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

Mannitol Braun

Active Ingredient:
Mannitol
Origin:
EU

Mannitol Braun (Mannitol)

Mannitol, the active ingredient in Mannitol Braun, is an osmotic diuretic presented as a solution for injection for intravenous use. It is employed to increase plasma osmolality, drawing water from tissues into the vascular space, which helps reduce intracranial pressure and promotes diuresis in renal therapy. Mannitol Braun is manufactured in the European Union and conforms to EU pharmaceutical standards.

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

Manufacturer / TM Owner

B.Braun Melsungen Ag

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Indications & Clinical Uses

Mannitol is an osmotic diuretic used in several clinical situations that require rapid reduction of fluid volume in specific compartments.

  • Cerebral edema: lowers intracranial pressure by osmotic dehydration of brain tissue.
  • Acute renal failure with oliguria: promotes diuresis to facilitate renal clearance.
  • Elevated intraocular pressure: reduces pressure during ocular surgery or acute glaucoma.
  • Drug‑induced toxicity: enhances renal excretion of nephrotoxic agents such as contrast media.

How It Works

  • Mannitol acts as an osmotically active agent that does not readily cross cell membranes. When administered intravenously, it raises plasma osmolality, creating an osmotic gradient that pulls water from intracellular and interstitial spaces into the vascular compartment. This shift increases renal tubular flow, promotes diuresis, and reduces pressure in confined spaces such as the cranial and ocular compartments.

Side Effects

Mannitol injection may be associated with several adverse reactions, ranging from mild to severe.

Common Side Effects

  • Headache: transient discomfort due to fluid shifts.
  • Nausea or vomiting: gastrointestinal upset following infusion.
  • Thirst or dry mouth: result of increased plasma osmolality.
  • Electrolyte imbalance: especially hyponatremia or hypokalemia.
  • Transient hypotension: due to rapid intravascular volume expansion.

Serious or Rare Side Effects

  • Pulmonary edema: fluid overload in susceptible patients.
  • Acute renal failure: paradoxical worsening of kidney function.
  • Severe hyponatremia or hypernatremia: dangerous electrolyte disturbances.
  • Anaphylactic reaction: rare hypersensitivity to the solution.
  • Cardiac arrhythmia: secondary to electrolyte shifts.
  • Hemolysis: in patients with G6PD deficiency.

Precautions & Warnings

Mannitol should be administered with careful clinical monitoring to mitigate potential risks.

  • Fluid balance monitoring: assess input and output to avoid overload.
  • Electrolyte surveillance: check serum sodium, potassium, and osmolality regularly.
  • Pulmonary status: avoid rapid infusion in patients with existing pulmonary edema.
  • Renal function: use cautiously in severe renal impairment or anuria.
  • Infusion rate: do not exceed recommended rates to prevent sudden hemodynamic changes.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Mannitol may interact with other medications, altering efficacy or safety.

Major Interactions (Avoid)

  • Loop diuretics: additive diuretic effect can cause severe electrolyte loss.
  • Nephrotoxic antibiotics (e.g., aminoglycosides): increased risk of renal injury.
  • Vasopressors: may exacerbate hemodynamic instability when combined.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: potential for enhanced hypotensive response.
  • NSAIDs: may blunt diuretic effect and affect renal perfusion.
  • Insulin: osmotic shifts can influence glucose control.
  • Antiepileptic drugs: altered plasma osmolality may affect drug levels.
  • Contrast media: cumulative osmotic load may increase renal stress.

Frequently Asked Questions

Mannitol Braun is an injectable osmotic diuretic used to lower intracranial pressure, promote diuresis in acute renal failure, reduce intraocular pressure during eye surgery, and facilitate the renal elimination of certain nephrotoxic substances.

Mannitol increases plasma osmolality because it remains largely extracellular. This creates an osmotic gradient that draws water from cells and interstitial spaces into the bloodstream, expanding plasma volume, enhancing renal filtration, and decreasing pressure in confined compartments such as the brain and eye.

The dose of Mannitol Braun is determined by the prescribing clinician based on the specific indication, patient weight, renal function, and clinical response. Healthcare professionals calculate the appropriate volume and concentration for each individual case.

The safety of Mannitol Braun in pregnancy or while breastfeeding has not been definitively established. It should only be used if the potential benefits outweigh any potential risks, and the decision must be made by a qualified healthcare provider.

To order Mannitol Braun, 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 import documentation.

Mannitol is a widely used osmotic diuretic with a rapid onset of action and a well‑characterized safety profile. Compared with hypertonic saline, Mannitol provides both volume expansion and osmotic dehydration, making it preferred for acute reduction of intracranial pressure, whereas hypertonic saline is often chosen for specific electrolyte management.

Mannitol Braun should be stored at 2‑8 °C in a refrigerator, protected from light, and must not be frozen or shaken. Before use, inspect the solution for particulate matter or discoloration and allow it to reach room temperature if required for administration.

Mannitol Braun is administered intravenously by slow infusion through a dedicated line. The infusion rate and total volume are set by the prescribing clinician, and the solution should be given using aseptic technique to prevent contamination.

Serious risks include pulmonary edema, acute renal failure, severe electrolyte disturbances (especially hyponatremia or hypernatremia), and rare anaphylactic reactions. Continuous monitoring of fluid balance, renal function, and electrolytes is essential to detect these complications early.

Mannitol Braun is contraindicated in patients with anuria, severe pulmonary edema, active intracranial hemorrhage, or known hypersensitivity to mannitol. It should also be used with caution in individuals with severe renal impairment or uncontrolled electrolyte abnormalities.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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