GNH USA

Europe — EMA

Mannitol Bradex

GNH USA supplies Mannitol Bradex (Mannitol), an osmotic diuretic for reducing intracranial and intraocular pressure and promoting diuresis in renal failure.

Mannitol

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What is 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 USA 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.

What is Mannitol used for?

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.

What are the side effects of Mannitol?

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.

What precautions apply to Mannitol?

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.

What does Mannitol interact with?

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

What is Mannitol Bradex used for?+
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.
How does mannitol work in the body?+
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.
What is the usual dose of Mannitol Bradex?+
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.
Is Mannitol Bradex safe during pregnancy or breastfeeding?+
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.
How do I order Mannitol Bradex from GNH USA?+
To order Mannitol Bradex, submit an enquiry on the product page at gnh-usa.com indicating the required quantity. GNH USA 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.
How does Mannitol Bradex compare with other osmotic agents?+
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.
What are the storage and handling requirements for Mannitol Bradex?+
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.
How is Mannitol Bradex administered?+
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.
What are the most serious risks associated with Mannitol Bradex?+
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.
Who should not use Mannitol Bradex?+
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.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Mannitol
Route
Intravenous Use
Manufacturer
Bradex S.A.
Origin
EU

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