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

GNH India supplies Mannitol, Viaflo Baxter as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, transplant centres and pharmacies worldwide.

Manufacturer / TM Owner

Baxter Sa

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Indications & Clinical Uses

Mannitol is an osmotic diuretic used in conditions where reduction of fluid pressure is required.

  • Intracranial pressure: lowers pressure to protect brain tissue.
  • Cerebral edema: decreases brain swelling and improves neurological outcomes.
  • Acute renal failure: promotes diuresis to aid renal clearance.
  • Intraocular pressure: reduces pressure to help manage glaucoma and ocular emergencies.

How It Works

  • Mannitol increases the osmotic pressure of the extracellular fluid and renal tubular lumen. By creating an osmotic gradient, it draws water from intracellular and interstitial spaces into the vascular compartment, enhancing urinary output and lowering intracranial and intraocular pressures without directly acting on receptors.

Side Effects

Mannitol may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Headache: mild to moderate discomfort.
  • Nausea or vomiting: gastrointestinal upset.
  • Electrolyte imbalance: especially hyponatremia or hyperkalemia.
  • Hypotension: transient drop in blood pressure.
  • Tachycardia: increased heart rate.

Serious or Rare Side Effects

  • Pulmonary edema: fluid accumulation in lungs.
  • Severe dehydration: excessive fluid loss.
  • Anaphylactic reaction: rare hypersensitivity.
  • Acute renal failure worsening: in patients with pre‑existing kidney impairment.
  • Cardiac arrhythmias: due to electrolyte disturbances.

Precautions & Warnings

When using Mannitol, clinicians should observe several safety measures.

  • Renal function monitoring: assess creatinine and urine output.
  • Electrolyte surveillance: check serum sodium, potassium, and osmolality.
  • Fluid balance assessment: avoid over‑ or under‑hydration.
  • Cardiovascular status: use cautiously in heart failure or hypotension.
  • Intracranial lesions: evaluate risk of rapid pressure shifts.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Mannitol can interact with other medicines, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Loop diuretics: may cause excessive diuresis and electrolyte loss.
  • Insulin: can alter glucose control when fluid shifts occur.
  • Lithium: increased risk of lithium toxicity.
  • ACE inhibitors: heightened hypotensive effect.

Moderate Interactions (Monitor Closely)

  • Antihypertensives: additive blood pressure lowering.
  • NSAIDs: may impair renal clearance.
  • Corticosteroids: can exacerbate fluid retention.
  • Anticonvulsants: monitor for altered serum levels.

Frequently Asked Questions

Mannitol, Viaflo Baxter is used as an osmotic diuretic to lower intracranial and intraocular pressure, treat cerebral edema, and promote urine output in patients with acute renal failure. It is administered intravenously in hospital or clinical settings.

Mannitol works by increasing the osmotic pressure of blood and renal tubular fluid. This draws water from cells and interstitial spaces into the vascular compartment, enhancing urinary excretion and reducing fluid pressure in the brain and eyes.

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

Mannitol’s pregnancy category is unknown, and safety data are limited. It should only be used during pregnancy or lactation when the potential benefit outweighs any possible risk to the fetus or infant, and under close medical supervision.

To order, 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 (including cold‑chain if needed) and import documentation.

Mannitol is a non‑ionic sugar alcohol that creates an osmotic gradient without crossing the blood‑brain barrier, unlike hypertonic saline which adds sodium. Mannitol’s rapid renal clearance makes it suitable for acute pressure reduction, while hypertonic saline may be preferred for sustained volume expansion.

Mannitol solution for injection should be stored at 2‑8 °C, protected from light, and never frozen or shaken. Keep the vial in its original packaging until use and discard any solution that appears discolored or contains particles.

Mannitol is given by intravenous infusion. The solution is typically diluted in compatible IV fluids and infused over a controlled period, as directed by the prescriber, to achieve the desired osmotic effect while monitoring patient response.

Serious risks include pulmonary edema, severe dehydration, electrolyte disturbances that can lead to cardiac arrhythmias, and rare anaphylactic reactions. Prompt recognition of these events and immediate medical intervention are essential.

Mannitol is contraindicated in patients with severe dehydration, anuria, active intracranial hemorrhage, uncontrolled heart failure, or known hypersensitivity to mannitol. Clinicians should assess each patient’s condition before initiating therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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