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

Mannitol Bradex

Active Ingredient:
Mannitol
Origin:
EU

Mannitol Bradex (Mannitol)

Mannitol, the active ingredient in Mannitol Bradex, is an osmotic diuretic presented as a sterile solution for injection for intravenous use. It is employed to lower elevated intracranial pressure, decrease intraocular pressure, and to induce diuresis in patients with renal impairment or acute kidney injury.

GNH India supplies Mannitol Bradex as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres and pharmacies worldwide, providing reliable access to this essential renal‑therapy agent with consistent quality control and regulatory compliance across EU and global markets.

Manufacturer / TM Owner

Bradex S.A.

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Indications & Clinical Uses

  • Mannitol is an osmotic agent used in conditions where reduction of fluid pressure is required.
  • Intracranial hypertension: lowers intracranial pressure to prevent cerebral edema.
  • Intraocular pressure elevation: reduces intraocular pressure in acute glaucoma attacks.
  • Renal failure with oliguria: promotes diuresis to manage fluid overload.
  • Peri‑operative kidney transplantation: supports urine output during surgical management.

How It Works

  • Mannitol acts as an osmotic diuretic by increasing extracellular osmolarity when administered intravenously. The elevated osmolarity draws water from intracellular and interstitial spaces into the vascular compartment, expanding plasma volume and enhancing renal filtration. This osmotic gradient promotes urine formation and reduces fluid pressure in the brain and eye, facilitating the therapeutic effects in the indicated conditions.

Side Effects

Mannitol may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Headache: transient headache occurring during or after infusion.
  • Nausea or vomiting: gastrointestinal upset related to osmotic load.
  • Electrolyte imbalance: especially hypokalemia or hyponatremia.
  • Dehydration or hypotension: due to rapid fluid shifts.

Serious or Rare Side Effects

  • Pulmonary edema: fluid accumulation in lungs, requiring immediate attention.
  • Severe electrolyte disturbances: hypernatremia or severe hypokalemia.
  • Anaphylactoid reaction: rare hypersensitivity with rash or bronchospasm.
  • Worsening renal failure: in patients with pre‑existing severe kidney dysfunction.

Precautions & Warnings

  • Mannitol requires careful monitoring and specific safety measures.
  • Renal function: monitor urine output and serum electrolytes closely.
  • Cardiovascular status: watch for hypotension, especially in hypovolemic patients.
  • Pregnancy: category C; use only if potential benefit justifies the risk.
  • Electrolyte balance: correct pre‑existing abnormalities before infusion.
  • Concurrent nephrotoxic drugs: avoid or monitor closely for additive renal risk.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Mannitol can interact with several drug classes, influencing safety and efficacy.

Major Interactions (Avoid)

  • Loop diuretics: may cause excessive fluid loss and electrolyte depletion.
  • Insulin: hyperosmolar state can impair glucose control, requiring dose adjustment.
  • ACE inhibitors: increased risk of profound hypotension.

Moderate Interactions (Monitor Closely)

  • Antihypertensive agents: may potentiate blood pressure reduction.
  • Nephrotoxic antibiotics (e.g., aminoglycosides): heightened risk of renal injury.

Frequently Asked Questions

Mannitol Bradex is a sterile intravenous solution of mannitol, an osmotic diuretic used to lower elevated intracranial pressure, reduce intraocular pressure in acute glaucoma, and promote diuresis in patients with renal failure or fluid overload.

Mannitol increases the osmolarity of the extracellular fluid after intravenous administration. This osmotic gradient pulls water from cells and interstitial spaces into the bloodstream, expanding plasma volume, enhancing renal filtration, and decreasing pressure in the brain and eye.

The dosage of Mannitol Bradex is determined by the prescribing clinician based on the specific indication, patient weight, renal function, and clinical response. The prescriber sets the infusion rate and total amount required for each individual case.

Mannitol is classified as pregnancy category C, meaning it should be used only if the potential benefit justifies the potential risk to the fetus. Limited data are available for breastfeeding; the decision should be made by a healthcare professional.

To order Mannitol Bradex, submit an enquiry on the product page at gnhindia.com indicating 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 if needed) and import documentation.

Mannitol is a widely used osmotic diuretic with a rapid onset of action and predictable pharmacokinetics. Compared with alternatives such as hypertonic saline, mannitol provides both diuretic and pressure‑reducing effects, but selection depends on the clinical scenario, patient tolerance, and physician preference.

Mannitol Bradex 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 and discard any solution that appears discolored or contains particles.

Mannitol Bradex is administered intravenously by a healthcare professional. The solution is typically diluted with compatible IV fluids and infused over a prescribed period, with monitoring of vital signs and urine output throughout the administration.

Serious risks include pulmonary edema, severe electrolyte disturbances such as hypernatremia or hypokalemia, anaphylactoid reactions, and worsening renal failure in susceptible patients. Prompt recognition and management of these events are essential.

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

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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