Product image of Osmosteril (Mannitol) supplied by GNH India

Osmosteril

Active Ingredient:
Mannitol
Origin:
EU

Osmosteril (Mannitol)

Mannitol, the active ingredient in Osmosteril, is an osmotic diuretic presented as a sterile powder for intravenous infusion use. It is employed to reduce intracranial pressure and promote diuresis in patients requiring renal support. GNH India supplies Osmosteril as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and transplant centres worldwide.

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

Manufacturer / TM Owner

Fresenius Kabi Deutschland Gmbh

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Indications & Clinical Uses

Osmosteril is an osmotic diuretic that acts on renal water handling and intracranial fluid dynamics.

  • Acute kidney injury: facilitates osmotic diuresis to aid fluid removal.
  • Cerebral edema: lowers intracranial pressure by drawing fluid from brain tissue.
  • Glaucoma surgery: used intra‑operatively to maintain ocular hypotony.
  • Intra‑operative renal protection: provides renal perfusion during brief periods of ischemia.
  • Hyperosmolar therapy: serves as a hyperosmolar agent in selected emergency settings.

How It Works

  • Mannitol functions as an osmotic 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 compartments into the vascular space, increasing renal filtration and promoting diuresis. The resulting volume expansion also transiently reduces cerebral edema by drawing fluid out of brain tissue.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate discomfort often reported after infusion.
  • Nausea: occasional gastrointestinal upset.
  • Electrolyte imbalance: shifts in sodium, potassium or calcium levels.
  • Transient hypotension: brief drop in blood pressure during rapid infusion.
  • Flank pain: discomfort in the kidney area.
  • Polyuria: increased urine output.

Serious or Rare Side Effects

  • Acute kidney injury: worsening renal function in susceptible patients.
  • Pulmonary edema: fluid accumulation in the lungs.
  • Severe electrolyte disturbances: hypernatremia or hyponatremia.
  • Anaphylactoid reaction: rare hypersensitivity with rash or bronchospasm.
  • Hemolysis: rare red‑cell destruction.
  • Metabolic acidosis: disturbance in acid‑base balance.

Precautions & Warnings

When using Osmosteril, clinicians should assess patient risk factors and monitor relevant parameters.

  • Renal function: evaluate baseline creatinine and glomerular filtration rate.
  • Fluid balance: track input‑output charts to avoid overload.
  • Electrolytes: monitor serum sodium, potassium and calcium levels.
  • Cardiovascular status: watch for hypotension during rapid infusion.
  • Pregnancy and lactation: consider risk‑benefit ratio before use.
  • Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Mannitol may interact with several concomitant medications, altering efficacy or safety.

Major Interactions (Avoid)

  • Loop diuretics: combined use can precipitate profound electrolyte loss.
  • Nephrotoxic antibiotics: increased risk of renal impairment.
  • Vasopressors: may reduce the intended osmotic effect on cerebral pressure.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors: potential additive effect on blood pressure.
  • Antihypertensive agents: may enhance hypotensive response.
  • Lithium: altered renal clearance may increase lithium levels.

Frequently Asked Questions

Osmosteril contains Mannitol and is used as an osmotic diuretic for indications such as acute kidney injury, cerebral edema, intra‑operative renal protection, and as a hyperosmolar agent in emergency settings. It helps remove excess fluid and lower intracranial pressure when administered under medical supervision.

Mannitol acts as an osmotic agent that increases plasma osmolality after intravenous administration. The resulting gradient draws water from cells and interstitial spaces into the bloodstream, enhancing renal filtration and producing diuresis while also reducing cerebral edema by extracting fluid from brain tissue.

The dose of Osmosteril is determined by the prescribing clinician based on the patient’s condition, weight, renal function and therapeutic goal. Healthcare professionals calculate the appropriate amount and infusion rate according to established clinical guidelines.

Mannitol crosses the placenta minimally, but its safety in pregnancy has not been fully established. Use is generally reserved for situations where the potential benefit outweighs any risk. Limited data are available for breastfeeding; caution is advised and a risk‑benefit assessment should be performed.

To order Osmosteril, 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 and any required import documentation.

Osmosteril (Mannitol) is a widely used osmotic diuretic with a well‑characterised safety profile. Compared with hypertonic saline, Mannitol provides both diuretic and osmotic effects, making it useful for renal protection and cerebral edema. Choice of agent depends on clinical context, patient tolerance and physician preference.

Osmosteril should be stored at temperatures below 25 °C, in its original sealed container, protected from moisture and direct sunlight. Reconstitute only with the diluent specified in the product label and use within the time frame recommended by the manufacturer.

Osmosteril is supplied as a sterile powder for intravenous infusion. It is reconstituted with a compatible sterile diluent, then administered by slow IV push or infusion according to the prescriber’s instructions, typically under continuous monitoring of vital signs and urine output.

Serious risks include acute kidney injury, pulmonary edema, severe electrolyte disturbances and rare anaphylactoid reactions. Patients should be closely monitored for changes in renal function, fluid balance, blood pressure and signs of hypersensitivity throughout treatment.

Osmosteril is contraindicated in patients with known hypersensitivity to Mannitol, severe renal impairment where oliguria is present, active pulmonary edema, and in those with uncontrolled electrolyte imbalances. Clinicians should evaluate each patient’s medical history before initiating therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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