Product image of Hartmann´s Solution Fresenius Kabi (Sodium Lactate Solution, Potassium Chloride, Sodium Chloride, Calcium Chloride Dihydrate) supplied by GNH India

Hartmann´s Solution Fresenius Kabi

Active Ingredient:
Sodium Lactate Solution, Potassium Chloride, Sodium Chloride, Calcium Chloride Dihydrate
Origin:
EU

Hartmann´s Solution Fresenius Kabi (Sodium Lactate Solution, Potassium Chloride, Sodium Chloride, Calcium Chloride Dihydrate)

Hartmann’s Solution Fresenius Kabi is an intravenous electrolyte solution containing sodium lactate, potassium chloride, sodium chloride, and calcium chloride dihydrate. It is supplied as a sterile solution for injection, with the exact concentration not publicly disclosed, and is marketed in the European Union. The product is classified as a prescription‑only fluid and electrolyte replenishment used in clinical settings for volume expansion and electrolyte balance therapy.

Manufacturer / TM Owner

Fresenius Kabi S.R.O.

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Indications & Clinical Uses

Hartmann’s Solution Fresenius Kabi is indicated for clinical situations that require rapid restoration of extracellular fluid volume and electrolyte balance.

  • Fluid resuscitation in hypovolemic shock
  • Electrolyte replacement in patients with deficits of sodium, potassium, calcium, or chloride
  • Peri‑operative fluid management to maintain hemodynamic stability
  • Burn and trauma care to compensate for fluid losses
  • Treatment of metabolic acidosis when lactate can be metabolized

Side Effects

Adverse reactions to Hartmann’s Solution Fresenius Kabi are generally related to the infusion of electrolytes and the volume administered.

Common

  • Mild hypernatremia
  • Mild hyperkalemia
  • Mild hypocalcemia
  • Transient infusion site irritation
  • Mild metabolic alkalosis
  • Mild fluid overload

Serious

  • Severe hypernatremia
  • Severe hyperkalemia
  • Severe hypocalcemia
  • Anaphylactic reaction
  • Pulmonary edema
  • Cardiac arrhythmia

Precautions & Warnings

When prescribing Hartmann’s Solution Fresenius Kabi, clinicians should evaluate patient-specific factors and monitor relevant parameters to minimize risk.

  • Assess baseline electrolyte levels and renal function before initiation
  • Adjust infusion rate in patients with heart failure or pulmonary edema
  • Use caution in patients with severe liver disease due to lactate metabolism
  • Avoid rapid large-volume infusions in neonates and infants
  • Monitor acid‑base status during prolonged therapy
  • Discontinue if signs of electrolyte imbalance develop

Avoid Interactions

Hartmann’s Solution Fresenius Kabi may interact with other medications that affect electrolyte balance or fluid status.

Avoid

  • Concurrent use of high‑dose potassium supplements or potassium‑sparing diuretics
  • Simultaneous administration of calcium gluconate infusions without monitoring
  • Co‑administration with hypertonic saline solutions

Use with caution

  • Loop diuretics that may exacerbate electrolyte shifts
  • ACE inhibitors or ARBs in patients prone to hyperkalemia
  • Blood products that contain citrate, which can bind calcium

Frequently Asked Questions

It provides isotonic fluid and essential electrolytes to restore extracellular fluid volume and correct electrolyte imbalances in clinical settings.

It is used for fluid resuscitation, electrolyte replacement, peri‑operative fluid management, and care of patients with burns or major trauma.

The product is supplied as a sterile solution for injection and is administered intravenously under medical supervision.

Renal function should be evaluated before use, and infusion rates may need adjustment in patients with reduced kidney function.

Yes, the sodium lactate component can be metabolized to bicarbonate, helping to correct mild metabolic acidosis when appropriate.

Clinicians should monitor electrolyte concentrations, acid‑base status, fluid balance, and signs of volume overload.

It should be avoided in patients with known hypersensitivity to any component and used with caution in severe hypernatremia or hyperkalemia.

Common side effects include mild changes in serum sodium, potassium, or calcium levels, transient infusion site irritation, and mild fluid overload.

Serious reactions may include severe electrolyte disturbances, anaphylaxis, pulmonary edema, and cardiac arrhythmias.

Mixing with other hypertonic solutions should be avoided; compatibility should be confirmed before co‑administration.

Yes, it is classified as a prescription‑only drug in the European Union.

The ATC code for Hartmann’s Solution is B05AA02, indicating an electrolyte solution.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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