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 an osmotic diuretic presented as an intravenous solution for intravenous use. It is employed to lower elevated intracranial pressure and to protect renal function during acute kidney injury, particularly in critical care settings in adult patients.

GNH India supplies Mannitol Viaflo Baxter as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide, with a focus on quality assurance, regulatory compliance and reliable cold‑chain logistics for injectable products.

Manufacturer / TM Owner

Baxter Oy

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Indications & Clinical Uses

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

  • Intracranial hypertension: lowers elevated intracranial pressure by drawing fluid from brain tissue.
  • Acute kidney injury: provides renal protection by promoting osmotic diuresis and improving renal perfusion.
  • Oliguric states: induces diuresis to increase urine output in patients with low urine production.

How It Works

  • Mannitol increases extracellular osmolarity after intravenous administration, creating an osmotic gradient that draws water from intracellular and interstitial compartments into the vascular space. This shift promotes renal excretion of water and electrolytes, producing diuresis, and reduces cerebral edema by decreasing intracranial fluid volume.

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.
  • Thirst or dry mouth: due to osmotic effect.
  • Electrolyte imbalance: especially hyponatremia or hypokalemia.
  • Transient tachycardia: increased heart rate.
  • Mild hypotension: due to rapid fluid shifts.

Serious or Rare Side Effects

  • Pulmonary edema: fluid accumulation in lungs.
  • Severe electrolyte disturbances: hypernatremia, hyperkalemia.
  • Anaphylactoid reaction: rash, bronchospasm, hypotension.
  • Acute renal failure: worsening kidney function.
  • Cardiac arrhythmia: irregular heart rhythm.
  • Hemolysis: destruction of red blood cells.

Precautions & Warnings

Mannitol administration requires careful monitoring and specific safety measures.

  • Renal function: monitor serum electrolytes and renal parameters during therapy.
  • Intracranial pressure: use cautiously in patients with compromised cerebral perfusion.
  • Cardiovascular status: avoid rapid infusion in patients with heart failure.
  • Pregnancy: use only if potential benefits outweigh potential risks.
  • Allergy: discontinue immediately if hypersensitivity signs appear.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Mannitol can interact with several drug classes, requiring attention to dosing and monitoring.

Major Interactions (Avoid)

  • Loop diuretics: may cause excessive fluid loss and electrolyte imbalance.
  • Insulin: osmotic diuresis can alter glucose control, requiring dose adjustment.
  • Nephrotoxic agents: increased risk of renal impairment.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors: additive effect on renal function, monitor creatinine.
  • NSAIDs: may blunt diuretic response.
  • Antihypertensives: may enhance hypotensive effect.

Frequently Asked Questions

Mannitol Viaflo Baxter is an intravenous osmotic diuretic indicated for lowering elevated intracranial pressure, providing renal protection in acute kidney injury, and inducing diuresis in patients with reduced urine output. It is commonly used in intensive care, neurosurgery, and nephrology settings.

Mannitol works by increasing the osmolarity of the extracellular fluid after intravenous infusion. This creates an osmotic gradient that pulls water from cells and interstitial spaces into the bloodstream, promoting urinary excretion and reducing fluid accumulation in the brain, thereby decreasing intracranial pressure.

The dose of Mannitol is individualized by the prescribing clinician based on the patient’s weight, the specific indication, renal function, and desired therapeutic effect. Dosage regimens are established in clinical guidelines and adjusted according to response and laboratory monitoring.

Mannitol’s safety profile in pregnancy and lactation is not well established. It should be used only when the potential benefits justify the potential risks to the fetus or infant, and the decision should be made by the treating physician in consultation with the patient.

To order, submit an enquiry on the product page at gnhindia.com specifying 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 where required) and import documentation.

Mannitol is a widely used osmotic diuretic with rapid onset when given intravenously. Compared with hypertonic saline, Mannitol provides both diuretic and intracranial pressure‑lowering effects, but may cause more pronounced electrolyte shifts. Choice of agent depends on the clinical scenario, patient tolerance and physician preference.

Mannitol intravenous solution should be stored at 2‑8 °C, protected from light, and kept in its original container. Do not freeze or shake the solution. Before use, inspect for particulate matter or discoloration and allow the product to reach room temperature if required for infusion.

Mannitol is administered by intravenous infusion. It is typically diluted in a compatible IV fluid and infused over a controlled period, often 30‑60 minutes, depending on the indication and patient condition. Administration rate and concentration are determined by the prescriber and nursing protocols.

Serious risks include pulmonary edema, severe electrolyte disturbances (such as hyper

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GNH India Pharmaceuticals Limited

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