Product image of Hartmann´s Solution Fresenius Kabi (Potassium Chloride, Sodium Chloride, Calcium Chloride Dihydrate, Sodium Lactate (As 50% Solution)) supplied by GNH India

Hartmann´s Solution Fresenius Kabi

Active Ingredient:
Potassium Chloride, Sodium Chloride, Calcium Chloride Dihydrate, Sodium Lactate (As 50% Solution)
Origin:
EU

Hartmann´s Solution Fresenius Kabi (Potassium Chloride, Sodium Chloride, Calcium Chloride Dihydrate, Sodium Lactate (As 50% Solution))

Hartmann's Solution Fresenius Kabi is an intravenous electrolyte solution containing potassium chloride, sodium chloride, calcium chloride dihydrate, and sodium lactate (as a 50 % solution). The product is supplied as a sterile solution for injection, with the exact concentration not publicly disclosed. It is classified as a prescription‑only IV fluid used to restore extracellular fluid volume and electrolyte balance in clinical settings across the EU healthcare environments.

Manufacturer / TM Owner

Fresenius Kabi S.R.O.

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Indications & Clinical Uses

Hartmann's Solution is indicated for situations where rapid fluid and electrolyte replacement is required, such as during surgery or acute dehydration.

  • Fluid resuscitation in patients with hypovolemia, hemorrhagic shock, or significant blood loss.
  • Electrolyte replacement to correct deficits of potassium, sodium, calcium, and lactate in acute settings.
  • Peri‑operative fluid management to maintain intravascular volume and hemodynamic stability during surgery.
  • Treatment of dehydration resulting from gastrointestinal losses, burns, or excessive sweating.
  • Support for patients on parenteral nutrition who require a balanced electrolyte composition.

Side Effects

Like all intravenous fluids, Hartmann's Solution may be associated with adverse reactions ranging from mild infusion‑site symptoms to rare but serious metabolic disturbances.

Common

  • Mild pain, burning, or irritation at the infusion site.
  • Transient increase in serum sodium or potassium levels.
  • Mild metabolic alkalosis due to lactate metabolism.
  • Slight elevation of blood calcium concentration.
  • Mild headache or dizziness during rapid infusion.
  • Temporary decrease in blood pressure (hypotension) if administered too quickly.

Serious

  • Hypernatremia or severe electrolyte imbalance.
  • Fluid overload leading to pulmonary edema.
  • Severe allergic or anaphylactic reaction.
  • Metabolic acidosis if lactate metabolism is impaired.
  • Severe hyperkalemia leading to cardiac arrhythmias.
  • Acute renal failure secondary to volume overload.

Precautions & Warnings

Clinicians should evaluate patient-specific factors before administering Hartmann's Solution to minimize risks and ensure appropriate fluid therapy.

  • Assess baseline electrolyte levels and renal function prior to infusion.
  • Adjust infusion rate in patients at risk for fluid overload or heart failure.
  • Use caution in individuals with severe liver disease due to altered lactate metabolism.
  • Avoid rapid administration in neonates and small children without weight‑based dosing.
  • Monitor blood pressure and cardiac rhythm during and after infusion.
  • Re‑evaluate serum electrolytes regularly during prolonged therapy.

Avoid Interactions

Hartmann's Solution may interact with other intravenous or oral agents that affect fluid balance, electrolytes, or acid‑base status.

Avoid

  • Concurrent administration of hypertonic saline solutions, which can cause severe hypernatremia.
  • Simultaneous infusion of calcium‑containing medications through the same line without proper flushing.
  • Co‑administration with bicarbonate solutions, which may precipitate calcium carbonate and obstruct lines.

Use with caution

  • Loop diuretics, as they may exacerbate electrolyte shifts.
  • ACE inhibitors or ARBs, which can increase the risk of hyperkalemia.
  • Blood products, requiring careful monitoring of calcium and potassium levels.
  • Insulin therapy, which can alter potassium distribution when combined with the solution.
  • Vasopressors, because rapid volume expansion can potentiate blood pressure changes.

Frequently Asked Questions

It is used to restore extracellular fluid volume and correct electrolyte imbalances by providing sodium, potassium, calcium, and lactate ions.

It is commonly given for fluid resuscitation in hypovolemia, peri‑operative management, treatment of dehydration, and as part of parenteral nutrition regimens.

The rate should be reduced and closely monitored to avoid fluid overload, and the patient’s cardiac status should be assessed frequently.

Yes, but dosing must be weight‑based and rapid administration should be avoided, especially in neonates and small children.

Baseline serum electrolytes (sodium, potassium, calcium), renal function tests, and acid‑base status are recommended.

Mild pain, burning, irritation, or a transient feeling of warmth at the site of injection are typical.

Hyperkalemia can occur, particularly if the patient has impaired renal function or is receiving other potassium‑containing therapies.

Lactate is metabolized to bicarbonate in the liver, which can help correct metabolic acidosis, but may be problematic in severe liver disease.

Mixing is generally discouraged unless compatible; separate lines and proper flushing are recommended to prevent precipitation.

Regular assessment of vital signs, fluid balance, and serum electrolytes is essential to detect shifts or overload early.

No, it is classified as a prescription‑only medication in the European Union.

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

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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