Product image of Mannit Fresenius (Mannitol) supplied by GNH India

Mannit Fresenius

Active Ingredient:
Mannitol
Origin:
EU

Mannit Fresenius (Mannitol)

Mannitol, the active ingredient in Mannit Fresenius, is an osmotic diuretic presented as a sterile injection solution for intravenous use. It works by increasing plasma osmolality, drawing fluid from intracellular and interstitial spaces into the vascular compartment, which helps lower intracranial and intraocular pressure and supports diuresis in patients with acute renal failure.

GNH India supplies Mannit Fresenius as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres and pharmacies worldwide, ensuring quality and regulatory compliance.

Manufacturer / TM Owner

Fresenius Kabi Austria Gmbh

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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 in renal impairment.

  • Intracranial hypertension: lowers intracranial pressure and helps prevent cerebral edema.
  • Intraocular hypertension: reduces intraocular pressure in acute glaucoma or ocular surgery.
  • Acute renal failure: promotes diuresis to facilitate fluid removal and improve renal perfusion.

How It Works

  • Mannitol increases plasma osmolality by remaining largely extracellular after intravenous infusion. The resulting osmotic gradient draws water from intracellular and interstitial compartments into the vascular space, expanding plasma volume, reducing cerebral and ocular edema, and enhancing renal tubular flow to produce a diuretic effect.

Side Effects

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

Common Side Effects

  • Headache
  • Nausea or vomiting
  • Transient hypotension
  • Electrolyte disturbances (e.g., hyponatremia, hypokalemia)
  • Flushing or feeling of warmth

Serious or Rare Side Effects

  • Pulmonary edema
  • Acute renal failure or worsening kidney function
  • Severe hypernatremia
  • Hemolysis in patients with G6PD deficiency
  • Anaphylactic or severe allergic reactions

Precautions & Warnings

Mannitol administration requires careful assessment of patient condition and monitoring of fluid and electrolyte balance.

  • Renal function: avoid or adjust use in patients with pre‑existing renal impairment.
  • Cardiovascular status: monitor for volume overload and hypotension, especially in heart failure.
  • Electrolytes: check serum sodium and potassium before and during therapy.
  • Pregnancy and lactation: use only if clearly needed; safety data are limited.
  • Concomitant diuretics: assess risk of excessive fluid loss.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake the vial.

Avoid Interactions

Mannitol can interact with several medications, altering its efficacy or increasing risk of adverse events.

Major Interactions (Avoid)

  • Loop diuretics (e.g., furosemide): may exacerbate electrolyte loss and renal dysfunction.
  • Nephrotoxic agents (e.g., aminoglycosides, amphotericin B): increase risk of kidney injury.

Moderate Interactions (Monitor Closely)

  • Insulin: rapid shifts in plasma osmolality can affect glucose control.
  • Lithium: altered renal clearance may raise lithium levels.
  • Antihypertensives: additive hypotensive effect may require dose adjustment.

Frequently Asked Questions

Mannit Fresenius contains mannitol, an osmotic diuretic administered intravenously to lower intracranial and intraocular pressure and to promote diuresis in patients with acute renal failure.

Mannitol remains largely in the extracellular space after IV infusion, raising plasma osmolality. This osmotic gradient pulls water from cells and interstitial tissue into the bloodstream, reducing edema in the brain and eye and increasing urine output by enhancing renal tubular flow.

The dose of Mannit Fresenius is determined by the prescribing clinician based on the specific indication, patient weight, renal function, and clinical response. No fixed regimen is provided here.

Safety data for mannitol in pregnancy and lactation are limited. It should be used only if the potential benefit justifies any potential risk to the fetus or infant, and the decision must be made by the treating physician.

To place an 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 plasma‑osmotic effects. Compared with hypertonic saline, mannitol provides both volume expansion and diuresis, making it preferred for acute reduction of intracranial pressure and for renal protection in certain settings.

Mannit Fresenius should be stored at 2‑8 °C, protected from light, and must not be frozen or shaken. Keep the vial in its original packaging until use to maintain sterility and potency.

Mannit Fresenius is given as an intravenous injection or infusion. The rate and volume are set by the healthcare professional, who monitors the patient’s vital signs, fluid balance and serum electrolytes throughout the administration.

Serious risks include pulmonary edema, severe hypernatremia, acute renal failure, and anaphylactic reactions. Prompt recognition of these events and immediate medical intervention are essential to mitigate harm.

Mannit Fresenius is contraindicated in patients with known hypersensitivity to mannitol, severe renal impairment where diuresis is ineffective, active pulmonary edema, and in those with severe electrolyte disturbances that could be worsened by osmotic shifts.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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