Product image of Mannitol Bieffe (Mannitol) supplied by GNH India

Mannitol Bieffe

Active Ingredient:
Mannitol
Origin:
EU

Mannitol Bieffe (Mannitol)

Mannitol, the active ingredient in Mannitol Bieffe, is an osmotic diuretic presented as a sterile solution for injection for intravenous use. It increases plasma osmolality, drawing water from tissues into the vascular compartment, thereby reducing intracranial and intraocular pressure and supporting renal diuresis in acute renal failure.

GNH India supplies Mannitol Bieffe as a licensed, GDP‑compliant product sourced from the European Union, providing hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide with a reliable source of this essential osmotic agent.

Manufacturer / TM Owner

Baxter Slovakia S.R.O.

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Indications & Clinical Uses

Mannitol is used as an osmotic agent to manage conditions associated with elevated intracranial or intraocular pressure and to promote diuresis.

  • Intracranial hypertension: lowers intracranial pressure by drawing fluid from brain tissue into the bloodstream.
  • Glaucoma: reduces intraocular pressure, helping to prevent optic nerve damage.
  • Acute renal failure: enhances renal excretion of water and electrolytes, supporting urine output.

How It Works

  • Mannitol acts as an osmotic diuretic by increasing plasma osmolality when administered intravenously. The elevated osmolality creates an osmotic gradient that pulls water from intracellular and interstitial spaces into the vascular compartment, expanding plasma volume and promoting renal filtration. This shift reduces pressure in confined compartments such as the cranial and ocular spaces and stimulates diuresis.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate headache reported during infusion.
  • Nausea or vomiting: gastrointestinal discomfort occurring shortly after administration.
  • Electrolyte imbalance: transient changes in sodium or potassium levels.
  • Fluid overload: signs of volume expansion such as peripheral edema.
  • Transient hypotension: brief drop in blood pressure during rapid infusion.

Serious or Rare Side Effects

  • Acute renal failure: worsening kidney function in susceptible patients.
  • Pulmonary edema: accumulation of fluid in the lungs, especially with excessive dosing.
  • Severe electrolyte disturbances: hypernatremia or hypokalemia requiring intervention.
  • Anaphylactoid reaction: rare hypersensitivity with rash, bronchospasm, or shock.

Precautions & Warnings

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

  • Assess renal function: evaluate creatinine clearance before initiation.
  • Monitor fluid balance: track input/output and weight to avoid overload.
  • Check electrolytes: regularly measure serum sodium, potassium, and osmolality.
  • Use controlled infusion rate: administer slowly to reduce hypotension and pain.
  • Avoid in patients with severe pulmonary congestion: risk of worsening edema.
  • 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 safety profile.

Major Interactions (Avoid)

  • Loop diuretics: concurrent use may exacerbate electrolyte loss and dehydration.
  • Lithium: increased risk of lithium toxicity due to altered renal clearance.

Moderate Interactions (Monitor Closely)

  • Antihypertensives: additive hypotensive effect, monitor blood pressure.
  • Aminoglycoside antibiotics: potential for enhanced nephrotoxicity.
  • Insulin or oral hypoglycemics: osmotic shifts may affect glucose control.
  • Contrast media: combined osmotic load can increase risk of renal impairment.

Frequently Asked Questions

Mannitol Bieffe is an intravenous osmotic diuretic employed to lower elevated intracranial pressure, reduce intraocular pressure in glaucoma, and promote diuresis in patients with acute renal failure. By drawing fluid from tissues into the bloodstream, it helps manage these critical conditions under medical supervision.

Mannitol increases plasma osmolality when infused intravenously, creating an osmotic gradient that pulls water from intracellular and interstitial compartments into the vascular space. This fluid shift expands plasma volume, lowers pressure in confined areas such as the brain and eye, and stimulates renal filtration, resulting in diuresis.

The dose of Mannitol Bieffe is individualized by the prescribing clinician based on the specific indication, patient weight, renal function, and desired therapeutic effect. Dosage regimens are adjusted according to clinical response and laboratory monitoring, and no fixed dosing schedule is provided in product literature.

Safety data for Mannitol in pregnancy and lactation are limited, and the product is classified as having an unknown pregnancy category. It should only be used when the potential benefits to the mother outweigh any possible risks to the fetus or infant, and under close medical supervision.

To order Mannitol Bieffe, 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 necessary import documentation.

Mannitol is a widely used osmotic diuretic that provides rapid plasma osmolality increase, whereas alternatives such as hypertonic saline may have a slower onset and different electrolyte effects. Mannitol’s renal clearance and predictable osmotic action make it preferred for acute pressure reduction, though choice depends on patient-specific factors and clinician judgment.

Mannitol Bieffe should be stored at 2‑8 °C in a refrigerator, protected from light. The solution must not be frozen or shaken, and it should remain in its original packaging until use to maintain sterility and potency.

Mannitol Bieffe is administered by intravenous infusion. It is typically diluted in an appropriate compatible IV fluid and infused at a controlled rate, as directed by the prescriber, to avoid rapid plasma osmolality changes that could cause hypotension or discomfort.

The most serious risks include acute renal failure, pulmonary edema, severe electrolyte disturbances such as hypernatremia or hypokalemia, and rare anaphylactoid reactions. Patients should be closely monitored for changes in renal function, fluid status, and vital signs throughout therapy.

Mannitol Bieffe is contraindicated in patients with anuria, severe pulmonary congestion or edema, known hypersensitivity to mannitol, and in those where rapid fluid shifts could be hazardous. Clinicians must evaluate each patient’s medical history before initiating therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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