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

Mannitol Βιοσερ

Active Ingredient:
Mannitol
Origin:
EU

Mannitol Βιοσερ (Mannitol)

Mannitol, the active ingredient in Mannitol Βιοσερ, is an osmotic diuretic presented as a solution for injection for intravenous use. It reduces intracranial pressure and promotes diuresis in patients with renal failure or ocular hypertension.

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

Manufacturer / TM Owner

Vioser S.A.

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Indications & Clinical Uses

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

  • Reduction of intracranial pressure: lowers cerebral edema and intracranial pressure in traumatic brain injury or neurosurgical patients.
  • Oliguric renal failure: increases urine output to manage acute kidney injury with low urine output.
  • Intraocular pressure elevation: facilitates aqueous humor outflow to lower intraocular pressure during ocular surgery.

How It Works

  • Mannitol acts as an osmotically active agent that raises plasma osmolality when administered intravenously. The increased extracellular osmotic pressure draws water from intracellular and interstitial compartments into the vascular space, expanding plasma volume and promoting renal filtration. This osmotic gradient also reduces cerebral and intraocular fluid accumulation, thereby decreasing intracranial and intraocular pressures.

Side Effects

Mannitol may cause a range of adverse reactions, from mild to severe, depending on patient factors and dosage.

Common Side Effects

  • Headache: mild to moderate pain often reported during infusion.
  • Nausea and vomiting: gastrointestinal upset occurring shortly after administration.
  • Dizziness or light‑headedness: related to rapid plasma volume shifts.
  • Thirst or dry mouth: due to osmotic water movement.
  • Electrolyte imbalance: mild changes in sodium or potassium levels.

Serious or Rare Side Effects

  • Pulmonary edema: fluid accumulation in the lungs, especially in patients with cardiac dysfunction.
  • Severe electrolyte disturbances: hypernatremia, hyperkalemia, or profound hyponatremia.
  • Worsening renal failure: especially in patients with pre‑existing kidney impairment.
  • Anaphylactic or severe allergic reaction: rare but requires immediate medical attention.
  • Hemolysis: rare destruction of red blood cells.
  • Cardiac arrhythmia: associated with electrolyte shifts.

Precautions & Warnings

Before initiating Mannitol therapy, clinicians should evaluate patient-specific risk factors and monitor relevant parameters.

  • Assess renal function: evaluate baseline creatinine and urine output before administration.
  • Monitor electrolytes: check serum sodium, potassium, and osmolality during therapy.
  • Avoid in severe dehydration: ensure adequate volume status to prevent hypotension.
  • Use cautiously in heart failure: risk of fluid overload and pulmonary edema.
  • 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 avoid additive or harmful effects.

Major Interactions (Avoid)

  • Loop diuretics: additive diuretic effect may cause severe electrolyte loss.
  • Insulin: hyperosmolarity may potentiate hypoglycemia.
  • Lithium: increased risk of lithium toxicity due to altered renal clearance.
  • ACE inhibitors/ARBs: may exacerbate renal impairment when combined.

Moderate Interactions (Monitor Closely)

  • Antihypertensives: may enhance blood pressure lowering.
  • Nephrotoxic antibiotics (e.g., aminoglycosides): monitor renal function closely.
  • Contrast media: increased risk of renal dysfunction when used together.

Frequently Asked Questions

Mannitol Βιοσερ is an intravenous osmotic diuretic indicated for rapid reduction of elevated intracranial pressure, promotion of diuresis in oliguric renal failure, and lowering intraocular pressure during ocular procedures. It is employed in acute care settings where swift fluid shifts are required.

Mannitol increases plasma osmolality after intravenous infusion, creating an osmotic gradient that pulls water from intracellular and interstitial spaces into the vascular compartment. This expands plasma volume, enhances renal filtration, and reduces fluid accumulation in the brain and eye, thereby lowering pressure.

The specific dose of Mannitol is determined by the prescribing clinician based on the patient’s condition, weight, renal function, and therapeutic goal. Dosing regimens are individualized and should follow the prescriber’s order and institutional protocols.

Mannitol’s pregnancy category is listed as unknown. It should only be used during pregnancy or lactation when the potential benefit justifies any possible risk to the fetus or infant, and after careful evaluation by the treating physician.

To order Mannitol Βιοσερ, 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 non‑metabolizable sugar alcohol that exerts a rapid osmotic effect, whereas other agents like hypertonic saline rely on sodium load to increase osmolality. Mannitol’s high osmotic coefficient makes it especially effective for acute reduction of intracranial and intraocular pressure, but it requires careful monitoring of renal function and electrolytes.

Mannitol Βιοσερ should be stored at 2‑8 °C in a refrigerator, protected from light. Do not freeze the solution or shake the vial vigorously. Keep the product in its original packaging until use to maintain sterility and stability.

Mannitol is administered intravenously as a sterile solution for injection. It is typically given as a bolus or continuous infusion, depending on the clinical indication and physician’s order. Administration must be performed by qualified healthcare personnel using aseptic technique.

Serious risks include pulmonary edema, severe electrolyte disturbances (such as hypernatremia or hyperkalemia), worsening renal failure, and rare anaphylactic reactions. Prompt recognition of respiratory distress, abrupt changes in serum electrolytes, or signs of allergic response is essential for patient safety.

Mannitol is contraindicated in patients with severe dehydration, active intracranial hemorrhage where increased volume could worsen bleeding, uncontrolled heart failure, and known hypersensitivity to mannitol or any component of the formulation. Clinicians should also avoid use in patients with established anuria unless under strict monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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