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 a solution for injection for intravenous use. It reduces intracranial pressure, promotes diuresis in acute renal failure, and is employed in clinical settings that require rapid fluid removal.

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

Manufacturer / TM Owner

Baxter Medical Ab

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Indications & Clinical Uses

Mannitol is used as an osmotic diuretic in several acute clinical conditions.

  • Intracranial hypertension: lowers intracranial pressure by drawing fluid from the brain into the vascular space.
  • Acute renal failure: enhances urine output to support renal clearance when kidney function is compromised.
  • Oliguric states: promotes diuresis in patients with low urine production to prevent fluid overload.
  • Glaucoma surgery: reduces intra‑ocular pressure during ophthalmic procedures.

How It Works

  • Mannitol acts as an osmotically active agent that remains largely extracellular after intravenous administration. By increasing plasma and tubular osmolarity, it creates an osmotic gradient that pulls water from intracellular and interstitial compartments into the vascular space, reducing cerebral edema and increasing urinary water excretion while limiting renal tubular reabsorption.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate discomfort often reported during infusion.
  • Nausea or vomiting: gastrointestinal upset occurring shortly after administration.
  • Thirst or dry mouth: sensation of increased dryness.
  • Transient hypotension: temporary drop in blood pressure during rapid infusion.

Serious or Rare Side Effects

  • Acute renal failure: worsening kidney function in susceptible patients.
  • Pulmonary edema: fluid accumulation in the lungs due to rapid volume shifts.
  • Severe electrolyte disturbances: hypernatremia or hypokalemia requiring intervention.
  • Anaphylactic reaction: rare hypersensitivity requiring emergency treatment.

Precautions & Warnings

Before using Mannitol, clinicians should consider several safety measures.

  • Assess renal function: evaluate baseline creatinine and urine output before initiating therapy.
  • Monitor fluid balance: record input and output closely to avoid volume overload.
  • Check electrolytes: regularly measure serum sodium, potassium, and osmolality during treatment.
  • Adjust infusion rate: infuse slowly to reduce risk of hypotension and cardiac stress.
  • Avoid in patients with severe dehydration: risk of exacerbating hypovolemia.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Mannitol can interact with other medicines, requiring careful management.

Major Interactions (Avoid)

  • Loop diuretics (e.g., furosemide): may cause excessive diuresis and electrolyte loss.
  • Nephrotoxic agents (e.g., aminoglycosides, amphotericin B): increase risk of renal impairment.
  • Insulin or oral hypoglycemics: osmotic shifts can potentiate hypoglycemia.
  • Hypertonic solutions: concurrent use can lead to severe hyperosmolar states.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: may enhance renal effects and affect blood pressure.
  • Antihypertensives: additive hypotensive effect during rapid infusion.
  • Lithium: altered renal clearance may increase lithium levels.

Frequently Asked Questions

Mannitol Viaflo Baxter is an intravenous osmotic diuretic used to lower elevated intracranial pressure, promote urine output in acute renal failure, and assist in managing oliguria or fluid overload in critical care settings.

Mannitol increases the osmolarity of plasma and renal tubular fluid, creating an osmotic gradient that draws water from cells and interstitial spaces into the bloodstream, thereby reducing cerebral edema and enhancing urinary water excretion.

The dose of Mannitol Viaflo Baxter is determined by the prescribing clinician based on the patient’s condition, weight, renal function, and therapeutic goals. Dosage regimens are individualized and should follow the prescriber’s order.

The safety of Mannitol in pregnancy and lactation has not been definitively established. It should be used only if the potential benefit justifies any potential risk to the fetus or infant, and under close medical supervision.

To order, submit an enquiry on the product page at gnhindia.com with 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 widely used osmotic diuretic with rapid onset and predictable renal excretion. Compared with hypertonic saline, it provides both volume expansion and diuresis, while agents like glycerol lack the same renal clearance profile, making Mannitol the preferred choice for acute intracranial pressure control.

Mannitol Viaflo Baxter should be stored at 2‑8 °C, protected from light, and kept in its original container. Do not freeze or shake the solution. Allow the product to reach room temperature before administration if required by the clinical protocol.

Mannitol Viaflo Baxter is administered intravenously, typically as an infusion over a prescribed period. The infusion rate and total volume are set by the healthcare professional to achieve the desired osmotic effect while monitoring patient tolerance.

Serious risks include acute renal failure, pulmonary edema, severe electrolyte disturbances (such as hypernatremia), and rare anaphylactic reactions. Continuous monitoring of renal function, fluid balance, and vital signs is essential to detect these complications early.

Mannitol is contraindicated in patients with severe dehydration, active intracranial bleeding, uncontrolled heart failure, or known hypersensitivity to mannitol. Caution is also advised for individuals with pre‑existing renal impairment or electrolyte abnormalities.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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