Product image of Manitol Viaflo Baxter Czech Spol (Mannitol) supplied by GNH India

Manitol Viaflo Baxter Czech Spol

Active Ingredient:
Mannitol
Origin:
EU

Manitol Viaflo Baxter Czech Spol (Mannitol)

Mannitol, the active ingredient in Manitol Viaflo Baxter Czech Spol, is an osmotic diuretic presented as an intravenous solution for IV use. It is employed to lower intracranial and intraocular pressure, promote diuresis in acute renal failure, and assist in glaucoma management.

GNH India supplies Manitol Viaflo Baxter Czech Spol as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide. The company adheres to stringent quality standards and provides reliable logistics for global healthcare institutions.

Manufacturer / TM Owner

Baxter Czech Spol. S R.O.

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Indications & Clinical Uses

Manitol is used in several clinical situations that require rapid osmotic fluid shifts.

  • Intracranial pressure elevation: Reduces cerebral edema and lowers intracranial pressure.
  • Acute renal failure: Enhances renal perfusion and promotes urine output.
  • Glaucoma: Lowers intraocular pressure during acute attacks.
  • Diuresis promotion: Facilitates fluid removal in patients needing controlled diuresis.

How It Works

  • Mannitol acts as an osmotic agent that does not readily cross intact cell membranes. After intravenous infusion it raises plasma osmolarity, pulling water from intracellular and interstitial spaces into the vascular compartment. The increased osmotic load is filtered by the kidneys, creating a tubular gradient that limits water reabsorption, producing diuresis, while the resulting fluid shift from the brain and eye reduces intracranial and intraocular pressure.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate intensity.
  • Nausea or vomiting: gastrointestinal upset.
  • Electrolyte imbalance: especially hyponatremia or hypernatremia.
  • Transient hypotension: due to rapid plasma volume expansion.
  • Fluid overload: in patients with compromised cardiac function.

Serious or Rare Side Effects

  • Acute renal failure: worsening kidney function.
  • Pulmonary edema: fluid accumulation in lungs.
  • Severe electrolyte disturbances: such as hyperkalemia.
  • Anaphylactoid reactions: rare hypersensitivity.
  • Hemolysis: in patients with G6PD deficiency.

Precautions & Warnings

When using mannitol, clinicians should observe specific precautions to minimize risks and ensure optimal therapy.

  • Renal function assessment: evaluate baseline creatinine and urine output before initiation.
  • Cardiovascular status: monitor for signs of fluid overload or heart failure.
  • Electrolyte monitoring: check serum sodium, potassium, and osmolality regularly.
  • Neurological monitoring: assess intracranial pressure trends and neurological status.
  • Pregnancy and lactation: use only if potential benefits justify potential risks, as safety data are limited.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Mannitol can interact with several medicines, altering its efficacy or increasing toxicity.

Major Interactions (Avoid)

  • Loop diuretics (e.g., furosemide): may cause excessive diuresis and electrolyte loss.
  • Nephrotoxic agents (e.g., aminoglycosides, amphotericin B): increased risk of renal impairment.

Moderate Interactions (Monitor Closely)

  • Antihypertensives: additive hypotensive effect.
  • Insulin or oral hypoglycemics: altered glucose control due to fluid shifts.
  • Lithium: risk of lithium toxicity from altered renal clearance.
  • Anticoagulants: potential for increased bleeding if renal function declines.

Frequently Asked Questions

Manitol Viaflo Baxter Czech Spol is an intravenous osmotic diuretic indicated for rapid reduction of elevated intracranial pressure, management of acute renal failure to promote urine output, and treatment of acute glaucoma attacks by lowering intraocular pressure. It is also employed when controlled diuresis is required in critical care settings.

Mannitol works by increasing the osmolarity of plasma and renal tubular fluid after intravenous administration. The heightened osmotic gradient draws water from intracellular and interstitial compartments into the vascular space, enhancing renal filtration and urine production while decreasing fluid volume in the brain and eye, thereby lowering intracranial and intraocular pressures.

The dose of mannitol is individualized and set by the prescribing clinician based on the specific indication, patient weight, renal function, and desired therapeutic effect. Dosage regimens are tailored to achieve target osmolarity and clinical response while monitoring for safety parameters.

Safety data for mannitol during pregnancy and lactation are limited. It should be used only when the potential benefits outweigh any possible 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 necessary import documentation.

Both mannitol and hypertonic saline create an osmotic gradient to reduce intracranial pressure, but mannitol is filtered by the kidneys and promotes diuresis, whereas hypertonic saline remains in the extracellular space and expands plasma volume. Choice depends on the patient’s renal function, volume status, and specific clinical goals.

Manitol intravenous solution should be stored at 2‑8 °C, protected from light, and must not be frozen or shaken. Keep the product in its original packaging until use and discard any solution that appears discolored or contains particles.

Mannitol is administered by slow intravenous infusion, typically through a dedicated line or infusion pump. The infusion rate and total volume are determined by the prescriber, and the solution should be administered under continuous clinical monitoring.

Serious risks include acute renal failure, pulmonary edema, severe electrolyte disturbances (especially hypernatremia or hyperkalemia), and rare anaphylactoid reactions. Prompt recognition of these events and immediate medical intervention are essential.

Mannitol is contraindicated in patients with known hypersensitivity to mannitol, severe renal impairment, active intracranial hemorrhage where increased osmolarity could worsen bleeding, and in individuals with uncontrolled heart failure or pulmonary edema where fluid shifts may be harmful.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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