Acute renal failure: promotes diuresis to facilitate renal clearance of waste products.
  • Glaucoma: lowers intraocular pressure by osmotic dehydration of the vitreous humor.
  • Intraocular pressure elevation: decreases pressure within the eye, aiding in the management of ocular hypertension.

How It Works

  • Intravenous Mannitol increases plasma osmolality, creating an osmotic gradient that pulls water from intracellular and tissue compartments into the extracellular space. The resulting plasma expansion enhances glomerular filtration, promotes renal excretion of water and electrolytes, and reduces pressure in confined compartments such as the cranial vault and the eye, thereby achieving its therapeutic effects.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate intensity.
  • Nausea and vomiting: gastrointestinal upset following infusion.
  • Thirst or dry mouth: due to osmotic effect.
  • Electrolyte disturbances: mild hyponatremia or hypernatremia.
  • Transient hypotension: drop in blood pressure during rapid infusion.
  • Tachycardia: increased heart rate secondary to volume shifts.

Serious or Rare Side Effects

  • Pulmonary edema: fluid accumulation in lungs.
  • Severe electrolyte imbalance: marked hypernatremia or hypokalemia.
  • Acute renal failure worsening: reduced kidney function.
  • Anaphylactic reaction: rare hypersensitivity.
  • Hemolysis: destruction of red blood cells.
  • Hyperosmolar coma: extreme plasma osmolality.

Precautions & Warnings

When using Mannitol, clinicians should observe several precautionary measures to minimize risk.

  • Renal function: assess baseline renal performance and avoid use in anuric patients.
  • Electrolytes: monitor serum sodium, potassium and osmolality before and during therapy.
  • Cardiac status: use cautiously in patients with heart failure or volume overload.
  • Fluid balance: avoid excessive infusion rates that may cause circulatory overload.
  • Pregnancy: consider only if potential benefit justifies potential risk, as safety data are limited.
  • Store at ambient temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Mannitol can interact with other medicines, influencing their efficacy or safety.

Major Interactions (Avoid)

  • Loop diuretics: additive diuretic effect may cause profound electrolyte loss.
  • Insulin: hyperosmolar state can impair glucose control.
  • Nephrotoxic agents: increased risk of renal injury when combined.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: monitor blood pressure and renal function for additive effects.
  • Antihypertensive drugs: potential for enhanced hypotension.
  • Lithium: altered renal clearance may raise lithium levels.

Frequently Asked Questions

Mannitol (Viaflo Baxter) is an osmotic diuretic indicated for the reduction of elevated intracranial pressure, promotion of diuresis in acute renal failure, and lowering of intraocular pressure in glaucoma or other ocular hypertension conditions.

Mannitol works by increasing plasma osmolality after intravenous administration, creating an osmotic gradient that draws water from intracellular and tissue spaces into the vascular compartment, thereby expanding plasma volume, enhancing renal filtration, and reducing pressure in confined compartments such as the brain and eye.

The dose of Mannitol is individualized by the prescribing clinician based on the specific indication, patient weight, renal function, and desired therapeutic effect. Dosage regimens are not standardized and must be set by a qualified health professional.

Mannitol is classified as pregnancy category unknown. It should only be used during pregnancy or lactation when the potential benefit justifies any possible risk to the fetus or infant, and the decision should be made by the treating physician.

To order Viaflo Baxter, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if required) and import documentation.

Mannitol is a sugar‑alcohol osmotic agent that rapidly raises plasma osmolality, whereas alternatives such as hypertonic saline achieve similar effects with different electrolyte profiles. Mannitol’s renal clearance and predictable osmotic effect make it a preferred choice for acute intracranial pressure and renal diuresis, but individual patient factors guide selection.

Mannitol solution for injection should be stored at ambient temperature, kept in its original packaging, protected from light and moisture, and inspected for particulate matter before use. Do not freeze or shake the vial.

Mannitol is administered intravenously, typically diluted in compatible IV fluids and infused over a controlled period as directed by the prescriber. The infusion rate is adjusted according to the clinical response and monitored parameters such as blood pressure and serum osmolality.

Serious risks include pulmonary edema, severe electrolyte disturbances (especially hypernatremia), worsening renal failure, anaphylactic reactions, hemolysis, and hyperosmolar coma. Patients should be closely monitored for these events, particularly during high‑dose or rapid infusions.

Mannitol is contraindicated in patients with anuria, severe renal impairment, active intracranial hemorrhage, uncontrolled electrolyte imbalances, severe heart failure, or known hypersensitivity to mannitol. Use in these populations may exacerbate underlying conditions and lead to serious complications.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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